Data Manager
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.
Apply To This Job
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.
Apply To This Job