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Senior Clinical Data Manager

Job in Palo Alto, Santa Clara County, California, 94306, USA
Listing for: Meet Life Sciences
Full Time position
Listed on 2026-01-27
Job specializations:
  • IT/Tech
    Data Analyst, Data Security, Data Warehousing
Salary/Wage Range or Industry Benchmark: 150000 - 200000 USD Yearly USD 150000.00 200000.00 YEAR
Job Description & How to Apply Below

Meet Life Sciences is partnering with a late stage biotech who are seeking an experienced Senior Clinical Data Manager to join a growing clinical team based in Palo Alto, CA. This role will play a critical part in the oversight and execution of clinical data management activities across one or more clinical programs. The ideal candidate brings deep hands-on experience from the biotech, pharmaceutical, or CRO environment and thrives in a collaborative, fast-paced setting.

Key Responsibilities
  • Lead and oversee end-to-end clinical data management activities for assigned clinical trials (Phase I–III)
  • Develop and review data management plans (DMPs), CRFs, edit checks, and data validation specifications
  • Serve as the primary data management point of contact for internal stakeholders, CROs, and vendors
  • Ensure data quality, integrity, and compliance with SOPs, ICH-GCP, and regulatory requirements
  • Oversee database builds, UAT, database locks, and data transfers
  • Review and resolve data queries, discrepancies, and protocol deviations
  • Contribute to timelines, risk assessments, and continuous process improvement initiatives
  • Support inspections, audits, and regulatory submissions as needed
  • Mentor and provide guidance to junior data management team members as appropriate
Qualifications
  • 5+ years of clinical data management experience within biotech, pharmaceutical, and/or CRO environments
  • Bachelor’s degree in life sciences, health sciences, or a related field (advanced degree a plus)
  • Strong working knowledge of clinical trial processes and data management systems (e.g., EDC platforms)
  • Experience managing CROs and external vendors
  • Solid understanding of CDISC standards (SDTM/ADaM preferred)
  • Familiarity with regulatory requirements and GxP compliance
  • Excellent organizational, communication, and cross-functional collaboration skills
  • Ability to work hybrid onsite in Palo Alto, CA (local candidates only)
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Position Requirements
10+ Years work experience
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