Responsibilities:

· Prepare and provide functional area inputs in preparation of pharmacology sections of clinical and non-clinical documents

· Aid in preparation of documents such as registration dossiers, responses to health authorities in addition to documents such as nonclinical and clinical overviews and summaries, etc.

· Be accountable for quality and adherence to timelines at different stages of all projects

· Perform detailed literature search utilizing both public and private databases and show apt while synthesizing the results

· Coordinate with medical writers (and other cross-functional teams) in the data review, analysis and reporting of pharmacology studies.

· Be responsible, in conjunction with medical writer, for overall content and accuracy of study report before forwarding for final sign-off. Assist with internal and external dissemination of results to Development Team, Investigators etc.

· Provide mentoring, and training for other team members