Job description
Job Summary
The Senior Clinical Research Associate plays a crucial role in driving the innovation and development of tumor therapies at Iovance Biotherapeutics. This position is integral to the clinical trial monitoring process, ensuring adherence to protocols and compliance standards while contributing to the company’s goal of achieving leadership in biotherapeutics.
Responsibilities
- Oversee and manage clinical trial activities in accordance with regulatory guidelines and protocols.
- Collaborate with cross-functional teams to ensure the successful execution of clinical studies.
- Monitor site performance, ensuring data integrity and quality throughout trial phases.
- Maintain effective communication with site personnel and project stakeholders.
- Assist in the preparation and review of study-related documents including protocols and reports.
Qualifications
- Bachelor’s degree in a relevant field, such as life sciences, or a registered nurse (RN) qualification.
- A minimum of 4 years of experience in clinical trial monitoring.
- Strong understanding of clinical research processes, SOPs, and GCP regulations.
- Excellent organizational and communication skills, with the ability to work collaboratively in a team environment.
- Proficient in using clinical data management tools and software.
