Clinical Research Site Coordinator Specialist
2 weeks ago
We are seeking an experienced Clinical Research Site Coordinator to join our team at PSI CRO. This is an exciting opportunity for a highly organized and detail-oriented individual to work in a dynamic environment and contribute to the success of our clinical research projects.
About the RoleThe Clinical Research Site Coordinator will be responsible for facilitating the review and negotiation of clinical trial agreements (CTAs) and investigator grants between PSI Legal, the project team, and the study site. The successful candidate will have excellent communication and collaboration skills, with the ability to work effectively with multiple stakeholders.
Key Responsibilities- Review and negotiate site budgets and contracts.
- Facilitate the review and negotiation of CTAs and investigator grants.
- Customize and prepare contractually binding site-specific documents.
- Track CTA and investigator grant negotiation status in the Clinical Trial Management System (CTMS).
- Prepare executable versions of contracts and coordinate signature processes.
- Maintain local documentation and file executed contracts in the Trial Master File.
- College or University degree or equivalent combination of education, training, and experience.
- Minimum 12 months' experience in the clinical research industry.
- Knowledge and experience with legal documents related to clinical trial sites.
- Proficiency in MS Word, Excel, and PowerPoint.
- Ability to plan, multitask, and work in a dynamic team environment.
The estimated annual salary for this position is $62,000 - $72,000, depending on experience. Additionally, we offer a comprehensive benefits package, including health insurance, retirement savings plan, and paid time off.
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