Clinical Coordinator

Description

Job Summary: Coordinate, execute, and supervise all operational and administrative activities of clinical trials at the site, ensuring compliance with protocols and health regulations. Key Highlights: 1. Comprehensive coordination of clinical trials. 2. Management of protocols, data, and regulatory aspects. 3. Organizational development, leadership, and well-being. A leading Mexican company focused on the healthcare sector—specifically clinical research—is seeking a **Clinical Study Coordinator**. In this role, you will be responsible for coordinating, executing, and supervising all operational and administrative activities of clinical trials at the site—from site selection through study close-out—strictly adhering to the protocol, Good Clinical Practice (GCP) guidelines, and applicable local health regulations; implementing and monitoring organizational development, leadership, culture, and well-being programs and activities, ensuring their timely and effective execution. **Responsibilities:** * Protocol Management: Read, understand, and meticulously execute all activities described in the research protocol. * Data Management: Enter data into electronic data capture (EDC) systems and resolve discrepancies (queries) within established timeframes. * Regulatory Management: Maintain the regulatory binder and submit documents to Ethics Committees. * Supply Management: Manage inventory of investigational medicinal products and medical supplies, ensuring proper storage (cold chain, restricted access). * Visit Coordination: Host monitoring visits by the Clinical Research Associate (CRA), audits, and inspections by regulatory authorities. **Requirements:** *Education:* * Bachelor’s degree in a health-related field (Medicine, Nursing, Chemistry, Pharmacy, Biology, or related disciplines). Professional License. * *Preferred:* Specialization or Diploma in Clinical Research. *Experience:* * Minimum 1–2 years of prior experience coordinating clinical research protocols or providing hospital/clinical care under standardized protocols. *Technical Knowledge:* * Valid Good Clinical Practice (GCP) certification. * Certification in dangerous goods handling (IATA) for sample shipment. * Training in logbook management, master file maintenance, and electronic data capture (EDC) systems. **We Offer:** * Base salary: $15,000\.00 to $18,000\.00 gross *(based on experience)* * Statutory and above-statutory benefits from day one. * Medical expense insurance, life insurance, commercial establishment discounts, etc. * Excellent work environment and job stability. * Short-term career growth. **Benefits:** * Savings fund. * Discounts and preferential pricing. * Medical expense insurance. * Life insurance. **Working Hours:** \- Monday to Thursday: 8:00 AM to 5:00 PM; Friday: 8:00 AM to 2:00 PM. **Location:** * Colonia del Valle, Benito Juárez (near MB Poliforum and Eugenia Metro Station)