Junior CRA

Description

Job Summary: Supervises and manages the execution of clinical trials, coordinating with patients, sponsors, and investigators, while ensuring regulatory compliance. Key Responsibilities: 1. Manage and supervise the execution of clinical trials 2. Facilitate communication between the sponsor and investigators 3. Coordinate the performance of paraclinical tests and diagnostic support **Job Description** ---------------------- Manage and supervise the execution of assigned clinical trials. 1\. Maintain ongoing contact with patients to schedule their study-related visits according to the study calendar they are participating in. 2\. Facilitate communication between the sponsor (Ethics Committee, INS, and other related institutions) and investigators. 3\. Coordinate with the clinical laboratory and imaging department to perform paraclinical tests and diagnostic support for research patients, in accordance with the protocol and/or investigator’s request. 6\. Serve as backup study coordinator when the principal coordinator is unable to carry out protocol-related activities. 3\. Enter data into the electronic databases for each study. 4\. Prepare documents required for submissions to regulatory authorities. 5\. Attend to study monitors, inspectors, and/or auditors of clinical trials. 6\. Select documentation for archiving or forwarding, as appropriate for each study. 11\. Maintain up-to-date the research unit’s database. 10\. Participate in updating institutional procedures and guidelines, as requested by the Head of the Research Unit. 7\. Review clinical records prior to study monitoring. 15\. Maintain inventory and control of devices and equipment arriving at the center for the development of assigned clinical trials. 19\. Supervise all activities performed by delegated staff for assigned studies (e.g., nurses, pharmacists, microbiologists, imaging technicians, investigators). 21\. Fulfill role-specific and study-related responsibilities in accordance with institutional guidelines, Good Clinical Practice (GCP), and local and international regulations. **Candidate Requirements** -------------------------- * Health professional. * 2 years of experience in academic training-related activities and 1 year in clinical research. * English proficiency level: A2; B1 desirable. * Knowledge of regulatory requirements. This position is open to persons with disabilities. **Selection Process** ------------------------ The selection process is conducted through Aira — a recruitment platform designed to enhance your application experience. To apply, you only need: 1\. Apply to the position. 2\. Check your email. 3\. Log in to Aira and respond to the requested questions and/or assessments. Then, if your profile matches our requirements, we will contact you via email (through Aira) to proceed to the in-person stage. **About Us** ------------------ Auna is a leading organization whose primary commitment is to deliver health and wellness to its members and patients. We continuously pursue innovation to provide high-quality, accessible health solutions for everyone. We operate in Peru, Colombia, and Mexico, and have over 14,500 employees. At Auna, we work with a people-centered, comprehensive healthcare model—the most important pillar of our mission. **Our Benefits** ----------------------- * Formal employment with all statutory benefits. * A mixed Health Plan for you and your eligible family members, covered at 85% (Base Plan Mapfre) and 75% (additional Corporate Auna Salud Plan). * 100% coverage under the Oncology Program for the plan holder and eligible dependents. * Corporate benefits and a discount club. * Food card, where applicable. * Half-day off on your birthday. * Study scholarship program: “Challenge Yourself with Auna”. * Recognition program.