Medical Advisor - Pharma

- Engagement of identified key thought leaders through medical affairs activities, in alignment with the overall strategic plan

- Responsible to ensure optimal execution of strategic medical affairs plan through Regional Medical Affairs including but not limited to medical education, product education, medical evidence generation, advisory boards, pre-license activities and special projects

- A therapeutic area scientific expert, responsible for discussing the scientific data pertaining to products on proactive and reactive basis, patients- treatment trends and studies in the therapeutic areas in which the Company is involved, with defined audience of leading specialists (Physicians, Pharmacists, Hospital Managers, Board Members of Scientific Societies, and other Stakeholders) and to be considered a trusted scientific counterpart

- Responsible for devising optimal training plan to ensure flow of latest medical developments in the given to sales & marketing team

- Jointly responsible with therapy area lead to support optimal patient outcomes through communication of data, information, knowledge and insights in support of healthcare professional needs and organizational goals

- Representing the organization in various internal & external scientific platforms

- Ability to convert insights on disease trends and treatment patterns from key thought leaders into viable and formidable strategic plans to shape the therapeutic areas of interest

- Responsible for identifying knowledge gaps, practice gaps and data gaps and develop strategic medical actions plans including but not limited to medical education, product education, evidence generation and special projects

- Collaborating with thought leaders to conduct therapy specific reviews, meta-analysis, case studies, case series, patient reported outcomes and publish them in journals of repute

RELATED EXPERIENCE REQUIREMENT

- Prefer 2 to 4 years working experience in the pharmaceutical industry or research company in a Medical Advisor capacity

- Experience in the relevant TA preferred

- 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 relationship is essential

- Experience with complex business environments preferred

- Strong track record of success as demonstrated through annual performance ratings and/or professional accomplishments and awards