Clinical Trial Manager/Sr Clinical Trial Manager

The Clinical Trial Manager/Senior Clinical Trial Manager will oversee the planning, execution, and management of global oncology clinical trials from study start-up through close-out, supporting clinical development across Phases 1–3. This role combines strategic coordination with hands-on trial management to ensure studies meet scientific, operational, regulatory, and quality standards. You will collaborate with investigators, clinical research organizations (CROs), and specialized vendors to support effective study delivery. The position involves coordinating budgets, contracts, timelines, site activation, patient enrollment, and clinical trial materials. Working closely with cross-functional teams, you will contribute to study documentation, data quality, and ongoing process improvements. This opportunity suits an experienced clinical operations professional who thrives in a fast-paced, collaborative environment and is motivated by advancing oncology research and improving outcomes for patients.

• An undergraduate degree in life sciences or a related health profession, such as pharmacy, medicine, nursing, or allied health sciences, is preferred.

• Clinical Trial Manager: At least 5 years of relevant oncology clinical operations experience within a pharmaceutical company or CRO, including trial set-up, monitoring, and close-out for US and international Phase 1–3 studies conducted before NDA submission.

• Senior Clinical Trial Manager: At least 7 years of relevant oncology clinical operations experience, including trial set-up, monitoring, and close-out across US and international Phase 1–3 studies conducted before NDA submission.

• Demonstrated ability to manage multiple clinical trials, projects, and competing priorities successfully.

• Experience managing clinical study vendors, including CROs, IRT providers, laboratories, and central ECG and imaging vendors.

• Practical knowledge of ICH-GCP guidelines and US and international clinical research regulations, with experience applying these requirements in trial operations.

• Experience with electronic data capture (EDC) systems and clinical data management software.

• Experience managing Clinical Research Associates and supporting clinical team development.

• Proven ability to review and assess clinical monitoring trip reports.

• Excellent written and verbal communication skills, strong organizational abilities, and effective collaboration skills.

• Ability to work successfully with global, multidisciplinary teams in an entrepreneurial, fast-paced, and dynamic environment.

• A proactive, self-directed approach, combined with intellectual curiosity, a strong learning orientation, and a commitment to science and patient outcomes.