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Biogen

Associate Director, Clinical Data Management

Biogen

Associate Director overseeing Clinical Data Management in a biotech company. Collaborates to ensure high-quality data flow and provides talent development.

Posted 5/21/2026full-timeRemote • California • 🇺🇸 United StatesSenior💰 $167,000 - $230,000 per yearWebsite

About the role

Key responsibilities & impact
  • Accountable for providing Data Management expertise to assigned studies and/or programs by overseeing data quality and Data Management performance.
  • Ensures consistent implementation of data collection standards, data cleaning standards, and quality plans.
  • Contribute to the strategic development of the Data Management department, including processes, technology, data standards, reporting, process improvement, and innovation, and support the implementation of related process and system enhancements.
  • Responsible for the hiring, assignment, and development of staff within direct or indirect reporting lines.
  • Provide effective coaching and mentoring to ensure consistently high levels of performance and productivity.
  • Deliver ongoing feedback, coaching, and career development support, including engagement and retention activities, to maximize staff potential.
  • Act as a point of escalation for Data Management activities by interfacing with cross-functional customers.
  • Resolve complex issues through effective problem solving and appropriate escalation to senior management.
  • Research and resolve complex issues by leveraging appropriate resources and ensuring clear, thorough communication to support departmental awareness.

Requirements

What you’ll need
  • Bachelor’s degree, preferably in a scientific discipline such as Statistics, Mathematics, Economics, Computer Science, IT, Biology, Social Science, etc.
  • 12+ years relevant work experience in the Pharmaceutical/Biotech industry, with a focus on Clinical Data Management.
  • In-depth understanding of drug development and the biopharmaceutical industry
  • Subject matter expertise in Clinical Data Management process, quality management, and data standards development
  • Robust technical experience with electronic data capture platforms (Medidata Rave preferred) and use of data review tools (elluminate preferred)
  • Strong project management skills to effectively lead and collaborate with various business functions
  • Demonstrated ability to establish effective processes and relationships with external stakeholders, including implementing process change
  • High attention to detail, including proven ability to manage competing complex priorities successfully
  • Experience supporting audits and inspections
  • Demonstrated ability to influence without authority
  • Excellent written and oral communication skills in English.

Benefits

Comp & perks
  • Medical, Dental, Vision, & Life insurances
  • Fitness & Wellness programs including a fitness reimbursement
  • Short- and Long-Term Disability insurance
  • A minimum of 15 days of paid vacation and an additional end-of-year shutdown time off (Dec 26-Dec 31)
  • Up to 12 company paid holidays + 3 paid days off for Personal Significance
  • 80 hours of sick time per calendar year
  • Paid Maternity and Parental Leave benefit
  • 401(k) program participation with company matched contributions
  • Employee stock purchase plan
  • Tuition reimbursement of up to $10,000 per calendar year
  • Employee Resource Groups participation

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills & Tools
Data Managementdata qualitydata cleaning standardsdata collection standardsprocess improvementdata standards developmentproject managementdrug developmentClinical Data Managementaudits and inspections
Soft Skills
coachingmentoringproblem solvingcommunicationinfluence without authorityattention to detailrelationship buildingperformance managementstaff developmentcross-functional collaboration