Reeti S.
Clinical Research associate /home health coding/Oasis review level 4
Perform secondary desk search on clinical trials, company pipelines, and completive intelligence and analyze data to meet key business endpoints. Clinical trials database management and maintenance for simple PK/PD studies to complex clinical trials. Manual entry of Phase I-IV clinical trials and preclinical to launched drugs. Tracking novel, generic, and biosimilar drugs. You are tracking information from active studies on clinical trial.gov and EudraCT. Working in collaboration with the project management team and responsible for the completeness, timely delivery, and quality data for clinical studies. Performs spot checks for team quality and report to the QC team. Acquisition of data from the internet, Case Report Forms (CRFs) & Data Clarification Forms (DCFs), company registries, co-operative groups, PubMed database, Pharma web sites, medical centers and universities, conferences, FDA site, and EMEA site. Data summarization from clinical studies, publication in pre-reviewed journals, or presentation at professional meetings/conferences Drug database maintenance with information related to generic and brand names of the drugs, pipeline drugs, preclinical and clinical studies, mechanism of the drug, chemical name, formula, indications for pipeline drugs, marketing information of the drug and route, medium technology for which drug is being developed. Data cleaning, tracking, mergers/acquisitions, and updating the database.
Earnings and projects
An estimate from an earlier read
Earnings, last 30 days
No data since Nov 5, 2026.