About Me
With more than 9 years experience in clinical research phase II and III studies, observational and epidemiological studies. An innovative, multi-skilled professional having a track record of managing different functional projects of clinical studies.
Have experience in Medical Writing Clinical study protocol writing, CRF and ICF development, CTD Common Technical Documents – 2.4, 2.5 and 2.6 preparations.
Key skills: Clinical Protocol writing, CTD, SOP development, review Protocol, Inform Consent Documents and Case Report Forms for Clinical trials.
Clinical Site feasibility, pre-study audits, site selection, Site Initiation, Monitoring and Close out, Organizing IM and training programs
Therapeutic Experience: Oncology, Rheumatoid Arthritis, Ophthalmology and Diabetes Types of Studies Handled: Clinical Trials Domestic and International studies, PK in Patients and Observational Studies Epidemiological Studies.
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