The JD includes:
Prepares manuscripts, literature review, abstracts, posters, and slide sets working from various data sources including clinical study reports, patient profiles, protocols etc.
Performs quality control (QC) checking / proof reading of literature review, abstracts, posters, and slide sets to meet customer expectations.
Manages up to two assigned team projects at any given time.
Follow and track clinical trial milestones for assigned projects.
Maintain records for all assigned projects including archiving.
Maintain audit, SOP and training compliance.
Performs additional tasks as assigned
The ideal candidate will be a Post Graduate (Except Biology Stream) with 4-5 years of Core Scientific Writing experience in Industry.