- Performance of the role of Health Manager, ensuring compliance with regulations and health standards of the clinics.- Performing first level medical consultations and occupational medical certificates.- Diagnosis, treatment and follow-up of diseases, as well as health promotion and health promotion and disease prevention- Working collaboratively with other health care professionals to ensure a comprehensive approach to a comprehensive approach to patient care.

Perform blinded evaluations of clinical trial data to ensure objective and unbiased outcome assessments.Manage clinical trial data using CRF and IWRS electronic platforms, maintaining the accuracy and integrity of study data.Collaborate with clinical teams and data monitoring committees to assess trial progress while maintaining blinding protocols.Provide independent assessments of participant outcomes, ensuring high-quality data collection and compliance with trial standards.Assist in data review and final reporting, ensuring that blinded roles are upheld until trial completion.

Lead the informed consent process, ensuring participants’ full understanding of the study protocols and their rights.Conduct medical assessments to determine participant eligibility and monitor their safety throughout the trial.Develop, implement, and manage clinical research protocols in therapeutic areas such as COVID-19, vaccines, and chronic diseases.Handle adverse events, documenting and reporting them according to regulatory standards.Ensure proper documentation and data integrity, working closely with the clinical team and study sponsors.Participate in the planning and execution of investigator meetings, protocol amendments, and safety reporting.

•Coordinate Phase II and III clinical trials in therapeutic areas such as obesity, rheumatology, infectious diseases, pulmonology, and vaccines•Develop and manage research protocols, including studies on COVID-19 and vaccines•Perform required medical evaluations for participants, providing both in-person and remote follow-up•Manage adverse events and medical emergencies during studies; report and document adverse events in compliance with regulatory requirements•Manage data using CRF and IWRS electronic platforms to ensure the integrity and accuracy of collected information•Ensure compliance with local, national, and international regulations, including Good Clinical Practices (GCP)•Manage the informed consent process, ensuring participants understand all aspects of the study before their inclusion