Chef principal des essais cliniques, IQVIA Biotech/Senior Clinical Trial Manager, IQVIA Biotech[...]

Senior Clinical Trial Manager IQVIA Biotech collaborates exclusively with biotechnology companies and emerging biopharmaceutical companies to support clinical development across all phases and therapeutic areas. IQVIA Biotech is seeking a Senior Clinical Trial Manager with oncology experience and a global perspective. Clinical Trial Managers play a vital role in the conduct of clinical trials. Working closely with clinical teams, they contribute to improving patients’ lives by accelerating the commercialization of new medicines. As a key member of the project team, the Clinical Trial Manager is responsible for conducting clinical studies to meet contractual requirements, in accordance with Standard Operating Procedures (SOPs), policies, and best practices. They ensure the successful execution of clinical trials for clients, lead clinical teams, and collaborate with project managers and other functional teams to guarantee adherence to execution requirements at every stage. Essential Functions Ensure the execution of clinical trials for assigned projects, in accordance with regulatory requirements (International Conference on Harmonisation (ICH) - Good Clinical Practice (GCP), protocol), client requirements (contract), and internal requirements (policies, standard operating procedures (SOPs), project plans). Ensure that project recruitment targets are met and implement appropriate recruitment strategies. Contribute to the development of the project risk management plan and manage clinical risks throughout its lifecycle. Ensure the quality of clinical trials by identifying quality standards and requirements, planning compliance assessment methods, and monitoring and managing clinical quality issues. Manage the clinical aspects of project funding, including the Estimate at Completion (EAC). Understand the scope of clinical delivery and develop plans for its implementation. Track and manage changes to the baseline Estimate at Completion (EAC) and identify opportunities for additional services or out‑of‑scope work. Identify and manage the project's clinical stakeholders, both internal and external, through effective communication and rigorous issue management. Collaborate with the clinical team to achieve established objectives. Report to internal and external stakeholders as required by the project. Plan the clinical team's resources and talent. Coach the clinical team at the project level to ensure its success through the implementation of high‑quality operational plans, appropriate training, and mentoring. Lead regular team meetings and communicate effectively to achieve objectives. Contribute to professional development by providing feedback to the clinical team's frontline managers on their performance against project tasks. Participate, as appropriate, in the development of the clinical delivery strategy for proposals. Participate in the preparation and presentation of proposals. Develop and present the clinical operations plan in partnership with business development and project management. May mentor and train new colleagues during their onboarding. May act as a lead clinical manager alongside other clinical managers for the execution of large‑scale international clinical trials. May participate in site visits, as required, to support project execution. Qualifications Bachelor's degree in health sciences or another scientific discipline required. 5 years of experience in clinical research/monitoring or an equivalent combination of education and experience required. Basic knowledge of project management practices and terminology required. Sound knowledge of regulatory requirements applicable to clinical research, including Good Clinical Practice (GCP) and International Conference on Harmonisation (ICH) guidelines. In‑depth knowledge of protocols and therapeutic aspects. Understanding of the financial aspects of projects. Salary The potential base pay range for this role, when annualized, is $116,300.00 - $193,800.00. The actual base pay offered may vary based on a number of factors including job‑related qualifications, location, and/or schedule (full or part‑time). Depending on the position offered, incentive plans, bonuses, and other compensation may be offered, in addition to a range of health, wellness and other benefits. EEO Statement 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, age, marital status, or any other status protected by applicable law. Accommodations for applicants with disabilities are available in all aspects of the recruitment process upon request. #J-18808-Ljbffr IQVIA