Lead Clinical Data Management for Complex Trials

Biopharma Careers; Foster City (CA); On-site; USD 136,000 - 176,000; Full time

Benefits offered by this job

Medical insurance

Stock-based incentives

Benefits package

Job summary

Gilead Sciences Inc. in Foster City, CA is seeking a Clinical Data Management (CDM) Lead. You will oversee CDM activities across studies, design CRF/eCRF, and manage vendors to ensure data quality and timely reporting.

The role requires leading CDM deliverables, ensuring regulatory compliance, and guiding teams through audits and inspections. Strong communication and project management skills are essential; travel may be required.

Qualifications

• Bachelor's or higher degree required with several years of CDM experience.
• Experience leading CDM activities and cross-functional teams preferred.
• Familiarity with FDA/EMA regulations and regulatory submissions preferred.

Responsibilities

• Lead one or more CDM studies and coordinate with cross-functional teams.
• Review study protocols and oversee data collection to meet timelines.
• Mentor junior staff and provide CDM process training.

Skills

CDM lead

data management

vendor management

cross-functional collaboration

regulatory understanding

Education

Bachelor's Degree

Master's Degree

Tools

EDC systems

CRF/eCRF design

Job description

Gilead Sciences Inc. in Foster City, CA is seeking a Clinical Data Management (CDM) Lead. You will oversee CDM activities across studies, design CRF/eCRF, and manage vendors to ensure data quality and timely reporting.

The role requires leading CDM deliverables, ensuring regulatory compliance, and guiding teams through audits and inspections. Strong communication and project management skills are essential; travel may be required.