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 phramacology 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
• Work with multinational project teams and coordinate activities on multiple projects
• Interact effectively with clients
• Keep abreast of professional information and technology through literature, symposia, and conferences
• Function independently with initiative and minimal guidance
• Have attention to detail and focus on quality
• Have excellent English writing skills, strong verbal and written communication skills
• Work effectively in a team setting, take over additional responsibilities
• Contribute to cross-functional working groups as needed.