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Medical Director, Wound Reconstruction and Care, Medical Affairs
3 months ago
Changing lives. Building Careers.
Joining us is a chance for you to do important work that creates change and shapes the future of healthcare. Thinking differently is what we do best. To us, change equals opportunity. Every day, more than 4,000 of us are challenging what’s possible and making headway to help improve outcomes.
Reporting to the Sr. Director, Global Medical Affairs, Wound Reconstruction and Care, we are seeking a highly motivated and experienced
Medical Director, Wound Reconstruction and Care (WRC)
to join our Medical Affairs team. The incumbent will be a strategic, hands-on clinical expert playing a crucial role in shaping and executing the medical affairs strategy to support the company’s objectives and ensure the appropriate dissemination of medical information to various stakeholders. He/she will be involved in data gap analysis and planning and executing evidence generation, including company sponsored studies, collaboration projects, and investigator-initiated studies (IIS), potentially serving as study director and medical monitor.
Essential Duties and Responsibilities:
Provide support for planning and execution of the WRC medical affairs strategy, aligning with the company’s goals and objectives including strategic plans for key opinion leaders engagement, insight gathering, evidence generation, data dissemination, publications, and congresses
Maintain deep knowledge of disease areas as well as an understanding of patient and surgeon interactions, clinical decision making and impact.
Serve as study director for trials: provide critical medical input into the lifecycle management strategies in responsible therapeutic areas.
Serve as medical expert providing direction for assigned products and therapeutic areas, scientific communications, publication planning/review, advisory boards, health outcome plans, MSL activities, speaker programs, Investigator-Initiated-studies (IIS), and CME grant reviews or other internal key business processes.
Responsible for approval of medical and scientific content of Regulatory, Safety, Medical Affairs, and Commercial inputs for assigned therapeutic areas.
Attend national and regional medical meetings and symposia and engage in discussions with attendees as appropriate; attend scientific sessions and poster presentations, gather information, and summarize findings
Prepare and deliver fair-balanced and objective clinical and scientific presentations on company products to HCPs, payors, and patient organizations and participate in panel discussions as needed
Build and maintain professional relationships with healthcare professionals (HCPs), thought leaders, medical groups, academic institutions, and national/regional professional societies
Provide clinical and scientific support for HCPs, including answering unsolicited medical inquiries about Integra’s products and other related issues
Identify and train speakers for advisory boards, symposia, and educational programs with company-approved materials, slide sets, abstracts, posters, etc.
Participate or lead as needed the review and assessment of new business opportunities
Desired Qualifications:
M.D. degree required
Prior (5+ years) medical affairs experience in a pharmaceutical or MedTech company is preferred
Proven track record of developing and executing medical affairs strategies to support product development, launch, and lifecycle management
Previous participation in a clinical development program is essential, including involvement in all stages of clinical trials (i.e. from start up to study report), ideally having taken at least one program through to a licensing application.
Experience in field strategy and execution in Burns and/or Plastic and Reconstructive Surgery is preferred.
Excellent communication and presentation skills, with the ability to effectively communicate complex scientific and medical information to diverse audiences.
Willingness to learn new therapeutic areas and technologies
Demonstrated ability to execute and deliver results in a deadline-driven environment while managing multiple priorities
Strong team orientation and passion for continuous self-development
WORKING CONDITIONS
US based
Remote
Travel: 25-35%
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