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The Senior Clinical Research Associate will be responsible for overseeing the day-to-day activities of clinical trials at JPMorgan Chase. This includes managing site relationships, ensuring compliance with regulatory requirements, and maintaining accurate records.
Key Accountabilities- Site Oversight: Conduct site selection, initiation, and monitoring visits to ensure trial integrity.
- Protocol Implementation: Administer protocol and related study training to assigned sites.
- Progress Monitoring: Track regulatory submissions, recruitment, case report form completion, and data query resolution.
- Collaboration: Work with cross-functional teams to address project needs.
To be successful in this role, you will need:
- A Bachelor's degree in a healthcare or scientific discipline or equivalent education.
- At least 4 years of on-site monitoring experience.
- Advanced proficiency in English.
- In-depth knowledge of GCP, ICH guidelines, and regulatory requirements.
- Strong organizational and time management skills.
- Excellent communication and interpersonal skills.
- Ability to work independently and as part of a team.
- Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
- Willingness to travel as required.
