Clinical Research Coordinator
hace 1 semana
Seeking a highly organized and detail-oriented Clinical Research Coordinator to join our international team at PSI CRO. As a key support to clinical research projects, you will be responsible for streamlining communication, maintaining systems, and managing documents and information.
Key Responsibilities:
- Act as the primary point of contact between site personnel and CRA involved in the project, assisting with query resolution and EDC completion.
- Manage site-level documentation, including pre-study testing and regulatory submissions.
- Coordinate preparation for and follow-up on site, TMF, and systems audits and inspections.
- Ensure proper safety information flow with investigative sites.
- Arrange and track initial and ongoing project training for site teams in all vendor-related systems.
- Document management and translations status review of the study.
Qualifications:
- College/University Degree in Life Sciences.
- Administrative work experience, preferably in an international setting.
- Prior experience working as CTA for CROs.
- Prior experience working in Clinical Research.
- Local regulations knowledge.
- Full working proficiency in English and Spanish.
- Proficiency in MS Office applications.
- Ability to plan and work in a dynamic team environment.
- Communication and collaboration skills.
Additional Information:
Advance your career in clinical research, coordinating a variety of tasks and learning new things while growing with the company.
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