Data Manager

Description Position Summary The Global Medical Affairs Biostatistics and Data Management team plays a central role in ensuring high-quality, reliable data supports evidence generation, regulatory submissions, and post‑market activities. We are seeking a highly skilled and motivated Data Manager to establish foundational data management processes, workflows, and SOPs within Global Medical Affairs. The Data Manager will independently lead data management activities from study planning through database lock; collaborates with Disease State Science, Clinical Research Science, Biostatistics, and external vendors; ensures high-quality data delivery for global evidence-generation studies. Primary Duties Lead end-to-end data management for Medical Affairs evidence-generation projects from start-up through database lock. Develop and maintain data standards, data dictionaries, and controlled terminologies for consistency across studies. Author Data Management Plans (DMPs), CRF/eCRF specifications, and edit checks/validation plans. Ensure compliant data collection, handling, and privacy aligned with GCP, GDPR, and HIPAA. Manage data vendors and EDC providers (e.g., Medrio, REDCap, Castor, Rave), including UAT and system configuration. Perform ongoing data review, discrepancy management, and reconciliation with external data sources. Collaborate with data engineers for automated data pipeline development. Define and manage data transfer specifications and secure data pipelines with IT/Data Engineering. Track timelines/metrics, drive issue resolution, and communicate risks and mitigations to stakeholders. Deliver clean, analysis-ready datasets to Biostatistics for reports, publications, and dashboards. Support audit/inspection readiness, documentation, and CAPA as needed. Contribute to process optimization and templates to scale the GMA data management function. Champion data integrity, traceability, and documentation across all study artifacts. Collaborate cross-functionally (Medical, Clinical Ops, Regulatory, Quality) to align on study objectives and data needs. Perform all work in compliance with company quality procedures and standards. Perform other duties as assigned. Qualifications Required Education, Training, and Experience Master's degree required (Life Sciences, Statistics, Public Health, Health Informatics, or related field). 5+ years of professional related experience with clinical data management experience (Medical Affairs/observational preferred). Experience with EDC systems and SOP development (Medrio, REDCap, Castor, or Rave; DMP/SOP authoring) Preferred Experience with real‑world evidence (RWE), registries, or post-market clinical studies. Experience in the medical device/diagnostics industry. Proficiency with MedDRA and WHODrug coding. Vendor oversight experience. Familiarity with biostatistics workflows and analysis‑ready data structures. Knowledge, Skills, and Abilities (KSA) Consistently upholds and reflects the core ethical principles and values that bioMérieux promotes. Written communications, including the ability to communicate technical data in written form. Practicing time management to allocate tasks, balance priorities, and meet deadlines efficiently. Analyze data and make decisions/recommendations using data to guide decision-making and provide suggestions for improvement. Driving continuous improvement by evaluating processes and implementing necessary changes. Ability to work cross-functionally allowing for better collaboration and communication when working across teams to achieve shared objectives. Skilled in MS Office tools including Outlook, Teams, Word, and Excel; advanced skill level. EDC design/configuration; data validation planning; query management; coding; UAT/system testing; data transfer specifications; documentation control. Knowledge of

GCP, GDPR, HIPAA

; audit readiness; CAPA management; risk and issue tracking. Ability to manage competing deadlines; support publications and dashboards with Biostats.

Supplemental Data Primary systems:

Medrio, REDCap, Castor, or Rave; ePRO/eCOA platforms; code lists (MedDRA, WHODrug). File formats & integrations include

CSV/TSV, SAS

XPT, and API‑based transfers; secure data repositories. Working Conditions & Physical Requirements Ability to remain in a stationary position (sitting or standing) for prolonged periods. Ability to ascend/descend stairs, ladders, ramps. Standard office environment with extended screen time. Ability to attend early/late global meetings. No PPE requirement. No heavy lifting or machinery operation required.

Travel Requirements Domestic travel:

5% International travel: 0 The estimated salary range for this role is between $115,000-160,000. This role is eligible to receive a variable annual bonus based on company, team, and individual performance per bioMerieux's bonus program. This range may differ from ranges offered for similar positions elsewhere in the country given differences in cost of living. Actual compensation within this range is determined based on the successful candidate's experience and will be presented in writing at the time of the offer. In addition, bioMérieux offers a competitive Total Rewards package that may include:

• A choice of medical (including prescription), dental, and vision plans providing nationwide coverage and telemedicine options
• Company-Provided Life and Accidental Death Insurance
• Short and Long-Term Disability Insurance
• Retirement Plan including a generous non-discretionary employer contribution and employer match.
• Adoption Assistance
• Wellness Programs
• Employee Assistance Program
• Commuter Benefits
• Various voluntary benefit offerings
• Discount programs
• Parental leaves #LI-US