Back to jobs

Lead Data Manager

Costa Rica Remote

Pay
Salary not listed in the saved posting
Work setup
Remote stated — work setup source
Listed location: Costa Rica Remote
Read the full posting
Employment
Unconfirmed
Apply at Clarioclinical

Tools in this posting

  • SAS
  • SQL
Source — Tool mentions in context
- High attention to detail and commitment to quality - Exposure to or experience with SAS and/or SQL preferred - Excellent written and verbal communication skills in English

Benefits in the posting

Full benefits wording
  • Competitive compensation
  • Comprehensive health, dental, and vision coverage
  • Retirement savings plan with company contribution
  • Paid time off and company holidays
  • Lead hiring, onboarding, training, and performance evaluation of Clinical Data Management team members
  • Partner with Business Development and Quality Assurance to support internal and external client meetings and audits
  • What We Look For
  • High attention to detail and commitment to quality
  • Exposure to or experience with SAS and/or SQL preferred
  • Excellent written and verbal communication skills in English

From the employer’s posting.

Job description

View original posting ↗

At Clario, a part of Thermo Fisher Scientific, we develop regulated technology that helps unlock better evidence and improve patient outcomes worldwide. Our data management teams play a critical role in ensuring high‑quality, compliant data delivery that supports Sponsors, clinical research, and regulatory success.

As a Lead Data Manager, you will ensure the delivery of high‑quality data to Sponsors while taking an active leadership role in developing and mentoring Clinical Data Management (CDM) staff. This role provides operational oversight, quality leadership, and cross‑functional collaboration to ensure data management activities are executed effectively across the lifecycle of clinical studies.

What We Offer

  • Competitive compensation

  • Comprehensive health, dental, and vision coverage

  • Retirement savings plan with company contribution

  • Paid time off and company holidays

What You’ll Be Doing

  • Lead hiring, onboarding, training, and performance evaluation of Clinical Data Management team members

  • Mentor and develop employees to support career growth and succession planning

  • Organize and deliver training on new systems, equipment, processes, and study requirements

  • Ensure team data management files and documentation are current, complete, and inspection‑ready

  • Support routine status meetings with Sponsors/CROs and internal stakeholders

  • Monitor productivity and quality across the CDM team

  • Develop and track key performance indicators (KPIs), including quality metrics, productivity, data delivery, and query performance

  • Conduct routine performance and quality reviews with managers, supervisors, and staff

  • Support team members in edit check setup and appropriate actioning of edit check output

  • Lead resolution of Quality Events related to study‑specific data management activities

  • Serve as the primary internal and Sponsor contact for Data Management‑related questions, issues, and concerns

  • Define and maintain Data Management Plans (DMPs) in collaboration with Sponsors, Project Management, and Account Management

  • Support development, review, and finalization of data transfer requirements in partnership with Sponsors and Clinical Data Programming teams

  • Participate in review and approval of Data Management‑owned study setup modules to ensure quality and compliance

  • Ensure high customer satisfaction through on‑time delivery, clear communication, and consistent service excellence

  • Assist in preparation of monthly reporting and provide data management metrics as required

  • Develop, review, and update Standard Operating Procedures (SOPs), Standard Work Instructions (SWIs), job descriptions, and departmental training materials

  • Partner with Business Development and Quality Assurance to support internal and external client meetings and audits

  • Maintain clear communication with Sponsors and internal teams regarding study status, timelines, and risks

  • Contribute to continuous process improvement initiatives, including workflow optimization and documentation

What We Look For

  • Bachelor’s degree in Life Sciences or a related field preferred

  • 5+ years of data management experience

  • Prior leadership or people management experience preferred

  • Proficiency with Microsoft Office applications

  • Strong organizational, interpersonal, time‑management, and problem‑solving skills

  • Ability to manage multiple priorities in a dynamic environment

  • High attention to detail and commitment to quality

  • Exposure to or experience with SAS and/or SQL preferred

  • Excellent written and verbal communication skills in English

  • Ability to collaborate effectively across cross‑functional and client‑facing teams

At Clario, a part of Thermo Fisher Scientific, our purpose is to transform lives by unlocking better evidence. It’s a cause that unites and inspires us. It’s why we come to work—and how we empower our people to make a positive impact every day. Whether you're advancing clinical science, supporting innovative technology, or collaborating with global teams, your work helps bring life‑changing therapies to patients faster.

Clario is an equal opportunity employer. Clario evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status, or any other legally protected characteristic.

Your next step

  • Have your CV and examples of relevant work ready.
  • Check the listed location, eligibility and core experience before starting.
  • Ask the employer about the salary range before committing time to the process.

Complete your application on clarioclinical.wd1.myworkdayjobs.com. The employer’s form will show what is required.

Already applied? Track this application

Source & posting history

View original posting ↗

Source notes

Source excerpts

Selected passages from the saved posting. Check the full description for conditions and exceptions.

Pay

No pay amount identified in the saved description.

Location & working pattern

Costa Rica Remote

Working pattern and location restrictions need checking in the full posting.

Work authorization

No clear work-authorization passage found. Eligibility is unconfirmed.

Status in our records
Active
First seen by us
Aug 13, 2026
Recorded sightings
83
Last seen by us
Sep 25, 2026
Employer says posted
Aug 11, 2026

These dates show when we found the listing. Check the employer’s website to confirm it is still accepting applications.

Report an error

See how this role fits your experience

Add your resume to compare the role’s scope, tools and requirements with your experience.

Find answers in the posting

AI
How answers work

AI selects complete passages from this posting. Check them for conditions and exceptions.

Uses this posting and your question. No profile needed.