
Posted a day ago
Associate Clinical Project Manager
IQVIA
Requirements
Bachelor’s degree in life sciences, 2+ years clinical research experience, Knowledge of ICH-GCP, MS Office proficiency
Skills
Clinical ResearchProject ManagementGCP
About the role
Responsibilities
- Support the delivery of clinical trials across Immuno-Oncology and Cell & Gene Therapy programs
- Contribute to study plans and oversee assigned study components
- Coordinate cross-functional teams to meet timelines and milestones
- Monitor study progress, identify risks, and drive solutions
- Ensure compliance with protocols, SOPs, and regulatory requirements (ICH-GCP)
- Support project financials, forecasting, and scope management
- Communicate updates to internal teams and clients
- Lead sub-teams or vendors as needed
Requirements
- Bachelor’s degree in life sciences or a related field
- Approximately 2+ years of clinical research experience
- Strong understanding of clinical trial processes and regulations (ICH-GCP)
- Excellent project coordination, organization, and problem-solving skills
- Strong communication and stakeholder management abilities
- Ability to manage multiple priorities in a fast-paced environment
- Proficiency with MS Office tools
Preferred Qualifications
- Experience in Cell & Gene Therapy, including CAR-T and cellular therapies
- Experience with Immunotherapy
- Background in global project management
- Experience with study start-up, initiation, and close-out
- Experience with first-in-human trials, dose escalation, or dose expansion studies
About the Company
IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors, offering agile, therapeutically aligned solutions to help bring breakthrough treatments to patients faster.
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IQVIA · Durham
