Job Summary
The Senior Clinical Research Associate plays a crucial role in the clinical research field, overseeing various aspects of clinical trials. This position requires a strong background in managing and monitoring clinical studies, ensuring compliance with regulatory requirements, and contributing to the overall success of clinical projects.
Responsibilities
- Manage and monitor clinical trials to ensure adherence to protocols, regulations, and timelines.
- Conduct site visits to assess site performance and maintain the integrity of clinical data.
- Collaborate with investigators and site staff to facilitate smooth trial execution.
- Oversee the preparation and review of study-related documentation, including informed consent forms and reporting protocols.
- Identify and resolve issues that arise during the trial process to ensure compliance and quality of data.
- Regularly communicate with project teams regarding study progress and share insights for continuous improvement.
Qualifications
- A degree in life sciences or a related field, with relevant experience in clinical research.
- Previous experience as a Clinical Research Associate, preferably in a senior role.
- In-depth knowledge of GCP, ICH guidelines, and relevant regulatory requirements.
- Strong organizational and project management skills.
- Excellent communication and interpersonal abilities.
- Ability to work independently and as part of a multidisciplinary team.
Tigermed provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.
