WHO YOU ARE:
Training in medical writing, clinical trial methodologies, research design and ICH – GCP will be added advantage
- Must have working knowledge of Indian regulations pertaining to Health care professionals’ interactions (MCI code of ethics for doctors & UCPMP Code for Pharma) and Drugs and Cosmetic Act regulations pertaining to clinical trials and new drug approvals
· Strong academic record with deep knowledge of the therapeutic area, strength in research with knowledge of research methodologies and interpretation of medical data
· Strategic mindset with scientific acumen and communication skills in order to be accepted by leading specialists in peer-to-peer capacity
- Experience with complex business environments preferred
· Strong track record of success as demonstrated through annual performance ratings and/or professional accomplishments and award
Disclaimer: The preceding job description has been designed to indicate the general nature and level of work performed by employee within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities, and qualifications required of employees as assigned to this job. Nothing herein shall preclude the employer from changing these duties from time to time and assigning comparable duties or other duties commensurate with the experience and background of incumbent(s).
