Clinical Research Coordinator
il y a 4 semaines
Excelya: Advancing Clinical Research with Excellence
We are a people-centered Contract Research Organization (CRO) that excels with care. Our unique one-stop provider service model allows our team members to evolve through a diverse array of projects, advancing scientific, managerial, and human knowledge to improve the patient journey.
Mission and Responsibilities
Provide administrative and regulatory support for clinical trials, including protocol management, observation books, and submission documents. Manage the replenishment delivery of medical products to pharmacies, prepare and send documents to centers, and collaborate with partners and subcontractors.
Key Responsibilities
- Financial tracking and responsible exchanges with foreign CRAs for the cleaning of TMF: Validation of regulatory documents, validation of the certificate archiving, adaptation of the TMF tracker.
- Sends a list to the CRAs of the regulatory documents to be collected or corrected, assists with the finalization of closings, and deactivates pharmacist accounts.
- Bibliographic search, writing the research protocol and analysis plan, and establishing the data collection tool.
Requirements
You have one year's experience in an ARC or CTA position and speak and write a professional English. We commit to giving each team member the means to express their natural talents, develop their full potential, and invest their unique selves in our unique projects.
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