Contract
Posted Sep 16, 2026
70–100 an hour
Job Description
Lead Clinical Data Manager
Location: Redwood City, CA
Work Arrangement: Hybrid
A growing biotech company is seeking an experienced Lead Clinical Data Manager to support clinical development programs, with a focus on oncology studies. This individual will provide clinical data management leadership across clinical trials and work closely with Clinical Operations, Biostatistics, Medical, and external CRO partners.
Responsibilities
• Lead clinical data management activities for assigned clinical trials from study start-up through database lock.
• Provide data management oversight for Phase 3 oncology studies.
• Develop and review data management plans, CRFs, edit checks, data review specifications, and other study documentation.
• Manage and oversee clinical database development, validation, data cleaning, reconciliation, and database lock activities.
• Provide hands-on expertise with Medidata Rave EDC, including database build, testing, data review, and issue resolution.
• Partner with CROs and external vendors to ensure study timelines, data quality, and deliverables are met.
• Collaborate cross-functionally with Clinical Operations, Biostatistics, Statistical Programming, Medical, and Safety teams.
• Identify and resolve data-related issues and provide ongoing status updates to study teams.
• Support the development and implementation of data management processes and standards.
Qualifications
• Bachelor's degree in Life Sciences, Health Sciences, or a related field.
• 5+ years of clinical data management experience, preferably within biotech or pharmaceutical environments.
• Direct experience leading Phase 3 oncology clinical trials is required.
• Strong hands-on experience with Medidata Rave EDC is required.
• Experience managing CROs and external data management vendors.
• Strong understanding of clinical data management processes from study start-up through database lock.
• Excellent communication, organizational, and cross-functional collaboration skills.
• Ability to work effectively in a hybrid environment in Redwood City, CA.
Preferred
• Experience supporting multiple clinical programs or studies simultaneously.
• Experience with other clinical data systems and technologies.
• Experience working in a small or mid-sized biotech environment.
• Experience with oncology indications and complex Phase 3 trial designs.
Location: Redwood City, CA
Work Arrangement: Hybrid
A growing biotech company is seeking an experienced Lead Clinical Data Manager to support clinical development programs, with a focus on oncology studies. This individual will provide clinical data management leadership across clinical trials and work closely with Clinical Operations, Biostatistics, Medical, and external CRO partners.
Responsibilities
• Lead clinical data management activities for assigned clinical trials from study start-up through database lock.
• Provide data management oversight for Phase 3 oncology studies.
• Develop and review data management plans, CRFs, edit checks, data review specifications, and other study documentation.
• Manage and oversee clinical database development, validation, data cleaning, reconciliation, and database lock activities.
• Provide hands-on expertise with Medidata Rave EDC, including database build, testing, data review, and issue resolution.
• Partner with CROs and external vendors to ensure study timelines, data quality, and deliverables are met.
• Collaborate cross-functionally with Clinical Operations, Biostatistics, Statistical Programming, Medical, and Safety teams.
• Identify and resolve data-related issues and provide ongoing status updates to study teams.
• Support the development and implementation of data management processes and standards.
Qualifications
• Bachelor's degree in Life Sciences, Health Sciences, or a related field.
• 5+ years of clinical data management experience, preferably within biotech or pharmaceutical environments.
• Direct experience leading Phase 3 oncology clinical trials is required.
• Strong hands-on experience with Medidata Rave EDC is required.
• Experience managing CROs and external data management vendors.
• Strong understanding of clinical data management processes from study start-up through database lock.
• Excellent communication, organizational, and cross-functional collaboration skills.
• Ability to work effectively in a hybrid environment in Redwood City, CA.
Preferred
• Experience supporting multiple clinical programs or studies simultaneously.
• Experience with other clinical data systems and technologies.
• Experience working in a small or mid-sized biotech environment.
• Experience with oncology indications and complex Phase 3 trial designs.
Additional Details
- City
- Redwood City
- State
- California
- Country
- US
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