.EtCurae is growing! Are you interested in developing your knowledge and participating in high-impact clinical research? This vacancy is for you.EtCurae, has the genuine purpose of saving lives through the development of projects and protocols with Sponsors and Clinical Research of increasingly safer and better medicines for patients. For expansion, we are looking for talent.EtCurae in Clinical Drug Research offers comprehensive solutions with a genuine focus on quality, efficacy and ethics to save more and more lives.At EtCurae we are committed to respecting each person, so we do not accept any type of discrimination. And we maintain an open-door policy for diversity and inclusion.Our success depends on our culture focused on improving the quality of life of our patients through the synergy of our professionals aligned in the values of leadership, excellence, integrity and diversity.**Vacancy profile**:**Vacant position**: Study Coordinator Leader (Clinical Research)**Workplace**: CDMX, (it is essential that you reside in CDMX, with availability to move to different sites in CDMX, metropolitan area, State of Mexico and Querétaro).**Required studies**: Ing QFB, QFI / Lic in medicine or career to end to health sciences.**Experience**: minimum 5 years verifiable leading work teams in clinical research sites / projects of clinical research protocols in pharmaceutical or CROs or SMOs.**Required competences**:**Expertise**: Expert in Clinical Research / Clinical Trials protocols, at site level (hospital, clinic, research organizations). It requires extensive knowledge in Good Clinical Practices (ICH-GCP), as well as in national and international clinical research regulations.**Availability**: with availability of schedule for full working day from Monday to Friday.**Job** **Objective**:Lead, ensure and control that clinical research studies are complied with according to the protocol and the applicable national and international regulations in a timely manner for the successful activation of research sites.**Main responsibilities of the position**:1. Direct, plan, organize and control the processes, procedures and activities related to the generation, collection and documentation of all essential documents of clinical studies executed on the site.2. Ensure the correct handling of the documents generated during the execution of clinical trials, among all study personnel.3. Supervises and verifies the submission of the required documentation of a clinical trial to the Research Ethics Committee, Research Committee and/or Biosafety Committee, as appropriate.4. Supervise and verify the submission of the required documentation of a clinical trial to the Sponsor or the Regulatory Agency (COFEPRIS).5. Coordinate with the different areas of the research site and the study staff, to obtain the information and documentation for its timely and complete inclusion in the Master Folder of the clinical study.6