Ashutosh Jadhav

About Ashutosh Jadhav

I am licensed pharmacy graduate with knowledge in pharmaceutical sciences and clinical research. I was the Former Vice President of the Student Council at SCOP, Latur. I have experience in managing big groups of peoples, team leadership and had the opportunity to lead initiatives, manage different events.In addition to my pharmacy degree, I have completed an Advanced Training Program in Clinical Research, gaining clinical research knowledge in the following domains :Clinical Trials management: I have learned the fundamentals of designing, conducting, and managing clinical trials while adhering to ethical guidelines and regulatory standards. My expertise includes patient recruitment, protocol development, and ensuring compliance with Good Clinical Practice (GCP).Clinical Data Management: Skilled in handling and analyzing clinical data, I have gained knowledge of electronic data capture (EDC) systems, ensuring data integrity, and managing databases to support accurate and reliable trial outcomes.Pharmacovigilance: I understand the importance of monitoring and evaluating adverse drug reactions and ensuring patient safety. I have information in identifying, reporting, and managing risks associated with drug usage post-marketing.Regulatory Affairs: Knowledgeable in the regulatory requirements for drug development, approval, and marketing, I can navigate the complex processes to ensure that pharmaceutical products comply with international and local regulations.Medical Writing: Proficient in preparing scientific documents such as clinical study reports, protocols, informed consent forms, and regulatory submissions, I help ensure clear communication between research teams, regulatory bodies, and healthcare professionals.

Experience

1. Junior Data Analyst

   Cognizant

   Dec 2025 — Present · Navi Mumbai, IN

   Collecting, processing, and analyzing adverse event (AE) and safety dataPerforming data entry, validation, and quality checks in safety databasesSupporting case processing activities including ICSR review and triageAssisting in signal detection, data trend analysis, and safety reportingEnsuring compliance with regulatory guidelines Preparing and maintaining safety data documentation and reportsCollaborating with pharmacovigilance teams to ensure accurate data flowIdentifying data discrepancies and supporting corrective actions

Education

• Swami Ramanand Teerth Marathwada University

  Bachelor of Pharmacy - BPharm, Medicine