

Dynamic and dedicated professional with experience in materiovigilance and clinical research. Proven ability to adapt and work independently while ensuring participant safety and compliance with regulatory standards. Skilled in medical writing and data analysis, with a strong commitment to excellence in pharmaceutical research.
Training in medical device safety& adverse event reporting (MVPI)
Completed Good Clinical Practice (GP) training covering clinical research fundamentals, ethical guidelines, informed consent, adverse event reporting, and research protocols.
Gained knowledge of regulatory requirements, documentation, and participant safety in clinical trials.
Gained knowledge in pharmaceutical reserch and scientific writing
Consistency
Adaptability & Flexibility
Independent Work
Dedication