Responsible to work on Protocol development, Clinical study reports, and Investigator's brochure, Clinical Evidence Summaries, Risk-benefit analysis reports.
To perform tasks including literature search, summarizing and analyzing data from clinical studies, consulting, editing statistical and clinical reports
Review of medical journals and technical reports
Review Protocols, CRF`s, ICF`s and miscellaneous study documentation
Working closely with doctors, researchers and other medical services personnel to provide information which is accurate and easy for others to understand
Development of disease specific monographs
Provide protocol related clinical and scientific information to team members and investigators
Serve as primary sponsor contact for the assigned project medical writing activities
Interact with other functional units, such as project management, data management and statistics to ensure client satisfaction through successful execution and completion of projects on time and within budget
Attributes: Self-motivated and motivational, self-starter, positive team player, adaptable, willing to travel up to 10% of the time.