Umesh Kumar Email & Phone Number

Kerala, India

Chennai, Tamil Nadu, India

• Spearheaded the creation of comprehensive drug profiles by synthesizing data from diverse scientific and conference sources, and indexing for all the major and minor pharmaceutical companies ensuring inclusion of essential details such as potential drug activity, prescribing information, summary of product characteristics, regulatory updates, and clinical trial phases, providing stakeholders with a holistic view of the pharmaceutical products.• Collection, analysis, and validating clinical trial data from phase I-IV trials (efficacy), drug safety, tolerability, pharmacogenomic, and biomarker and pharmacodynamic studies from various clinical trial registries including clinicaltrial.gov, EudraCT, ICTRP, jRCT, ChiCTR, ANZCTR, CTRI, IRC etc. and update the database on ongoing clinical trials on recruitment status, expanded indications, monitored expected trial end dates, tracked participant enrollment numbers, coordinated trial locations and oversaw endpoints.• Maintained up-to-date company and drug records, indexing biological activity and technology of the drug from scientific research and journals including Nature, Science, NEJM, The Lancet, JAMA, BMJ etc.• Adding regulatory information (IND filings, NDA/BLA/ sNDA/ sBLA, and other designations such as Orphan Drug, Fast Track, etc.), out-licensing information, post-marketing studies, FDA approvals, etc.• Proficient in conducting SWOT analyses on pharmaceutical drugs offering customers a comprehensive understanding of the competitive landscape and market dynamics, enabling them to make informed strategic decisions.• Responsible for maintaining franchises for all drugs within the Forecast portfolio, ensuring accurate and timely updates to maintain data integrity.• Performing quality control checks and verification of edits made by colleagues to ensure accuracy and consistency in all deliverables.

Puducherry Area, India

• Inspect, collect, interpret, analyze, and compile both clinical and preclinical research literature for-structure-activity relationship(SAR) profiles, in-vivo animal and in-vitro studies, pharmacokinetics, toxicity, and safety studies, and in-vitro metabolic profiles for science effect being studied, assay conditions, biological material used to measure, the target studied, and their subsequent experimental results followed by summarization and transfer of this data to a reputed database.

Puducherry, India

• Providing essential information for superior systematic reviews with comprehensive, current, and evidence-based content through indexing to support information managers and pharmacovigilance in complying with the regulatory requirements of a licensed drug.• Assigning subject headings or coding that will help all the information to be retrieved in a systematic fashion enabling tracking and retrieval of drug information in the published literature.

M.Pharmacy (Pharmacology), Pharmacology, 77.52 %

Attended various lectures and conference programmes by INDIAN PHARMACEUtICAL CONGRESS, PUSHPAGIRI COLLEGE OF PHARMACY and other.

Master Of Business Administration - Mba, Data Science And Analytics

Master'S Degree, Pharmacology, 8.502

Master'S Degree, Pharmacology, 8.502

Bachelor Of Pharmacy (B.Pharm.), Pharmaceutical Sciences, 74.75%

Activities and Societies: NSS CAMP, ROAD SAFETY AWARENESS

High School, High School/Secondary Diplomas And Certificates

Activities and Societies: House Captain, Sports events.