PRINCIPAL MEDICAL WRITER

Author and review regulatory & other medical writing deliverables independently as per high-quality standards and within expected timelines. Support in building technical & functional expertise within the group by designing & executing robust training programs.

Requirements

• PharmD, M. Pharm, PhD, MD, Post-graduate degree in Life science/medical/para medical
• At least 10- 11 years of experience in medical writing, drug development, clinical research, out of which at least 5 years in core medical writing (regulatory deliverables)
• Proficient with Microsoft Office Suite
• Excellent written and oral communication skills
• Excellent presentation skills
• Strong organizational, problem-solving, and analytical skills
• Ability to manage priorities and workflow
• Versatility, flexibility, and a willingness to work within constantly changing priorities
• Proven ability to handle multiple projects and meet deadlines
• Strong interpersonal skills
• Ability to deal effectively with a diversity of individuals at all organizational levels
• Commitment to excellence and high standards
• Creative, flexible, and innovative team player
• Ability to work independently and as a member of various teams and committees
• Good judgment with the ability to make timely and sound decisions