A Clinical Research Officer is responsible for overseeing the execution of clinical trials, ensuring they are conducted according to established protocols, regulatory guidelines, and ethical standards, by managing study sites, recruiting participants, monitoring data collection, and verifying the safety and integrity of research throughout the trial process.
Key responsibilities:
Study Design and Initiation: Collaborate with study teams to develop clinical trial protocols, including study objectives, methodology, and data collection procedures.
Site Monitoring and Oversight: Conduct regular monitoring visits to clinical trial sites to verify compliance with the study protocol and Good Clinical Practice (GCP) guidelines.
Participant Recruitment and Enrollment: Obtain informed consent from participants and ensure their understanding of the study procedures.
Reporting and Documentation: Prepare and submit clinical study reports to sponsors and regulatory agencies.
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Keyskills: clinical monitoring clinical research associates clinical trials clinical pharmacology clinical research clinical data management