Clinical Study Coordinator

Description

Job Summary: We are seeking a Clinical Study Coordinator for a research center, passionate about clinical research and adherence to Good Clinical Practice (GCP). Key Highlights: 1. Clinical research protocol coordination 2. Supervision of study execution in accordance with GCP and regulations 3. Team management and coordination **D&M Talento Integral is seeking a Clinical Study Coordinator in Col. Del Valle - Benito Juárez, Ciudad de México** --------------------------------------------------------------------------------------------------------------------- **Phase I, II, and III clinical research center seeks** **Clinical Study Coordinator** (Research Protocols | Demonstrable Experience) If you are passionate about clinical research, adherence to Good Clinical Practice (GCP), and protocol coordination, this opportunity is for you. **Academic Profile** * Bachelor's degree in: * + General Medicine + Pharmaceutical Chemist-Biologist + Nursing + Biological Sciences or another related Health Sciences discipline * **Mandatory** experience in protocols or clinical trials. **Required Experience** * Minimum **2 demonstrable years** in: * + Research protocols / clinical trials + Hospitals or clinical research sites **Functions and Responsibilities** * Supervise the proper execution of studies in accordance with: * + Approved protocols + Institutional policies + Good Clinical Practice (GCP) + Regulatory requirements * Coordinate all phases of the clinical research protocol. * Manage the generation, collection, and documentation of essential evidence. * Organize and track: * + Patient visits + Monitoring visits * Effective communication with: * + Research team + Patients * Management of investigational product. * Team management and coordination. **Technical Requirements** * Solid knowledge of **GCP**. * Desirable: **AITA certification** for international shipment of biological samples. * Experience in: * + Vital signs measurement + ECG + Sample collection and handling * Proficiency with clinical research platforms: * + IVRS (ALMAC, CENDUIT, CALYX, among others) + CRF (Medidata, Inform, etc.) **Key Skills** * Organization and attention to detail * Assertive communication * Task prioritization * Problem solving * Leadership and team management **We Offer** * **Salary:** $13,000 net * **Statutory benefits** starting from the 3rd month * **Working hours:** * + Monday to Thursday: 09:00 to 17:00 + Friday: 09:00 to 14:00 * **Location:** MB Poliforum **Desired Education Level:** Higher education - degree holder **Desired Experience Level:** Mid-level **Departmental Function:** Medicine / Health **Industry:** Pharmaceuticals **Skills:** * Clinical studies * Protocol management * Disease research *This vacancy originates from the Talenteca.com job board:* *https://www.talenteca.com/anuncio?j\_id\=6a05f2fb3700004b00859bec\&source\=indeed*