Director, Clinical Data Management — Lead Data Integrity

International Executive Service Corps

San Francisco (CA)

On-site

USD 240,000 - 275,000

Full time

14 days+
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Benefits offered by this job

Health Insurance
Disability Insurance
Holiday Pay
PTO
401(k) Match
Employee Stock Purchase Plan
Wellness Programs
Parental Leave Benefits

Job summary

Nektar Therapeutics invites applications for a Director, Clinical Data Management who will lead planning and execution of data management activities for phase trials, including CRF/eCRF design, database development, validation programming, discrepancy management, and database release.

The role oversees CROs and service providers, coordinating with Biostatistics, Clinical, and Regulatory teams to ensure accurate, efficient, and complete clinical trial data collection and high-quality deliverables.

Qualifications

  • Bachelor's degree required in clinical, biological, mathematical sciences or nursing; advanced degree preferred.
  • 13 years of pharmaceutical development experience with at least 6 years managing CROs.
  • Experience and understanding of ICH and GCP; ability to develop data management processes and training.

Responsibilities

  • Direct planning and execution of clinical trial data management activities, including CRF/eCRF design and database development.
  • Manage CROs and service providers throughout the data management lifecycle.
  • Coordinate with Biostatistics, Clinical, and Regulatory teams to ensure accurate data collection.
  • Develop data management processes and training; contribute to process improvements.

Skills

Problem solving
Communication skills
ICH/GCP knowledge
Project management
Team collaboration
Microsoft Project
MS Word
PowerPoint

Education

Bachelor's in clinical/biological/mathematical sciences or related field
Nursing qualification
Advanced degree preferred

Tools

Microsoft Project
Microsoft Word
PowerPoint

Job description

Nektar Therapeutics invites applications for a Director, Clinical Data Management who will lead planning and execution of data management activities for phase trials, including CRF/eCRF design, database development, validation programming, discrepancy management, and database release.

The role oversees CROs and service providers, coordinating with Biostatistics, Clinical, and Regulatory teams to ensure accurate, efficient, and complete clinical trial data collection and high-quality deliverables.

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