About The Position

IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years of experience, we offer agile, therapeutically aligned solutions and trusted partnerships that help bring breakthrough treatments to patients faster. As an Associate Project Manager (APM), you’ll play a critical role in delivering clinical trials that bring innovative therapies to patients faster. You’ll support project leadership, collaborate across teams, and help ensure studies are executed on time, on budget, and at the highest quality standards. This role offers strong growth potential, including opportunities to lead smaller studies.

Requirements

  • Bachelor’s degree in life sciences or related field
  • ~2+ years of clinical research experience
  • Understanding of clinical trial processes and regulations (ICH-GCP)
  • Strong project coordination, organization, and problem-solving skills
  • Excellent communication and stakeholder management abilities
  • Ability to manage multiple priorities in a fast-paced environment
  • Proficiency with MS Office tools

Nice To Haves

  • Cell & Gene Therapy, including CAR-T and cellular therapies
  • Immunotherapy
  • Global project management
  • Study start-up & initiation and study close-out
  • First-in-human trials
  • Dose escalation and dose expansion studies

Responsibilities

  • Support 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

Benefits

  • Health and welfare benefits
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