Senior Clinical Research Associate
4 weeks ago
Catalyst Clinical Research LLC is seeking a highly skilled Senior Clinical Research Associate to join our team. As a key member of our clinical research team, you will be responsible for monitoring clinical trial programs and managing regional clinical trial sites.
Key Responsibilities:
- Monitor clinical trials according to monitoring plans to achieve project goals.
- Conduct site evaluations, study initiations, routine monitoring, site close-outs, and FDA audit preparations.
- Develop and maintain relationships with site study staff and Catalyst clinical research personnel.
- Participate in internal and external meetings to maintain current knowledge on applicable regulations and guidelines.
- Collaborate closely with the Study Manager and Project Manager.
Requirements:
- Bachelor's degree in a science or health-related discipline or equivalent of 7 years industry experience.
- Minimum of 5 years' experience in clinical research with direct site monitoring experience with a sponsor company or CRO and 3 years of recent oncology clinical trial experience.
- Strong knowledge of clinical trial monitoring, regulatory compliance, clinical research methodology, and all applicable regulations and guidelines.
- Strong organizational and time management skills and the ability to work independently.
- Excellent communication and interpersonal skills.
- Flexibility and ability to travel routinely to meet project requirements.
Catalyst Clinical Research LLC is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.
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