Clinical Project Manager / Feasibility
This Clinical Project Manager / Feasibility role plays a critical role in clinical trial planning and delivery by leading feasibility activities across the continuumfrom program / protocol feasibility through country and site selection. This position combines strategic leadership, operational excellence, and cross-functional collaboration to ensure high-quality feasibility outputs that inform study planning and accelerate trial start-up.
Key Responsibilities :
- Ensure all services adhere to policies, local regulatory requirements, and ICH-GCP guidelines.
- Collaborate with Global Program Leads (GPLs), Global Trial Leads (GTLs), and study teams to execute feasibility-related objectives.
- Perform feasibility activities including : program / protocol feasibility, country and site selection, data compilation and analytics development, creation of presentation-ready slides for study teams.
- Develop integrated feasibility plans aligned with study objectives and timelines.
- Partner with analytics teams, study team members, and country contacts to deliver feasibility outputs on time and with high quality.
- Support survey distribution, follow-up, and response analysis.
- Assist with site list development, management, and communication.
- Generate content for newsletters and other communications to ensure successful execution of feasibility processes.
Advanced Responsibilities :
Act as a Global Feasibility Lead within a therapeutic area, managing a book of work autonomously.Lead end-to-end feasibility processes for assigned studies.Project Leadership Integration :
Collaborate with cross-functional teams to identify risks and implement mitigation strategies.Monitor progress against feasibility timelines and proactively communicate updates to stakeholders.Contribute to lessons learned and best practices for continuous improvement.Support staff development and mentor less experienced team members on feasibility processes.Interfaces :
Global Feasibility TA Heads, Feasibility Insights Managers, Feasibility Data Sciences, Project Management Organization, Global Clinical Operations, EBIS, ITCRO feasibility teams, investigational sites, vendors focused on study placement, protocol design, and patient recruitment / retentionEducation & Experience :
Bachelor's degree requiredMinimum 3+ years of pharmaceutical industry experience in roles such as data procurement, business development, data strategy, or similar3+ years as part of a clinical trial feasibility team at a pharma or CRODirect feasibility experience preferredAdvanced PowerPoint skills and intermediate Excel proficiencyStrong organizational skills and ability to manage multiple projectsUnderstanding of assigned therapeutic areaAbility to analyze survey results and compile insightsExcellent written and verbal communication skills, including compelling slide designProven success working within a matrix organization to deliver high-quality outputsExtensive experience in feasibility analytics interpretationIQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide. To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us. EEO Minorities / Females / Protected Veterans / Disabled