Clinical Study Coordinator

Description

Position Summary: We are seeking a Clinical Study Coordinator to lead operational and administrative activities of clinical trials, ensuring compliance with protocols and regulations. Key Highlights: 1. Comprehensive coordination of clinical trials. 2. Protocol and research data management. 3. Work environment and job stability. 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 Practices (GCP), and applicable local health regulations; implementing and monitoring organizational development, leadership, culture, and wellness 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 timelines. * 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. * Dangerous Goods Handling Certification (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 (commensurate with experience) * Statutory and above-statutory benefits from day one. * Medical expense insurance, life insurance, discounts at commercial establishments, etc. * Excellent work environment and job stability. **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)