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👑Data Leadership

Data Manager(Inhouse)_Hybrid@Ontario,Canada

ClinChoice · Ontario, Canada
// classified as
Data Leadership (Heads of data, directors, managers.)
posted
2d ago
location
Ontario, Canada
languages
c, r
tools
excel, oracle
> stack
crexceloracle
> description
<p>&nbsp;</p> <p>&nbsp;</p> <p style="line-height: 1;"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">ClinChoice is a global full-service CRO dedicated to professional development and providing an excellent work-life balance, with a quality-focused, collaborative “one-team” culture. We are looking for a dynamic person to join our in-house team as a&nbsp;<strong>Data Manager</strong><strong>&nbsp;</strong>on a permanent basis. This is a hybrid role at Ontario, Canada.&nbsp;</span></p> <p style="line-height: 1;"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">Join our team: you can be part of making a difference in peoples’ lives and experience a fulfilling and rewarding career!</span></p> <p style="line-height: 1;"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">The Data manager will be responsible for leading data management (DM) activities for clinical trials including database set up, study conduct and close-out. The Data manager will work collaboratively with a cross functional team to maintain project timelines and to deliver high quality DM deliverables. Key responsibilities may include, but are not limited to:</span></p> <ul> <li style="line-height: 1;"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">Lead Data management activities and ensure study deliverables meet timelines and quality standards.</span></li> <li style="line-height: 1;"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">Review of Clinical research documents (e.g. protocols, Case Report Forms).</span></li> <li style="line-height: 1;"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">Create and review electronic Case Report Form (eCRF) specifications.</span></li> <li style="line-height: 1;"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">Develop critical DM documents such as the Data Management Plan, Data Validation Plan, eCRF Completion Guidelines, Data Entry Guidelines and Data Review Plan. </span><br><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">Develop edit rules/checks, query logic and query messages.</span></li> <li style="line-height: 1;"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">Develop User Acceptance Testing Plan and perform testing on data entry screens and edit checks.</span></li> <li style="line-height: 1;"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">Create and provide training to the clinical team and sites.</span></li> <li style="line-height: 1;"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">Perform ongoing data review/reconciliation activities and provide metrics and patient trackers to monitor data clean up.</span></li> <li style="line-height: 1;"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">Perform database lock/unlock and freeze/unfreeze activities as appropriate for statistical review, interim analysis, and final database lock.</span></li> <li style="line-height: 1;"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">Coordinate the archiving of study databases and related documents</span></li> <li style="line-height: 1;"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">Create Data Transfer Specifications and perform external vendor reconciliation.</span></li> <li style="line-height: 1;"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">Perform SAE reconciliation.</span></li> <li style="line-height: 1;"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">Work to maintain/improve client satisfaction by ensuring high quality service, communication and management of clinical data.</span></li> </ul> <p style="line-height: 1;"><strong><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">Qualification</span></strong></p> <ul> <li><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">Bachelor’s degree in clinical/pharmacy biological/mathematical sciences or related field or nursing degree.</span></li> <li><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">Atleast 3 years data management and/or related work experience in a pharmaceutical industry.</span></li> <li><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">Working knowledge of Clinical research and clinical trial process and related regulatory requirement and terminology.</span></li> <li><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">Strong knowledge and experience in several Electronic Data capture systems such as Medidata Rave, Oracle InForm, OpenClinica and Medrio.</span></li> <li><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">Perform duties in compliance with SOPs, GCP and ICH guidelines.</span></li> <li><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">Ability to prioritize and to adapt quickly in fast-paced and changing industry conditions.</span></li> <li><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">Ability to lead a study or data management team independently.</span></li> <li><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">Proactively drive quality and efficiently to meet timelines and milestones to deliver high quality data management deliverables.</span></li> <li><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">Excellent verbal and written communication skills.</span></li> <li><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">Proficient in the use of Microsoft office(Outlook, word, excel, powerpoint, etc)</span></li> </ul> <p>&nbsp;</p> <p><strong>Open Date: 7/17/2026</strong></p> <p><strong>Close Date: 8/17/2026</strong></p> <p><em>ClinChoice Canada Inc. is proud to be an equal opportunity employer, valuing and respecting diversity.&nbsp; We are committed to inclusive, barrier-free recruitment and selection processes. We will accommodate the needs of qualified applicants under the&nbsp;Human Rights Code and the&nbsp;Accessibility for Ontarians Disabilities Act, in all aspects of the hiring process, upon request by calling + 1 (647)724-5709 x 301.&nbsp;</em></p> <p><em>We thank all applicants for their interest; however, only those being considered for an interview will be contacted. In accordance with Federal Personal Information Protection and Electronic Documents Act ("PIPEDA")&nbsp;,&nbsp;personal information is collected under the authority of the&nbsp;Act&nbsp;and will only be used for candidate selection.</em></p> <p><em><strong><span data-teams="true">#LI-TT1 #LI-Remote #Senior#Permanent</span></strong></em></p><div class="content-pay-transparency"><div class="pay-input"><div class="description"><p><span class="ui-provider a b c d e f g h i j k l m n o p q r s t u v w x y z ab ac ae af ag ah ai aj ak">The base salary pay range represents the anticipated low and high range for this position. Actual salary will vary based on various factors such as the candidate’s qualifications, skills, competencies, and proficiency for the role.&nbsp;</span></p></div><div class="title">Canada Pay Range</div><div class="pay-range"><span>$85</span><span class="divider">&mdash;</span><span>$105 CAD</span></div></div></div>