Clinical Trial Associate – Leading Biotech in Cardiac & Gene Therapy
A pioneering biotech company specializing in cardiac gene therapy is looking for a Clinical Trial Associate to join their team. This position offers the opportunity to work with breakthrough therapies focused on transforming cardiac care for patients with severe heart conditions. As part of this role, you’ll collaborate with leading experts and play an active role in the execution of high-impact clinical trials.
Role Responsibilities
A Clinical Trial Associate (CTA) plays a crucial role in the administration and coordination of clinical trials, which are research studies designed to evaluate the safety and efficacy of medical interventions such as drugs, devices, or treatment protocols. Below are the primary responsibilities and skills associated with the role:
Key Responsibilities:
Document Management:
- Maintain and organize essential trial documentation (e.g., study protocols, case report forms, informed consent forms).
Trial Coordination:
- Assist in the setup, monitoring, and closing of clinical trial sites.
Regulatory Compliance:
- Ensure the trial adheres to Good Clinical Practice (GCP) guidelines and local regulatory requirements.
Data Entry and Reporting:
- Track trial progress, including recruitment, data collection, and adverse events.
- Support the collection and verification of trial data.
Support to Clinical Research Associates (CRAs) and Study Managers:
- Provide administrative and logistical support.
Why Join?
This is a unique opportunity to be part of a mission-driven organization committed to advancing cardiac care. You’ll gain exposure to innovative therapies, enjoy significant career growth opportunities, and work within a passionate, high-impact team environment.
If you’re ready to make a difference in clinical research, apply today and contribute to the future of cardiac gene therapy!
