Associate Clinical Project Manager, Immuno-Oncology, Cell and Gene Therapy, IQVIA Biotech
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.
Overview
• 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
Qualifications
• 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
Preferred Experience
• 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
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com
IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
The potential base pay range for this role, when annualized, is $68,400.00 - $171,000.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.
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.
Overview
• 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
Qualifications
• 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
Preferred Experience
• 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
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com
IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
The potential base pay range for this role, when annualized, is $68,400.00 - $171,000.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.