BIOSPHERE CLINICAL RESEARCH PVT LTD & Sprutha Impex Pvt Ltd

To write, review, and edit scientific medical writing. Prepare clinical study reports, study protocols, annual reports, Investigator’s Brochure. Review of study protocols, CRF, ICF, subject questionnaire and its compliance with regulatory bodies. Cross checking of IEC summary reports, Investigator’s Brochure…

Monitors the progress of the clinical activities in the assigned studies in accordance with Protocol, SOPs, applicable Regulatory & ICH/GCP guidelines and implements actions as necessary. Plans and manages the project timelines and resources. Participates in project meetings, provides regular…