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Global Trial Operations Coordinator
3 weeks ago
The Clinical Documentation Specialist will play a critical role in supporting our global trial operations. This includes managing start-up documentation activities, generating CDAs, providing input into the feasibility questionnaire, and ensuring compliance with regulatory standards.
About the TeamYou will be working with a talented team of professionals who share your passion for delivering high-quality results. We value collaboration, innovation, and creativity, and we're committed to fostering a positive work environment that supports career growth and development.
Main Responsibilities- Develop and maintain collaborative working relationships with clinical investigator sites
- Support outsourcing activities by interfacing with operational teams and service providers
- Initiate and manage start-up documentation activities for global clinical trials
- Generate, process, track, and distribute Confidential Disclosure Agreements (CDAs)
- Bachelor's degree in legal, life science, or business administration, or equivalent experience
- 3-5 years of relevant clinical development or operational experience in pharmaceutical, biotech, CRO, or similar fields
- Strong organizational, time-management, analytical, and decision-making skills
- Effective communication skills in English, written and oral
