Associate Scientific Director/Scientific Director, Dermatology - US Medical Affairs

Responsibilities

• Initiates medical affairs activities, generation and publications and dissemination of data supporting the overall scientific strategy.
• Responsible from Medical Affairs for the design, analysis, interpretation, and reporting of scientific content of protocols, Investigator Brochures, Clinical Study Reports and regulatory submissions and responses.
• Ensures budgets, timelines, compliance requirements are factored into programs' scientific activities.
• Scientific Degree (bachelor's). Advanced Degree PhD, PharmD, PA or NP preferred. Residency or additional post doctorate experience preferred.
• 5-7+ years of experience in the pharmaceutical industry or equivalent; substantial understanding of relevant therapeutic area required.
• Knowledge of clinical trial methodology, regulatory requirements governing clinical trials and experience in the design of protocols preferred.
• May have performed protocol design in the academic environment and/or acted as an assistant PI.
• Interactions normally require the ability to gain cooperation of others, conduct presentations of technical information concerning specifi

Benefits

Additional Information

The Associate Scientific Director/Scientific Director, Dermatology - US Medical Affairs provides specialist medical and scientific strategic and operational input into core medical affairs activities such as: health-care professional and provider interactions; generation of clinical and scientific data (enhancing therapeutic benefit and value); educational initiatives (medical education, scientific communications, and value proposition) and safeguarding patient safety (risk minimization activities and safety surveillance activities). Works closely with sales, marketing, and commercial teams to provide strategic medical input into core brand (product) strategies, and to support medical affairs, marketing activities (promotional material generation and product launches) and market access. Education/Experience Job grade, level, and title will be determined by the selected candidate's credentials, education, and experience. Advanced Degree PhD or PharmD. Additional post doctorate experience highly preferred. 7-10 years of experience in Medical Affairs. Typically, 10-15 years of experience in the pharmaceutical industry or equivalent; substantial understanding of relevant therapeutic area(s) preferred. Minimum of 4 years of clinical trials direct management experience in the pharmaceutical industry or academia or equivalent. 4+ years of experience is preferred. Knowledge of clinical trial methodology, data analysis and interpretation, regulatory requirements governing clinical trials and experience in development strategy and the design of protocols. Ability to support a clinical study independently with little supervision. Proven leadership skills in a cross-functional global team environment. Must possess excellent oral and written English communication skills.

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Company Intel

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