Responsible for preparation & review of clinical trial documents (Investigators Brochure, Protocol, ICD, CRF) and interpretation of clinical data and other complex information in a most acceptable quality document (Interim Report or Clinical Study Report)
Act as liaison between Scientific affairs team and Clinical Operations study team to provide highest quality Clinical trial documents.
Review and provide the scientific feedback on the essential documents related to conduct of clinical trial.
Primary point of contact for all the Medical writing in clinical trials, regulatory, marketing and Publication of designated projects
Write and review scientific abstracts, publication, related to clinical studies. Provide scientific inputs on Healthcare website, health magazine etc. Work closely with multidisciplinary group of experts to translate the study data and results into presentations, reports, regulatory documents, scientific journal manuscripts and abstracts for publication.
Should conduct comprehensive literature searches to enhance background understanding, and evaluate and analyze the information.
Support in medical affairs activities related to Himalaya products. Provide support to marketing team for responding scientifically to the medical queries raised by the Doctors/ Field staff.
CLick & apply here:-
http://careers.himalayawellness.com/job ... 04275?xp=1