Logo for Clario

Data Manager

Key Facts

Remote From: 
Full time
Mid-level (2-5 years)
English

Other Skills

  • Data Reporting
  • Microsoft Office
  • Non-Verbal Communication
  • Time Management
  • Organizational Skills
  • Detail Oriented
  • Prioritization
  • Social Skills
  • Problem Solving

Roles & Responsibilities

  • Bachelor’s degree in Life Sciences or a related field preferred
  • Minimum of 2 years of Data Management or related experience, preferably within a clinical research environment
  • Prior client-facing experience preferred
  • Proficiency in Microsoft Office applications

Requirements:

  • Serve as the primary internal and Sponsor contact for all Data Management questions, issues, and escalations, ensuring data integrity and timely delivery
  • Define, maintain, and communicate the Data Management Plan (DMP) in collaboration with Sponsors and internal Clinical Data Management teams
  • Determine and document standard and study-specific edit checks and data processing guidelines to ensure clean, high-quality data
  • Coordinate data transfer requirements and collaborate with SAS Programmers for data file creation, edit checks, and validation activities

Job description

Join Clario, part of Thermo Fisher Scientific, as a Data Manager within our Digital Physiology team. You will play a key role in ensuring high‑quality data is collected, processed, and delivered to Sponsors across global clinical studies. You will act as the primary point of contact for data‑related activities, working closely with internal teams, Sponsors, and CRO partners to ensure data integrity, compliance, and timely delivery.

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

  • Serve as the primary internal and Sponsor contact for all Data Management questions, issues, and escalations related to data collection, cleaning, delivery, reconciliation, timelines, and database lock

  • Define, maintain, and communicate the Data Management Plan (DMP) in collaboration with Sponsors and internal Clinical Data Management teams

  • Determine and document standard and study‑specific edit checks and data processing guidelines to ensure clean, high‑quality data

  • Collaborate with internal teams on study setup requirements, including demographics collection and visit schedule requirements

  • Lead the development, review, and finalization of data transfer requirements, including file specifications and approvals

  • Coordinate with SAS Programmers for data file creation, edit check development, and validation activities

  • Generate and deliver sample, routine, complete, and final data transfers in line with study timelines

  • Manage database lock activities with Sponsors to ensure data integrity and deliverable timelines are met

  • Act as the primary point of contact for Data Correction Requests (DCRs) and query escalation

  • Participate in the review and approval of Data Management components to ensure high‑quality study setups

  • Maintain complete and up‑to‑date Data Management documentation, including Data Management Plans, file specifications, data transfer agreements, data correction requests, and Sponsor communications

  • Identify out‑of‑scope requests and escalate to the Project Manager for Change Order processing

  • Conduct routine status meetings with Sponsors, CROs, and internal teams, including preparation of agendas and meeting minutes

  • Support monthly reporting activities by providing Data Management metrics as required

  • Deliver high levels of customer satisfaction by meeting commitments, timelines, and quality expectations

What We Look For

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

  • Minimum of 2 years of Data Management or related experience, preferably within a clinical research environment

  • Prior client‑facing experience preferred

  • Proficiency in Microsoft Office applications

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

  • Ability to manage multiple priorities in a fast‑paced, regulated environment

  • High attention to detail and commitment to data quality

  • Exposure to or experience with SAS and/or SQL is a plus

  • Knowledge of CDISC SDTM standards is a plus

  • Strong written and verbal communication skills in English

At Clario, 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, building innovative technology, or supporting our global teams, your work helps bring life-changing therapies to patients faster.

Data Manager Related jobs

Other jobs at Clario

We help you get seen. Not ignored.

We help you get seen faster — by the right people.

🚀

Auto-Apply

We apply for you — automatically and instantly.

Save time, skip forms, and stay on top of every opportunity. Because you can't get seen if you're not in the race.

AI Match Feedback

Know your real match before you apply.

Get a detailed AI assessment of your profile against each job posting. Because getting seen starts with passing the filters.

Upgrade to Premium. Apply smarter and get noticed.

Upgrade to Premium

Join thousands of professionals who got noticed and hired faster.