Clinical Project Lead, Oncology
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.
Key Responsibilities
Clinical Trial Delivery & Oversight
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
Site & Stakeholder Management
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
Operational Excellence & Compliance
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
Financial & Vendor Management
Manage country-level budgets, forecasting, and financial tracking
Oversee local vendors and site payments, ensuring timely and accurate processing
Regulatory & Quality Assurance
Coordinate ethics and regulatory submissions/approvals in collaboration with start-up teams
Ensure compliance with local regulations and global standards (ICH-GCP)
What You Bring
Required Qualifications
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
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.
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
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
Site & Stakeholder Management
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
Operational Excellence & Compliance
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
Financial & Vendor Management
Manage country-level budgets, forecasting, and financial tracking
Oversee local vendors and site payments, ensuring timely and accurate processing
Regulatory & Quality Assurance
Coordinate ethics and regulatory submissions/approvals in collaboration with start-up teams
Ensure compliance with local regulations and global standards (ICH-GCP)
What You Bring
Required Qualifications
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
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.