Clinical Project Lead, Oncology
IQVIA•Durham, NC
•$68,400 - $232,800•Remote
About The Position
In this remote role you will serve as the primary country-level leader for clinical trial delivery, ensuring studies are executed efficiently from start-up through closeout. You will oversee local trial operations, drive performance, and collaborate cross-functionally to deliver high-quality data aligned with regulatory requirements and sponsor expectations. This role is ideal for a clinical operations professional who thrives in a fast-paced, large matrixed environment and is passionate about improving patient outcomes through clinical research.
Requirements
- Bachelor’s degree in life sciences, healthcare, or related field
- Strong knowledge of ICH-GCP, regulatory requirements, and clinical trial processes
- Excellent communication and stakeholder management skills
- Proficiency in clinical systems (e.g., CTMS, eTMF)
- 3–5+ years of total trial management experience
- Experience managing complex or early-phase trials
- Demonstrated ability to lead cross-functional teams and drive performance
Responsibilities
- Lead end-to-end country-level trial management, from study start-up through database lock and closeout
- Serve as the primary contact for assigned clinical trials within your country
- Ensure delivery of high-quality, compliant data and documentation aligned with ICH-GCP, SOPs, and regulatory standards
- Contribute to site level recruitment strategy and contingency planning and implementation in partnership with other functional areas to achieve clinical research target
- Partner with CRA’s, Global Project Leads, and cross-functional teams to ensure successful study execution
- Lead site feasibility, selection, and activation processes
- Drive investigator engagement and site performance, including recruitment and retention strategies
- Monitor study progress through systems and reports; implement corrective and preventive actions (CAPA) when needed
- Ensure inspection readiness through complete and accurate trial documentation (CTMS, eTMF)
- Oversee patient safety reporting (AEs/SAEs) within required timelines
- Manage country-level budgets, forecasting, and financial tracking
- Oversee local vendors and site payments, ensuring timely and accurate processing
- Coordinate ethics and regulatory submissions/approvals in collaboration with start-up teams
- Ensure compliance with local regulations and global standards (ICH-GCP)
Benefits
- Health and welfare benefits
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What This Job Offers
Job Type
Full-time
Career Level
Senior
