About the role
Role Overview:
This position involves supporting and managing global clinical trials, ensuring timely delivery, quality, and compliance with regulatory standards. It includes overseeing trial setup, site management, and collaboration with CROs and internal teams.
Key Responsibilities
- Assist in planning, executing, and overseeing clinical trial activities to meet quality and regulatory standards.
- Maintain accurate documentation and support inspection readiness activities.
- Collaborate with CROs and stakeholders for site feasibility, activation, and management.
- Track service provider deliverables, timelines, and quality to ensure study alignment.
- Support risk management, protocol deviations, and issue resolution throughout trials.
- Contribute to data review, performance tracking, and reporting.
- Build strong relationships within a global, matrixed team environment.
Qualifications & Skills
- Bachelor’s degree in life sciences or related field; Master’s preferred.
- 5+ years in clinical trial management within pharma or biotech.
- Solid knowledge of ICH/GCP regulations and drug development processes.
- Experience managing multi-center, global trials in complex organizations.
- Strong project management, communication, and collaboration skills.
- Oncology or therapeutic area experience is highly desirable.
This role demands a detail-oriented, innovative professional passionate about advancing cancer and serious disease treatments through science-driven clinical trials. It offers an inclusive, collaborative environment that values contributions, fosters growth, and promotes employee well-being.