Clinical Research Coordinator Intern

As a Clinical Research Coordinator based in Meerut, your role will involve managing and overseeing clinical trials, ensuring compliance with research protocols, and obtaining informed consent from participants. You will be responsible for monitoring and documenting clinical research activities, coordinating with research teams, and maintaining accurate records of all research data. Key Responsibilities: - Manage and oversee clinical trials - Ensure compliance with research protocols - Obtain informed consent from participants - Monitor and document clinical research activities - Coordinate with research teams - Maintain accurate and up-to-date records of research data Qualifications Required: - Life Science Graduate/B.Pharm/M.Pharm/B.Sc/M.Sc - Experience with Informed Consent and understanding of research ethics - Knowledge of Clinical Research protocols and guidelines - Proven Clinical Research Experience and involvement in Clinical Trials - Strong organizational and documentation skills - Excellent communication and interpersonal skills - Ability to work collaboratively with research teams - Bachelor's degree in a relevant field such as Life Sciences, Nursing, or a related discipline - Certification as a Clinical Research Professional (CCRP) or similar is a plus,