[Remote] Clinical Project Manager, IQVIA Biotech
Note: The job is a remote job and is open to candidates in USA. IQVIA Biotech is a full-service CRO dedicated to serving biotech sponsors, with a focus on accelerating clinical trial delivery. The Clinical Project Manager will play a crucial role in executing clinical studies, ensuring alignment with regulatory standards and fostering client relationships to deliver high-quality outcomes.
Responsibilities
• Participate in bid defense presentations and contribute to study strategy development; may lead presentations for smaller or regional studies
• Develop and implement integrated study management plans alongside the core project team
• Lead the planning and execution of smaller or less complex regional clinical studies, optimizing speed, quality, and cost
• Serve as a primary or backup point of contact for clients, fostering strong, collaborative customer relationships
• Build, manage, and guide cross‑functional project teams, ensuring effective communication and milestone achievement
• Monitor study progress, proactively manage risks, and drive timely issue resolution
• Ensure adherence to ICH GCP, applicable local regulations, standard processes, and company policies
• Manage project financials, including forecasting, scope management, revenue optimization, and identification of acceleration opportunities
• Oversee vendor management activities when assigned
• Support team development by mentoring less experienced project team members and contributing to a culture of continuous improvement
Skills
• Bachelor's degree in Life Sciences or a related field
• 5+ years of relevant clinical research experience, including at least 1 year of project management experience
• Broad protocol and therapeutic knowledge; familiarity with the competitive landscape and ability to articulate the value of IQVIA solutions
• Excellent communication and presentation skills
• Proven leadership capabilities, including decision‑making, performance management, and cross‑functional collaboration
• Strong problem‑solving, planning, organizational, and prioritization skills
• Ability to manage conflicting priorities while maintaining quality and accuracy
• Proficiency in MS Office applications (Word, Excel, PowerPoint)
• Understanding of project financials, including budgets, forecasting, and contractual obligations
Benefits
• Incentive plans
• Bonuses
• Health and welfare
Company Overview
• IQVIA provides analytics, compliance, and management solutions to the life sciences industry. It was founded in 1982, and is headquartered in Danbury, Connecticut, USA, with a workforce of 10001+ employees. Its website is https://www.iqvia.com.
Company H1B Sponsorship
• IQVIA has a track record of offering H1B sponsorships, with 167 in 2025, 294 in 2024, 261 in 2023, 229 in 2022, 208 in 2021, 180 in 2020. Please note that this does not guarantee sponsorship for this specific role.
Apply Now
Apply Now
Responsibilities
• Participate in bid defense presentations and contribute to study strategy development; may lead presentations for smaller or regional studies
• Develop and implement integrated study management plans alongside the core project team
• Lead the planning and execution of smaller or less complex regional clinical studies, optimizing speed, quality, and cost
• Serve as a primary or backup point of contact for clients, fostering strong, collaborative customer relationships
• Build, manage, and guide cross‑functional project teams, ensuring effective communication and milestone achievement
• Monitor study progress, proactively manage risks, and drive timely issue resolution
• Ensure adherence to ICH GCP, applicable local regulations, standard processes, and company policies
• Manage project financials, including forecasting, scope management, revenue optimization, and identification of acceleration opportunities
• Oversee vendor management activities when assigned
• Support team development by mentoring less experienced project team members and contributing to a culture of continuous improvement
Skills
• Bachelor's degree in Life Sciences or a related field
• 5+ years of relevant clinical research experience, including at least 1 year of project management experience
• Broad protocol and therapeutic knowledge; familiarity with the competitive landscape and ability to articulate the value of IQVIA solutions
• Excellent communication and presentation skills
• Proven leadership capabilities, including decision‑making, performance management, and cross‑functional collaboration
• Strong problem‑solving, planning, organizational, and prioritization skills
• Ability to manage conflicting priorities while maintaining quality and accuracy
• Proficiency in MS Office applications (Word, Excel, PowerPoint)
• Understanding of project financials, including budgets, forecasting, and contractual obligations
Benefits
• Incentive plans
• Bonuses
• Health and welfare
Company Overview
• IQVIA provides analytics, compliance, and management solutions to the life sciences industry. It was founded in 1982, and is headquartered in Danbury, Connecticut, USA, with a workforce of 10001+ employees. Its website is https://www.iqvia.com.
Company H1B Sponsorship
• IQVIA has a track record of offering H1B sponsorships, with 167 in 2025, 294 in 2024, 261 in 2023, 229 in 2022, 208 in 2021, 180 in 2020. Please note that this does not guarantee sponsorship for this specific role.
Apply Now
Apply Now