Clinical Research Coordinator
4 weeks ago
Job Title: Clinical Research Coordinator
Job Summary: We are seeking a highly skilled Clinical Research Coordinator to join our team at PSI CRO. As a key member of our start-up team, you will play a crucial role in supporting clinical research projects.
Key Responsibilities:
- Review and negotiate site budgets to ensure compliance with regulatory requirements.
- Facilitate the review and negotiation of clinical trial agreements (CTAs) and investigator grants between PSI Legal, the project team, and the study site.
- Customize and prepare contractually binding site-specific documents in cooperation with PSI Legal.
- Track CTA and investigator grant negotiation status in the Clinical Trial Management System (CTMS).
- Prepare the executable version of the contract, including grants, and coordinates the signature process.
- File executed contracts in the Trial Master File and maintains local documentation.
- Liaise with the project team, translation, and legal departments on site contracting and grant negotiation matters.
Qualifications:
- College/University degree or an equivalent combination of education, training & experience.
- Minimum of 12 months experience in the clinical research industry.
- Knowledge and experience with legal documents related to clinical trial sites.
- PC skills to be able to work with MS Word, Excel and PowerPoint.
- Ability to plan, multitask and work in a dynamic team environment.
- Communication and collaboration skills.
About PSI CRO: PSI CRO is a dynamic and growing company that offers a unique opportunity to advance your career in clinical research. As a Clinical Research Coordinator, you will have the chance to work on a variety of tasks, learn new things, and grow with the company.
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