Job Description Only CV's in English will be considered We are looking for a CRA to join our team in Mexico.Here you will have the opportunity to develop yourself as a senior, trainer, mentor and leader.We are committed to develop our employees in their careers by providing tailored courses and mentoring.Responsibilities will include: Preparation, conduct, and reporting of selection, initiation, routine and closeout monitoring visits Delivering training of investigators, site staff and project teams Work with complex studies Perform CRF review, source document verification and query resolution Be responsible for site communication and management Be involved in site identification process Contact for clinical investigators,



vendors and support services in regard to study progress Participate in feasibility research Preparation and delivering of presentations at Investigator's Meetings Preparation for and attendance at company's audits; resolution of audit findings Support to Regulatory Affairs in procurement of site regulatory documents Maintenance of study-specific automated tracking systems Qualifications College/University Degree in Life Sciences; At least 2 years experience in patient care and/or health care or clinical environment Full working proficiency in English Experience in Clinical Research is a plus Availability to travel Proficiency in MS Office applications Ability to plan and work in a dynamic team environment Communication, collaboration, and problem-solving skills Additional Information If you like to train and support others on their clinical research steps, and are also looking forward to future Lead Monitor roles, this position may just be the right one for you.Advance your career in clinical research, coordinating a variety of tasks and learning new things while growing with a rapid growing company that puts its people first.

📌 Clinical Research Associate. (Xico)
🏢 PSI
📍 Xico