Suchithra Rachamalla

About Suchithra Rachamalla

I am a results-driven and self-motivated professional with impressive experience in the clinical research industry, with strong acumen in Pharmacovigilance, Drug Safety, and Development. During my six years of tenure with reputed companies, I have got well acquainted with performing the quality review of ICSR which includes a review of source documents and good knowledge in pharmacovigilance and ICSR case processing (data entry of ICSRs), MedDRA coding, drug coding. Expertise in creating appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters, and other required study documentation. My functional forte also comprises supporting and providing cross-functional collaboration and communications to increase the quality of data management deliverable. I have been acknowledged by senior management, in various instances, for my significant understanding of drug safety and capability in drug safety reports of interpretation & presentation of aggregate safety data. In-depth working knowledge of safety reporting and general regulatory environment in a clinical development environment. I also have impressive organizational skills and the motivation to work individually and as a team in a fast-paced and project-based environment. I am proficient in SOPs/regulations relevant to clinical research and practice standards; familiar with clinical trial management. To know more about my work experience and skills, you can connect with me, and I will be happy to discuss it. Thank you.

Experience

1. Safety Science Specialist

   Fortrea

   Apr 2023 — Present · IN

Education

• Johannes Kepler Universität Linz

  Master's degree, Chemistry and chemical technology