Initiating, performing robust project plans, and delivering it within the stipulated timelines.Developing strategies to promote the brand in the competitive market by providing scientific content and patient education input.Conceptualizing and/or developing high quality patient education inputs.Project management (assigning projects to the juniors and training new joiners). Performing peer review and proof-reading (but not limited to quality check) of the articles written by senior and junior writers/editors.Final proof reading and quality check of the designed inputs.

Initiating, performing robust project plans, and delivering it within the stipulated timelines.Developing strategies to promote the brand in the competitive market by providing high quality scientific content and patient education input.Conceptualizing and/or developing high quality patient education inputs.Project management (assigning projects to the juniors and mentoring new joiners). Performing peer review and proof-reading (but not limited to quality check) of the articles written by senior and junior writers/editors.Final proof reading and quality check of the designed inputs

Developing/writing high quality scientific content for CME, drug monographs, brochures, newsletter, detail aids, journals, health magazines, patient information leaflets, review articles, journal updates, newsletters and conference updates for print and electronic mediaWriting review articles and case studies

Providing content approach for the projectsDeveloping scientific content and patient education materialPerforming peer review and proof-reading of the articles

• Developing scientific content for product monograph, handbooks, health magazines, information leaflets, print materials and content for electronic media. • Developing algorithms by compiling scientific data (information pertaining to diagnosis and/or treatment/ management) from various international guidelines. • Developing case studies.• Assisting Senior writers/ Managers in searching articles for development of TOC (Table of Content) for different scientific inputs.

Enrollment of patient after thorough screening (evaluation of inclusion and exclusion criteria) Collection and interpretation of laboratory reportsSpontaneous reporting of adverse drug reactions (ADRs)Detection and evaluation of ADRs.Documentation of ADRs in Pharmacovigilance form provided by CDSCO (Central Drugs Standard Control Organization)