
Mahipal Reddy Vennela
Pharmaceutical / Bio-tech
About Mahipal Reddy Vennela:
Experienced Clinical Research professional with a strong foundation in pharmacy and public health. Proven track record of coordinating and managing clinical trials from initiation to closeout across various therapeutic areas. Skilled in recruitment, data management, regulatory compliance, site monitoring, and data analysis, ensuring adherence to GCP guidelines and study timelines. Adept at collaborating with cross-functional teams, investigators, and regulatory authorities to deliver high-quality outcomes. Committed to advancing healthcare through meticulous research and patient safety.
Experience
Experienced Clinical Research Associate with a strong background in pharmacy and public health. Skilled in coordinating and managing clinical trials, ensuring compliance with ICH-GCP, FDA, and IRB guidelines. Proficient in site monitoring, regulatory submissions, data management, patient recruitment, and AE/SAE reporting.
At MSN Pharmaceuticals, I conduct site monitoring visits, verify data accuracy in EDC systems, and ensure regulatory compliance. Previously, as a Clinical Research Coordinator at Capitol Cardiology Associates, I managed patient recruitment, data collection, and protocol adherence. At Vasavi Hospital, I coordinated multiple trials, facilitated sponsor visits, and ensured regulatory compliance.
Committed to maintaining data integrity, patient safety, and efficient clinical trial execution.
Education
Master of Public Health from the University of New Haven, with a GPA of 3.8/4.0, focused on epidemiology, biostatistics, and clinical research methods.
Doctor of Pharmacy (Pharm.D) from Jawaharlal Nehru Technological University, with a GPA of 3.7/4.0, providing a strong foundation in pharmacology, patient care, and clinical trial management.
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