Senior Manager, External Data Acquisition – Clinical Data Management
Company: Genmab
Job ID: R14744
Category: Development Operations
Location: United States / Global (Remote Option)
Work Model: Remote / Hybrid
Career Level: Senior Manager
Job Overview
Genmab is seeking a Senior Manager in External Data Acquisition within the Clinical Data Management (CDM) team. This role is responsible for strategic oversight of third-party data acquisition and integration, including data from laboratories, eCOA providers, and other technology vendors. The position ensures external data aligns with clinical trial objectives, regulatory standards, and SDTM/CDASH requirements, supporting high-quality, compliant trial execution.
This is a high-impact role for professionals with expertise in clinical data management, external vendor coordination, and regulatory-compliant data integration in oncology or other therapeutic areas.
Key Responsibilities
Strategic Leadership
Provide insights into protocol development with a focus on external data acquisition and integration.
Standardize data type specifications to meet Electronic Data Capture (EDC) and clinical trial requirements.
Develop detailed data transfer specifications for third-party data acquisition.
Ensure data transfer processes comply with CDASH and SDTM standards for efficient analysis and reporting.
Vendor and Data Oversight
Coordinate with external vendors to ensure data compatibility with Genmab clinical databases.
Oversee Data Management CROs for seamless external data transfers.
Review vendor contracts, setup specifications, and test data transfers.
Identify and resolve issues throughout the trial lifecycle proactively.
Cross-Functional Collaboration
Work closely with internal teams, including Biomarker Operations, Data Management, Data Analytics, Medical, and Statistics.
Align external data acquisition with trial timelines, quality expectations, and regulatory requirements.
Support process improvements and best practices for external data management.
Required Qualifications
Bachelor’s degree in Science, Life Sciences, or related field (advanced degree preferred).
5–8+ years of experience in clinical data management, focusing on external data in biotech/pharma.
Strong knowledge of oncology trials, EDC systems, and data transfer technical requirements.
Proficiency with CDISC standards (SDTM) and clinical data standards development.
Familiarity with GCP, SOPs, regulatory expectations, and good data management practices.
Proven project management skills, with ability to coordinate multiple vendors and internal stakeholders.
Compensation (US-Based Roles)
Salary Range: USD 124,320 – 186,480 annually
Actual salary depends on experience, qualifications, and location. Eligible positions may include discretionary bonuses and long-term incentives.
Employee Benefits
401(k) plan with 100% match on first 6% contributions
Medical, dental, and vision insurance options
Paid vacation, sick leave, holidays, and 12 weeks discretionary parental leave
Wellness programs, tuition reimbursement, and Lifestyle Spending Account
Family support programs, financial wellness tools, and emotional well-being resources
Commuter benefits
About You
Passionate about advancing Genmab’s mission and improving patient outcomes.
Technically skilled in clinical data management and external data acquisition.
Thrives in a fast-paced environment while maintaining quality, compliance, and data integrity.
Collaborative, innovative, and committed to scientific excellence.
Able to work across multiple stakeholders, teams, and global partners effectively.
About Genmab
Genmab is a global biotechnology leader dedicated to transforming patient care with innovative antibody therapeutics. With 25 years of pioneering research in next-generation antibody technology and translational science, Genmab develops breakthrough therapies for oncology and other serious diseases. Headquartered in Copenhagen, Denmark, Genmab operates across North America, Europe, and Asia-Pacific.
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