Virendra P. S. Rathor's Linkedin Analytics

• More than 13 years of work experience in the field of clinical research, scientific/ medical writing, and pharma product development. • Responsible to produce abstracts, short communications, manuscripts, review articles, manuscript slide sets (PDF, MS-Power Point & Word), slide sets for posters, and, oral presentations at scientific congresses. • Responsible for the planning, writing, editing, reviewing, and coordinating of the publication of clinical data in pein-reviewed journals as per agreed timelines and quality. • Working together with key client counterparts at clients' locations to facilitate the completion of project ct and their appendices. Understanding new agreements and changes due to SOPs and regulatory guidelines. • Trained in writing regulatory documents such as clinical study reports, investigator brochures, protocols, and informed consent forms according to the ICH-GCP guidelines. • Expertise in drafting and presenting clinical and scientific data, scientific presentations, research proposals, progress reports and research results to colleagues and other professionals in accordance with all applicable guidelines. • Experience in facilitating/mentoring subordinates by using interactive discussions & “hands-on” approaches to help subordinates learn & attain proficiency in subjects. • Sound knowledge of different regulatory guidelines as applicable