Anas Pathan
open to work
- Role
- Clinical Research Coordinator at Hcg Manavata Cancer Centre
- Location
- Nashik, IN
- LinkedIn followers
- 500 followers
About Anas Pathan
Holds a Bachelor\'s degree in Pharmacy. My academic background combined with Advanced Course in Pharmacovigilance and Clinical Data Management, has equipped me with good understanding of drug safety and regulatory compliance. My primary focus lies in Pharmacovigilance, where I have developed expertise in adverse event reporting, signal detection, and risk management processes. I have practical experience using industry-standard software such as Argus Safety, Medidata Rave EDC, Oracle Clinical for data management in clinical trials. I am committed to contributing to patient safety by ensuring accurate evaluation and reporting of drug-related safety data in compliance with global regulatory standards. I aim to grow within the pharmacovigilance domain and add value to organizations dedicated to advancing healthcare through safe and effective therapies.
Experience
Clinical Research Coordinator
May 2025 — Present
Study Startup Documentation with Sponsor/CRO and EC (Ethics Committee) Submission- Regulatory Affairs involvement in study startup processes- Clinical Data Management with multiple EDC platforms (Medidata Rave, Clinion, Oracle Clinical)- Performed data entry, query resolution, and subject data management- Assisted in preparing and organizing TMF (Trial Master File) and ISF (Investigator Site File) documents- Reviewed site documents for protocol and SOP compliance- Supported study startup activities and trial master file updates- Coordinated clinical trial setup and site-level activities- Maintained CRFs (Case Report Forms), study logs, and subject records- Assisted with informed consent process and patient documentation- Ensured compliance with trial protocols and regulatory standards- Maintained subject files, reports, and related study documentation
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