&lt;p&gt;&lt;strong&gt;Position Summary:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;The Principal Clinical Database Manager is responsible for the design, development, testing, implementation, maintenance and support of clinical databases and applications. Position will interface directly with the internal team (i.e. Data Management, Project Management, etc.), EDC vendor, clients and third-party vendors to gather requirements and provide status updates. Provides operational and technical training to end users and junior staff. Additionally, the Principal Clinical Database Manager may play a lead role in internal software projects that require specialized programming and/or scripting.&amp;nbsp;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Essential functions of the job include but are not limited to:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Maintains responsibility of assigned projects. Ensures on-time delivery, communicates the status of projects to internal teams and study&lt;/li&gt;
&lt;li&gt;Provides input and guidance to the design of clinical databases to the client and internal teams&lt;/li&gt;
&lt;li&gt;Builds and supports clinical databases&lt;/li&gt;
&lt;li&gt;Develops, tests, and validates programs and clinical database to support client-related projects and third-party applications.&lt;/li&gt;
&lt;li&gt;May provide system administration and advanced technical support services for internally developed applications and clinical databases, client-related projects and third-party applications&lt;/li&gt;
&lt;li&gt;Troubleshoots and resolves software and clinical database problems&lt;/li&gt;
&lt;li&gt;Develops and maintains study-specific validation documents&lt;/li&gt;
&lt;li&gt;May provide data management support for client-related projects from CRF design to post database close and archival&lt;/li&gt;
&lt;li&gt;May design, develop and validate the Company’s internal applications, client-related projects and third-party applications.&lt;/li&gt;
&lt;li&gt;Participate in software vendor selection&lt;/li&gt;
&lt;li&gt;Participate in conducting EDC demonstrations and trainings&lt;/li&gt;
&lt;li&gt;Participate in the development and maintenance of Standard Operating Procedures (SOPs) and corresponding process documentation related to data management and database management activities&lt;/li&gt;
&lt;li&gt;Provide leadership for cross-functional and organization-wide initiatives, where applicable&lt;/li&gt;
&lt;li&gt;Trains and ensures that all data management project team members have been sufficiently trained&lt;/li&gt;
&lt;li&gt;Communicate with study sponsors, vendors and project teams as needed regarding data, database or other relevant project issues&lt;/li&gt;
&lt;li&gt;Present software demonstrations/trainings, department/company training sessions, present at project meetings&lt;/li&gt;
&lt;li&gt;Provide technical guidance and advice to key senior leadership on reasonable growth and process goals to assure data quality&lt;/li&gt;
&lt;li&gt;May require some travel&lt;/li&gt;
&lt;li&gt;Perform other duties as assigned&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Qualifications:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Minimum Required:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;5+ years’ experience with strong Medidata EDC build background.&amp;nbsp;&amp;nbsp;&lt;/li&gt;
&lt;li&gt;Bachelors and/or a combination of related experience&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;&amp;nbsp;Other Required:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Proficiency in Microsoft Office: Word, Excel, PowerPoint, Outlook&lt;/li&gt;
&lt;li&gt;Able to handle a variety of clinical research tasks&lt;/li&gt;
&lt;li&gt;Excellent organizational and communication skills&lt;/li&gt;
&lt;li&gt;Professional use of the English language; both written and oral&lt;/li&gt;
&lt;li&gt;Experience in Object Oriented Programming (C#, C++, VBS, etc.…), scripting language (PERL, etc.), SAS, R, SQL&lt;/li&gt;
&lt;li&gt;Understanding of CDISC standards (CDASH, SDTM, ADaM, etc.)&lt;/li&gt;
&lt;li&gt;Experience in clinical database management system development.&lt;/li&gt;
&lt;li&gt;Experience in a clinical, scientific or healthcare discipline.&lt;/li&gt;
&lt;li&gt;Experience in utilizing various clinical database management systems&lt;/li&gt;
&lt;li&gt;Broad knowledge of drug, device and/or biologic development and effective data management practices&lt;/li&gt;
&lt;li&gt;Strong leadership and interpersonal skills&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;&amp;nbsp;Preferred:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Medidata custom function programming or C# (C-Sharp) programming experience&lt;/li&gt;
&lt;li&gt;Oracle InForm Central Designer experience&lt;/li&gt;
&lt;li&gt;Oncology and/or Orphan Drug therapeutic experience&lt;/li&gt;
&lt;li&gt;Base SAS®, SAS/STAT and SAS/ACCESS software&lt;/li&gt;
&lt;li&gt;SAS Macro programming language&lt;/li&gt;
&lt;li&gt;Advanced experience in Database Management, object-oriented programming&lt;/li&gt;
&lt;/ul&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;p&gt;Any data provided as a part of this application will be stored in accordance with our &lt;a href=&quot;https://www.precisionmedicinegrp.com/privacy-policy/&quot; target=&quot;_blank&quot;&gt;Privacy Policy&lt;/a&gt;.&lt;/p&gt;
&lt;p&gt;Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law. © 2020 Precision Medicine Group, LLC&lt;/p&gt;
&lt;p&gt;If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process, or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at &lt;a href=&quot;mailto:QuestionForHR@precisionmedicinegrp.com&quot; target=&quot;_blank&quot;&gt;QuestionForHR@precisionmedicinegrp.com&lt;/a&gt;.&lt;/p&gt;&lt;/div&gt;

Principal Clinical Database Manager

&lt;p&gt;&lt;strong&gt;Position Summary:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;The Supervisor of Operations is responsible for daily prioritizing, scheduling and coordination of activities for assigned tasks as well as supervision of the repository staff, which includes performance management.&amp;nbsp; Tactical responsibilities include daily prioritizing, scheduling and coordination of activities for assigned tasks as well as supervision of the repository staff which includes performance management.&amp;nbsp; Ensure that repository staff receive all necessary training in required protocols, use of appropriate equipment, handling of specimens and ensure that GMP/GLP/ISO and Safety regulations and standards are met and maintained.&amp;nbsp; Supervise all activities of assigned area in a manner that is consistent with the Repository mission and management philosophy by ensuring that all aspects of our procedures are followed in compliance with the Quality Management System.&amp;nbsp; This includes but is not limited to observation and quality control checks and bringing any abnormal conditions to the attention of appropriate personnel in a timely manner. Prepare routine communications and represent the organization in a professional manner.&amp;nbsp; Actively promote a professional and positive attitude and act as a role model to foster a high performance culture.&amp;nbsp; Extended work hours may be necessary in order to meet business demands.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&amp;nbsp;&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Essential functions of the job include but are not limited to:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;Training&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Pro-actively schedule a meeting regularly with direct supervisor to review challenges, staffing and employee issues and circumstances or as they occur&lt;/li&gt;
&lt;li&gt;Complete all assigned Training Assignments&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;Scheduling, Coordination &amp;amp; Lab Supervision&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Schedule and coordinate all daily activities for assigned task(s) in an efficient manner in order to achieve successful completion of assigned tasks in accordance with Standard Operating Procedures and multiple project deadlines&lt;/li&gt;
&lt;li&gt;Collaborate with other supervisors and members of management to ensure task completion contributes to overall project success and customer satisfaction&lt;/li&gt;
&lt;li&gt;Successfully train assigned repository staff members in proper operation of all protocols, appropriate equipment usage and specimen handling&lt;/li&gt;
&lt;li&gt;May perform job specific competency assessments for direct reports and complete all appropriate checklists&lt;/li&gt;
&lt;li&gt;Collaborate with other supervisors to establishing optimal lab personnel coverage among all rotation schedules for repository tasks (i.e., fresh processing, frozen processing, freezer monitoring, and inventory of incoming frozen specimens)&lt;/li&gt;
&lt;li&gt;Pro-actively monitor and order inventory and shipping supplies and maintain appropriate inventory levels&lt;/li&gt;
&lt;li&gt;Enforce GMP/GLP/ISO and Safety regulations and standards&lt;/li&gt;
&lt;li&gt;Ensure safe lab practices and work environment. Immediately report unsafe conditions and employee incidents&lt;/li&gt;
&lt;li&gt;Conduct complex problem solving as required, using all resources available&lt;/li&gt;
&lt;li&gt;Review and approve all documentation associated with daily tasks&lt;/li&gt;
&lt;li&gt;Assist in other areas as required to meet customer expectations&lt;/li&gt;
&lt;li&gt;Provide internal and external discrepancy tracking and trending information to Repository Manager(s)&lt;/li&gt;
&lt;li&gt;Correct paperwork where necessary, and any problems as capable (refer complex problems to Manager) as brought to attention by repository staff&lt;/li&gt;
&lt;li&gt;Oversee the operation of equipment in accordance with standard operating procedures&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;Communications &amp;amp; Reporting&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Supervise repository staff in keeping with expressed objectives and corporate culture, and in doing so provide a workplace where ideas are sought and considered, initiative is encouraged, success is rewarded, and employees are treated fairly, with respect and recognition&lt;/li&gt;
&lt;li&gt;Professionally and pro-actively communicate with clients and collaborators with regard to specimen tracking, incoming shipment status and withdrawal requests both internally and externally&lt;/li&gt;
&lt;li&gt;Assist in advising clients and collaborators on organization and status of withdrawal requests, incoming shipment status, and shipping procedures&lt;/li&gt;
&lt;li&gt;Coordinate staff usage with Repository Managers and other area supervisors to achieve repository goals and objectives and to meet multiple project deadlines&lt;/li&gt;
&lt;li&gt;Manage performance of assigned staff members including coaching on the floor and/or in response to situations, track performance using Performance Notes in Performance Pro including attendance/tardiness issues as well as other related performance metrics; pro-actively participate in all aspects of performance management program&lt;/li&gt;
&lt;li&gt;Conduct regular one-on-one meetings with direct reports, no less than monthly. Document and share information and issues promptly with manager and Human Resources&lt;/li&gt;
&lt;li&gt;As a member of management, lead through example as well as require adherence to policy, procedure and professional standards at all times, including interactions of direct reports outside of work and on-line&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;Miscellaneous&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Attend required in-house management and employee training seminars as scheduled&lt;/li&gt;
&lt;li&gt;Keep current on IATA Shipping Regulations and maintain certification and standards&lt;/li&gt;
&lt;li&gt;Carry out other duties/projects as assigned&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;&amp;nbsp;&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Qualifications:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&amp;nbsp;&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Minimum Required:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Bachelor’s degree or equivalent combination of education and experience&lt;/li&gt;
&lt;li&gt;3 years of relevant laboratory experience&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Other Required:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Prior supervisory, leadership or team leader experience required including training team members on new SOPs, policies and procedures&lt;/li&gt;
&lt;li&gt;Knowledge of Aseptic technique&lt;/li&gt;
&lt;li&gt;Strong leadership skills&lt;/li&gt;
&lt;li&gt;Must be able to demonstrate high performance work culture standards, manage multiple project deadlines and follow standard operating procedures&lt;/li&gt;
&lt;li&gt;Requires excellent communication, interpersonal, organizational and multi-tasking skills&lt;/li&gt;
&lt;li&gt;Strong computer skills&lt;/li&gt;
&lt;li&gt;Good judgment and discretion required&lt;/li&gt;
&lt;li&gt;Ability to lift and carry between 31-50 lbs.; Ability to lift up to 50 lbs. overhead with assistance; frequently required to sit, stand and walk for prolonged periods; occasionally required to squat, bend, stoop, push, kneel, reach and perform tasks with repetitive motion; Will be exposed to a cold freezer environment (Freezer temperatures range between -20ºC -196ºC)&lt;/li&gt;
&lt;li&gt;Must be able to read, write, speak fluently and comprehend the English language&lt;/li&gt;
&lt;/ul&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;p&gt;Any data provided as a part of this application will be stored in accordance with our &lt;a href=&quot;https://www.precisionmedicinegrp.com/privacy-policy/&quot; target=&quot;_blank&quot;&gt;Privacy Policy&lt;/a&gt;.&lt;/p&gt;
&lt;p&gt;Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law. © 2020 Precision Medicine Group, LLC&lt;/p&gt;
&lt;p&gt;If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process, or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at &lt;a href=&quot;mailto:QuestionForHR@precisionmedicinegrp.com&quot; target=&quot;_blank&quot;&gt;QuestionForHR@precisionmedicinegrp.com&lt;/a&gt;.&lt;/p&gt;&lt;/div&gt;

Supervisor, Operations (Government Biorepository)

&lt;p&gt;&lt;strong&gt;Position Summary:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Provides statistical support for all phases of clinical development. Specific responsibilities include writing and reviewing statistical sections of protocols, writing and reviewing statistical analysis plans, and developing SAS programs for tables, listings, figures and analysis datasets in accordance with Precision and/or sponsor procedures or study specific guidelines.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Essential functions of the job include but are not limited to:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Generate and/or verify randomization schedules&lt;/li&gt;
&lt;li&gt;Review statistical methods of the clinical study protocol&lt;/li&gt;
&lt;li&gt;Provide and/or verify sample size calculations&lt;/li&gt;
&lt;li&gt;Provide input into development of case report forms (CRFs)&lt;/li&gt;
&lt;li&gt;Author statistical analysis plans, including development of table, figure and listing shells.&lt;/li&gt;
&lt;li&gt;Review statistical analysis plans written by other biostatisticians&lt;/li&gt;
&lt;li&gt;Generate analysis datasets, tables, figures, and listings to support the analysis of clinical trials data using SAS.&lt;/li&gt;
&lt;li&gt;Perform quality control for statistical based SAS programs and other study documents (e.g., presentations and reports).&lt;/li&gt;
&lt;li&gt;Provide programming and statistical support to supplemental or exploratory analyses for regulatory agencies or any other internal and external ad-hoc requests.&lt;/li&gt;
&lt;li&gt;Perform statistical consulting tasks with some senior oversight&lt;/li&gt;
&lt;li&gt;Review output across programs to ensure consistency.&lt;/li&gt;
&lt;li&gt;Provide statistical analysis and reports to Data Monitoring Committees (DMCs) as the unblinded biostatistician&lt;/li&gt;
&lt;li&gt;Review statistical sections of clinical study reports&lt;/li&gt;
&lt;li&gt;Work directly with sponsors, project managers, and external vendors on statistics-related project components&lt;/li&gt;
&lt;li&gt;Interact directly with study team&lt;/li&gt;
&lt;li&gt;Interact directly with sponsors&lt;/li&gt;
&lt;li&gt;Lead all statistical activities for study within timelines&lt;/li&gt;
&lt;li&gt;Assist with budget health review on projects and review monthly invoices&lt;/li&gt;
&lt;li&gt;Perform oversight responsibilities on projects for new biostatisticians&lt;/li&gt;
&lt;li&gt;Assist with budget development and present at bid defense meetings&lt;/li&gt;
&lt;li&gt;Participate in the development and maintenance of departmental procedures and standards (templates, SOPs, WIs etc.)&lt;/li&gt;
&lt;li&gt;Review study tasks to ensure study being conducted in line with agreed budget; identify change in scope&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Qualifications:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Minimum Required:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Master&#x27;s degree or equivalent in Statistics, Biostatistics, or related field with 4+ years experience; PhD degree in Statistics, Biostatistics, or related field with 2+ years experience&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Other Required:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Experience with SAS&lt;/li&gt;
&lt;li&gt;Knowledge of industry standards such as the ICH guidelines, CDISC data structures, 21 CFR Part 11, and FDA guidelines&lt;/li&gt;
&lt;li&gt;Knowledge of advanced clinical trial design concepts and advanced statistical methodologies&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Preferred:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Experience with Oncology and rare diseases&lt;/li&gt;
&lt;li&gt;Experience with late phase and/or submissions&lt;/li&gt;
&lt;li&gt;Experience in consulting with clients on study design&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Skills: &lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Understanding of advanced clinical trial design concepts, such as non-inferiority, adaptive methods, type-I error protection, dynamic randomization, and sample size estimation in complex settings&lt;/li&gt;
&lt;li&gt;Understanding of advanced statistical methodologies applicable to clinical trials, such as survival analysis, stratified or covariate analyses, sequential methods, and strategies for handling missing data&lt;/li&gt;
&lt;li&gt;Excellent organizational skills, time management, and ability to coordinate workload and meet established deadlines.&lt;/li&gt;
&lt;li&gt;Excellent communication and interpersonal skills to effectively interface with others.&lt;/li&gt;
&lt;li&gt;Excellent problem solving skills&lt;/li&gt;
&lt;li&gt;Excellent presentation skills&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Competencies: &lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Sound judgment/decision making&lt;/li&gt;
&lt;li&gt;Ability to establish and maintain effective working relationships with coworkers, managers and clients&lt;/li&gt;
&lt;li&gt;Service oriented, accountable and flexible&lt;/li&gt;
&lt;li&gt;Competency in written and spoken English&lt;/li&gt;
&lt;li&gt;Follow applicable regulations, including FDA, ICH, and Precision Policies and Procedures&lt;/li&gt;
&lt;li&gt;At all times to promote the image of Precision, acting as an ambassador to the Company&lt;/li&gt;
&lt;li&gt;Ensure that all internal systems are routinely updated as appropriate (e.g., timesheets, expense reports, financial reports, etc.)&lt;/li&gt;
&lt;/ul&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;p&gt;Any data provided as a part of this application will be stored in accordance with our &lt;a href=&quot;https://www.precisionmedicinegrp.com/privacy-policy/&quot; target=&quot;_blank&quot;&gt;Privacy Policy&lt;/a&gt;.&lt;/p&gt;
&lt;p&gt;Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law. © 2020 Precision Medicine Group, LLC&lt;/p&gt;
&lt;p&gt;If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process, or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at &lt;a href=&quot;mailto:QuestionForHR@precisionmedicinegrp.com&quot; target=&quot;_blank&quot;&gt;QuestionForHR@precisionmedicinegrp.com&lt;/a&gt;.&lt;/p&gt;&lt;/div&gt;

Senior Biostatistician /Biostatistician II

&lt;p&gt;&lt;strong&gt;Position Summary:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;The Financial Analyst is responsible for providing financial analysis, reporting, forecasting, and budgeting support. This position will collect and analyze financial and operational data to build timely and accurate analysis that supports financial and management reporting, decision making, and facilitates operational efficiencies. You will provide business and analytical skills, work in close partnership with business leaders across the organization, have a strategic mindset and contribute to improving the forecasting processes.&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Essential&amp;nbsp;functions of the&amp;nbsp;position&amp;nbsp;include&amp;nbsp;but are not limited to:&lt;/strong&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Providing analysis, financial modeling, and decision-making support including the annual budget, periodical forecasting, and other ad-hoc analyses&lt;/li&gt;
&lt;li&gt;Assist in compiling the monthly reporting package and forecast in a timely and accurate manner&lt;/li&gt;
&lt;li&gt;Support month-end, quarter-end and year-end activities &amp;amp; ongoing reporting including analysis of revenues, backlog, costs, and margins. Prepare commentary to explain variances between actual results and/or budget or forecasts&lt;/li&gt;
&lt;li&gt;Analyze current and past trends in key performance indicators&lt;/li&gt;
&lt;li&gt;Develop and maintain management reporting and routine business analysis&lt;/li&gt;
&lt;li&gt;Prepare ad-hoc analysis and provide special project support as needed&lt;/li&gt;
&lt;li&gt;Work collaboratively with other groups, departments, and teams to collect information, analyze data, and provide financial support&lt;/li&gt;
&lt;li&gt;Navigate through the ERP system (Infor), understand how to pull appropriate data from the system and create financial / management reports&lt;/li&gt;
&lt;li&gt;Participate in the implementation of company systems that&amp;nbsp;directly impact financial reporting&lt;/li&gt;
&lt;li&gt;Other duties as assigned&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Qualifications:&lt;/strong&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;u&gt;Minimum Required:&lt;/u&gt;&lt;/strong&gt;&amp;nbsp;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Bachelor’s degree in finance, accounting or equivalent&lt;/li&gt;
&lt;li&gt;2-3 years of experience in financial analyses, P&amp;amp;L management, budgeting, forecasting, and modeling&lt;/li&gt;
&lt;li&gt;Solid understanding of Financial Reporting and Accounting principles and processes&lt;/li&gt;
&lt;li&gt;Ability to work under pressure in fast-paced environment and manage tight deadlines&lt;/li&gt;
&lt;li&gt;Detail oriented analytical skills with a high degree of accuracy&lt;/li&gt;
&lt;li&gt;Ability to work with large sets of data to understand complex models and create business insights&lt;/li&gt;
&lt;li&gt;Ability to think creatively, highly driven, and self-motivated&lt;/li&gt;
&lt;li&gt;Strong communication and presentation skills – both written and verbal&lt;/li&gt;
&lt;li&gt;Advanced proficiency with Microsoft Office, particularly Excel and PowerPoint&lt;/li&gt;
&lt;li&gt;Ability to interact with of all levels of the organization in a team environment&lt;/li&gt;
&lt;li&gt;Must be able to read, write, speak fluently, and comprehend the English language&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;u&gt;Preferred:&lt;/u&gt;&lt;/strong&gt;&amp;nbsp;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Work on-site in the Norton (MA) or Winston-Salem (NC) office 2-3 days a week&lt;/li&gt;
&lt;li&gt;Industry experience in Pharmaceuticals, Life Sciences and/or Healthcare businesses&lt;/li&gt;
&lt;li&gt;Experience with Infor/PSA and/or other sophisticated ERP platforms and BI systems&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&amp;nbsp;&lt;/strong&gt;&lt;/p&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;p&gt;Any data provided as a part of this application will be stored in accordance with our &lt;a href=&quot;https://www.precisionmedicinegrp.com/privacy-policy/&quot; target=&quot;_blank&quot;&gt;Privacy Policy&lt;/a&gt;.&lt;/p&gt;
&lt;p&gt;Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law. © 2020 Precision Medicine Group, LLC&lt;/p&gt;
&lt;p&gt;If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process, or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at &lt;a href=&quot;mailto:QuestionForHR@precisionmedicinegrp.com&quot; target=&quot;_blank&quot;&gt;QuestionForHR@precisionmedicinegrp.com&lt;/a&gt;.&lt;/p&gt;&lt;/div&gt;

Financial Analyst 

&lt;p&gt;We have current opportunities for experienced Clinical Trial Managers and Senior Clinical Trial Managers in Europe! Join our growing team.&lt;/p&gt;
&lt;p&gt;Precision for Medicine is a precision medicine CRO. Precision’s uniquely integrated offering enables the science of precision medicine by combining novel clinical trial designs, industry-leading operational and medical experts, advanced biomarker and data analytics solutions, and an unequivocal real passion for rare diseases and oncology, in addition to working across other therapeutic areas.&lt;/p&gt;
&lt;p&gt;You will be the hub of central intelligence for the studies you will be managing, and will lead CRAs and oversee all clinical aspects of your study across multiple countries, ensuring timeline adherence and scope, whilst ensuring quality delivery. We encourage high-energy, dedicated professionals who enjoy a challenge, thrive in the details and flourish in dynamic environments to explore this opportunity.&amp;nbsp;&lt;/p&gt;
&lt;p&gt;We are addressing the challenges facing the research and development of novel compounds in Oncology and are dedicated to positively impacting the health and lives of patients around the world. If you take a consultative approach to trial management, proving to be a valuable partner in the trial operational delivery process, don&#x27;t miss exploring working with us.&lt;/p&gt;
&lt;p&gt;We offer flexible location options, and remote based working.&amp;nbsp; This position can be based in one of the following countries: UK, France, Spain, Italy, Germany, Belgium, Netherlands, Poland, Hungary, Serbia. Romania, Slovakia.&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;About You:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;You love having responsibility and a say in how clinical trials are run&lt;/li&gt;
&lt;li&gt;You plan ahead, but have alternative options and a flexible approach&lt;/li&gt;
&lt;li&gt;You are client focused and&amp;nbsp;&lt;/li&gt;
&lt;li&gt;You are well organised and able to manage timelines and shifting priorities, without sacrificing quality.&lt;/li&gt;
&lt;li&gt;You communicate clearly, often and concisely and know that your role is crucial in keeping the trial running smoothly&lt;/li&gt;
&lt;li&gt;You are a master at identifying any risks that threaten projects and handle them resolutely&lt;/li&gt;
&lt;li&gt;You thrive and work with autonomy and ownership to deliver successful outcomes&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;The day-to-day role, and how we will support your continued growth:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Management and operational delivery of the clinical elements within a trial including site selection, start-up, enrollment management, site engagement and support, monitoring planning and execution, data cleaning activities and close-out&lt;/li&gt;
&lt;li&gt;Successful execution of assigned trials and ensuring completion of trial deliverables&lt;/li&gt;
&lt;li&gt;Ensure appropriate communication, regulatory documentation, and ongoing oversight of assigned trial(s) by working in close collaboration with other functional team members&lt;/li&gt;
&lt;li&gt;Mentoring and training of team members&lt;/li&gt;
&lt;li&gt;Identify challenges to study timelines/deliverables and offer creative action plans to the team/sponsor&lt;/li&gt;
&lt;li&gt;Lead CRAs as they establish relationships with their sites for high quality oversight of monitoring, regulatory, IP, site payment and overall site correspondence activities&lt;/li&gt;
&lt;li&gt;Maintain team focus on study priorities through efficient cross-functional partnerships and effective communication to achieve the highest level of client satisfaction&lt;/li&gt;
&lt;li&gt;Sr Clinical Trial Managers may be responsible for the independent clinical project delivery for small studies without an allocated Project Manager.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Qualifications:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Minimum Required:&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Bachelor’s degree or equivalent combination of education/experience in science or health-related field, including experience in the field of&amp;nbsp; oncology&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;Other Required:&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Demonstrable experience leading clinical aspects of your studies across multiple countries in a CRO / Pharma or Biotech company.&lt;/li&gt;
&lt;li&gt;Working knowledge of GCP/ICH guidelines and the clinical development process&lt;/li&gt;
&lt;li&gt;Availability for domestic and international travel including overnight stays&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;Skills:&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Demonstrated computer skills (MS Office, MS Project, PowerPoint) and software experience (CTMS, eTMF, EDC, IXRS)&lt;/li&gt;
&lt;li&gt;Demonstrated ability to develop positive working relationships with internal and external organizations&lt;/li&gt;
&lt;li&gt;Demonstrates core understanding of medical terminology and clinical trial activities as it relates to the execution of a clinical development plan&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;Competencies:&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Demonstrates mastery knowledge of ICH-GCP, meaningful Precision SOPs, and regulatory guidance, as well as the ability to implement&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;Precision medicine is revolutionizing the attack on cancer—and we are passionate about helping you harness its power. We strike tumors on a molecular level using biomarkers to link specific mutations to specific treatments. We combine deep science with deep data from advanced technological platforms, then layer on specialized expertise in the design and execution of targeted, adaptive clinical trials. Ultimately, we deliver robust insights that inform real-time decisions—and optimize the oncology development pathway.&lt;/p&gt;
&lt;div class=&quot;content-conclusion&quot;&gt;
&lt;p&gt;Any data provided as a part of this application will be stored in accordance with our&amp;nbsp;&lt;a href=&quot;https://www.precisionmedicinegrp.com/privacy-policy/&quot; target=&quot;_blank&quot;&gt;Privacy Policy&lt;/a&gt;.&lt;/p&gt;
&lt;p&gt;Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law. © 2020 Precision Medicine Group, LLC&lt;/p&gt;
&lt;p&gt;If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process, or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at&amp;nbsp;&lt;a href=&quot;mailto:QuestionForHR@precisionmedicinegrp.com&quot; target=&quot;_blank&quot;&gt;QuestionForHR@precisionmedicinegrp.com&lt;/a&gt;.&lt;/p&gt;
&lt;/div&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;p&gt;Any data provided as a part of this application will be stored in accordance with our &lt;a href=&quot;https://www.precisionmedicinegrp.com/privacy-policy/&quot; target=&quot;_blank&quot;&gt;Privacy Policy&lt;/a&gt;.&lt;/p&gt;
&lt;p&gt;Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law. © 2020 Precision Medicine Group, LLC&lt;/p&gt;
&lt;p&gt;If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process, or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at &lt;a href=&quot;mailto:QuestionForHR@precisionmedicinegrp.com&quot; target=&quot;_blank&quot;&gt;QuestionForHR@precisionmedicinegrp.com&lt;/a&gt;.&lt;/p&gt;&lt;/div&gt;

Clinical Trial Manager / Senior Clinical Trial Manager (Oncology / Rare Disease / Biopharma)

&lt;p&gt;&lt;strong&gt;Position Summary:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&amp;nbsp;&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Provides statistical support for all phases of clinical development. Specific responsibilities include writing and reviewing statistical sections of protocols, writing and reviewing statistical analysis plans, and developing SAS programs for tables, listings, figures and analysis datasets in accordance with Precision and/or sponsor procedures or study specific guidelines.&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Essential functions of the job include but are not limited to:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Generate and/or verify randomization schedules&lt;/li&gt;
&lt;li&gt;Review statistical methods of the clinical study protocol&lt;/li&gt;
&lt;li&gt;Provide and/or verify sample size calculations&lt;/li&gt;
&lt;li&gt;Provide input into development of case report forms (CRFs)&lt;/li&gt;
&lt;li&gt;Author statistical analysis plans, including development of table, figure and listing shells.&lt;/li&gt;
&lt;li&gt;Review statistical analysis plans written by other biostatisticians&lt;/li&gt;
&lt;li&gt;Generate analysis datasets, tables, figures, and listings to support the analysis of clinical trials data using SAS.&lt;/li&gt;
&lt;li&gt;Perform quality control for statistical based SAS programs and other study documents (e.g., presentations and reports).&lt;/li&gt;
&lt;li&gt;Provide programming and statistical support to supplemental or exploratory analyses for regulatory agencies or any other internal and external ad-hoc requests.&lt;/li&gt;
&lt;li&gt;Perform statistical consulting tasks with some senior oversight&lt;/li&gt;
&lt;li&gt;Review output across programs to ensure consistency.&lt;/li&gt;
&lt;li&gt;Provide statistical analysis and reports to Data Monitoring Committees (DMCs) as the unblinded biostatistician&lt;/li&gt;
&lt;li&gt;Review statistical sections of clinical study reports&lt;/li&gt;
&lt;li&gt;Work directly with sponsors, project managers, and external vendors on statistics-related project components&lt;/li&gt;
&lt;li&gt;Interact directly with study team&lt;/li&gt;
&lt;li&gt;Interact directly with sponsors&lt;/li&gt;
&lt;li&gt;Lead all statistical activities for study within timelines&lt;/li&gt;
&lt;li&gt;Assist with budget health review on projects and review monthly invoices&lt;/li&gt;
&lt;li&gt;Perform oversight responsibilities on projects for new biostatisticians&lt;/li&gt;
&lt;li&gt;Assist with budget development and present at bid defense meetings&lt;/li&gt;
&lt;li&gt;Participate in the development and maintenance of departmental procedures and standards (templates, SOPs, WIs etc.)&lt;/li&gt;
&lt;li&gt;Review study tasks to ensure study being conducted in line with agreed budget; identify change in scope&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Qualifications:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Minimum Required:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Master&#x27;s degree or equivalent in Statistics, Biostatistics, or related field with 4+ years experience; PhD degree in Statistics, Biostatistics, or related field with 2+ years experience&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Other Required:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Experience with SAS&lt;/li&gt;
&lt;li&gt;Knowledge of industry standards such as the ICH guidelines, CDISC data structures, 21 CFR Part 11, and FDA guidelines&lt;/li&gt;
&lt;li&gt;Knowledge of advanced clinical trial design concepts and advanced statistical methodologies&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Preferred:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Experience with Oncology and rare diseases&lt;/li&gt;
&lt;li&gt;Experience with late phase and/or submissions&lt;/li&gt;
&lt;li&gt;Experience in consulting with clients on study design&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Skills: &lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Understanding of advanced clinical trial design concepts, such as non-inferiority, adaptive methods, type-I error protection, dynamic randomization, and sample size estimation in complex settings&lt;/li&gt;
&lt;li&gt;Understanding of advanced statistical methodologies applicable to clinical trials, such as survival analysis, stratified or covariate analyses, sequential methods, and strategies for handling missing data&lt;/li&gt;
&lt;li&gt;Excellent organizational skills, time management, and ability to coordinate workload and meet established deadlines.&lt;/li&gt;
&lt;li&gt;Excellent communication and interpersonal skills to effectively interface with others.&lt;/li&gt;
&lt;li&gt;Excellent problem solving skills&lt;/li&gt;
&lt;li&gt;Excellent presentation skills&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Competencies: &lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Sound judgment/decision making&lt;/li&gt;
&lt;li&gt;Ability to establish and maintain effective working relationships with coworkers, managers and clients&lt;/li&gt;
&lt;li&gt;Service oriented, accountable and flexible&lt;/li&gt;
&lt;li&gt;Competency in written and spoken English&lt;/li&gt;
&lt;li&gt;Follow applicable regulations, including FDA, ICH, and Precision Policies and Procedures&lt;/li&gt;
&lt;li&gt;At all times to promote the image of Precision, acting as an ambassador to the Company&lt;/li&gt;
&lt;li&gt;Ensure that all internal systems are routinely updated as appropriate (e.g., timesheets, expense reports, financial reports, etc.)&lt;/li&gt;
&lt;/ul&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;p&gt;Any data provided as a part of this application will be stored in accordance with our &lt;a href=&quot;https://www.precisionmedicinegrp.com/privacy-policy/&quot; target=&quot;_blank&quot;&gt;Privacy Policy&lt;/a&gt;.&lt;/p&gt;
&lt;p&gt;Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law. © 2020 Precision Medicine Group, LLC&lt;/p&gt;
&lt;p&gt;If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process, or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at &lt;a href=&quot;mailto:QuestionForHR@precisionmedicinegrp.com&quot; target=&quot;_blank&quot;&gt;QuestionForHR@precisionmedicinegrp.com&lt;/a&gt;.&lt;/p&gt;&lt;/div&gt;

&lt;p&gt;&lt;strong&gt;Position Summary:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;The Project Finance Senior Analyst is viewed as a valued lab business partner by recommending action plans and providing high quality, professional and creative financial analysis to support project level profitability, financial, and operational goals. The Project Finance Senior Analyst is&amp;nbsp;responsible for partnering with business unit leaders to provide financial expertise in reporting and interpreting key drivers of operational performance, coordinate the annual budget and monthly forecasts, and providing business support for strategic plan development at segment, department and product line levels.&amp;nbsp; This position will report to the Sr. Director of Operations Finance.&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Essential functions of the job include but are not limited to: &lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Support the Sr. Director of Operations Finance in all financial areas associated with financial analyses, reporting and forecasting of business performance&lt;/li&gt;
&lt;li&gt;Analyze monthly actuals vs. budget vs. forecast as part of the lab site monthly presentation, performing variance analysis of revenues, expenses, capital expenditures, and providing financial insights to business growth trends and profitability. Offers methods and ideas based on results.&lt;/li&gt;
&lt;li&gt;Leads lab site reforecast process including monthly roll-up and waterfall of backlog to accurately forecast revenue and profitability of business units based on dynamic inputs/assumptions.&lt;/li&gt;
&lt;li&gt;Evaluates and reports on lab site and functional headcount plans, including utilization trends to optimize delivery model efficiencies. Offers methods and ideas based on results.&lt;/li&gt;
&lt;li&gt;Prepare and coordinate lab site annual budget and long-term financial model&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li&gt;Assisting in the development and implementation of tools, systems, and processes to support strategic business initiatives, defining KPIs and establishing processes for their measurement, review, and improvement.&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li&gt;Support ad hoc requests for financial analyses and other duties as assigned.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Qualifications:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;Minimum Required:&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Bachelor’s Business Administration in Accounting/Finance or related business field&lt;/li&gt;
&lt;li&gt;2-4&amp;nbsp;years prior experience in FP&amp;amp;A or financial consulting&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;Other Required:&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Systems experience: Advanced Excel skills, experience with Salesforce and reporting tools&lt;/li&gt;
&lt;li&gt;Flexibility and willing to work on multiple assignments of varying tasks with personnel at all levels of the organization&lt;/li&gt;
&lt;li&gt;Strong interpersonal and relationship building skills, and an ability to build credibility with external and internal stakeholders&lt;/li&gt;
&lt;li&gt;Self-starting attitude with a strong desire to learn and grow rapidly&lt;/li&gt;
&lt;li&gt;Willingness to extend yourself and assist other team members&lt;/li&gt;
&lt;li&gt;Possesses ethics and integrity when dealing with confidential and sensitive information&lt;/li&gt;
&lt;li&gt;Must be able to read, write, speak fluently, and comprehend the English language&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;Preferred:&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Life Sciences experience preferred&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;p&gt;Any data provided as a part of this application will be stored in accordance with our &lt;a href=&quot;https://www.precisionmedicinegrp.com/privacy-policy/&quot; target=&quot;_blank&quot;&gt;Privacy Policy&lt;/a&gt;.&lt;/p&gt;
&lt;p&gt;Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law. © 2020 Precision Medicine Group, LLC&lt;/p&gt;
&lt;p&gt;If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process, or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at &lt;a href=&quot;mailto:QuestionForHR@precisionmedicinegrp.com&quot; target=&quot;_blank&quot;&gt;QuestionForHR@precisionmedicinegrp.com&lt;/a&gt;.&lt;/p&gt;&lt;/div&gt;

Project Finance Senior Analyst 

&lt;p&gt;&lt;strong&gt;Position Summary:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;The Biorepository Technician I will assist in shipment &amp;amp; receipt, the retrieval and preservation of biological samples that arrive daily or are stored in the repository.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&amp;nbsp;&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Essential functions of the job include but are not limited to:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Monitoring of freezers:&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Respond to freezer alarms in accordance with standard operating procedures&lt;/li&gt;
&lt;li&gt;Monitor freezers, refrigerator and room temperatures as assigned by Manager&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;Receive biological samples:&amp;nbsp;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Unpack specimens and record all pertinent information in Incoming Shipment Batch and incoming folder&lt;/li&gt;
&lt;li&gt;Create a folder to house all associated paperwork&lt;/li&gt;
&lt;li&gt;Store at appropriate temperature following guidelines set by procedures&lt;/li&gt;
&lt;li&gt;Distribute confirmation of shipment receipt form if required by project&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;Receive supplies into inventory:&amp;nbsp;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Verify shipment contents against packing list&lt;/li&gt;
&lt;li&gt;Quarantine Raw Materials for release by QA department&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;Inventory of Frozen Biological Samples:&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Check information on sample vial against information provided by the study site&lt;/li&gt;
&lt;li&gt;Scan samples into data management system, BSI&lt;/li&gt;
&lt;li&gt;Correct paperwork where necessary and inform supervisor/manager of any discrepancies by generating a discrepancy report&lt;/li&gt;
&lt;li&gt;Assist in the inventory of returned specimens&lt;/li&gt;
&lt;li&gt;Aliquot frozen specimens utilizing aseptic technique&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;Retrieve Frozen Samples from Inventory and Ship:&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Pull samples according to requisition, SOP, and instructions&lt;/li&gt;
&lt;li&gt;Perform quality control verification of outgoing samples&lt;/li&gt;
&lt;li&gt;Update Outgoing Batch Record&lt;/li&gt;
&lt;li&gt;Contact receiving labs prior to shipment to confirm shipping address and ensure contact will be available to receive specimens&lt;/li&gt;
&lt;li&gt;Ship samples (dangerous and non-dangerous goods) by Commercial or local courier&lt;/li&gt;
&lt;li&gt;Complete all paperwork (link-up forms, aliquot forms, return forms or BSI data collection sheets and any other forms which may be necessary)&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;Miscellaneous:&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Label vials and shipping boxes&lt;/li&gt;
&lt;li&gt;Perform dry shipper QC&lt;/li&gt;
&lt;li&gt;Keep current on IATA Shipping Regulations and maintain certification and standards&lt;/li&gt;
&lt;li&gt;Carry out other duties/projects as assigned&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;&amp;nbsp;&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Qualifications:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&amp;nbsp;&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Minimum Required:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;High School Diploma or equivalent combination of education and experience&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Other Required:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Requires good attention to detail, excellent documentation skills and must work well in a group environment&lt;/li&gt;
&lt;li&gt;Familiarity with excel and basic functions with the program&lt;/li&gt;
&lt;li&gt;Must be a flexible agile team player who can change activities and directions quickly and respond to a variety of assignment and changing business needs&lt;/li&gt;
&lt;li&gt;Ability to lift and carry between 31-50 lbs.; Ability to lift up to 50 lbs. overhead with assistance; frequently required to sit, stand and walk for prolonged periods; occasionally required to squat, bend, stoop, push, kneel, reach and perform tasks with repetitive motion; Will be exposed to a cold freezer environment (Freezer temperatures range between -20ºC -196ºC)&lt;/li&gt;
&lt;li&gt;Must be able to read, write, speak fluently and comprehend the English language&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Preferred:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;1 year of relevant lab experience&lt;/li&gt;
&lt;li&gt;Basic laboratory skills&lt;/li&gt;
&lt;li&gt;Trained in aseptic technique&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;&amp;nbsp;&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&amp;nbsp;&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;p&gt;Any data provided as a part of this application will be stored in accordance with our &lt;a href=&quot;https://www.precisionmedicinegrp.com/privacy-policy/&quot; target=&quot;_blank&quot;&gt;Privacy Policy&lt;/a&gt;.&lt;/p&gt;
&lt;p&gt;Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law. © 2020 Precision Medicine Group, LLC&lt;/p&gt;
&lt;p&gt;If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process, or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at &lt;a href=&quot;mailto:QuestionForHR@precisionmedicinegrp.com&quot; target=&quot;_blank&quot;&gt;QuestionForHR@precisionmedicinegrp.com&lt;/a&gt;.&lt;/p&gt;&lt;/div&gt;

Find a Job in Data