Clinical Project Lead, Oncology

In this remote role you will serve as theprimary 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.

Key Responsibilities

Clinical Trial Delivery & Oversight

• Leadend-to-end country-level trial management, from study start-up through database lock and closeout
• Serve as theprimary contact for assigned clinical trials within your country
• Ensure delivery ofhigh-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

Site & Stakeholder Management

• Partner with CRA’s, Global Project Leads, and cross-functional teams to ensure successful study execution
• Leadsite feasibility, selection, and activation processes
• Driveinvestigator engagement and site performance, including recruitment and retention strategies

Operational Excellence & Compliance

• Monitor study progress through systems and reports; implementcorrective and preventive actions (CAPA) when needed
• Ensureinspection readiness through complete and accurate trial documentation (CTMS, eTMF)
• Overseepatient safety reporting (AEs/SAEs) within required timelines

Financial & Vendor Management

• Managecountry-level budgets, forecasting, and financial tracking
• Overseelocal vendors and site payments, ensuring timely and accurate processing

Regulatory & Quality Assurance

• Coordinateethics and regulatory submissions/approvals in collaboration with start-up teams
• Ensure compliance withlocal regulations and global standards (ICH-GCP)

What You Bring

Required Qualifications

• Bachelor’s degree inlife sciences, healthcare, or related field
• Strong knowledge ofICH-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 managingcomplex or early-phase trials
• Demonstrated ability to leadcross-functional teams and drive performance

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 - $232,800.00. 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.