Detail-oriented professional with a background in biotechnology, seeking to leverage comprehensive knowledge of Clinical Trials, Pharmacovigilance, Clinical Data Management, BA/BE studies, GCP guidelines, and CFR regulations in a challenging role within the clinical research industry. Equipped with strong analytical skills, meticulous attention to detail, and a commitment to upholding compliance and ethical standards. Passionate about contributing to advancements in clinical research through efficient data management, regulatory adherence, and collaborative problem-solving.
I hereby declare that the information furnished above is accurate to the best of my knowledge. I take entire responsibility for the correctness of the information provided.