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SoluStaff is recruiting on behalf of our client a specialty pharmaceutical company who is seeking a Medical Affairs Director with expertise in Cardiovascular. The successful candidate will be responsible for providing medical and scientific leadership to support product development, new product launch and post-launch activities. The ideal candidate will be knowledgeable of the regulatory environment, have a strong understanding of clinical trial design and execution, be an expert in cardiovascular medicine, and be able to effectively communicate complex information to both internal and external stakeholders.

Responsibilities

• Deliver Cardiovascular medical and scientific expertise to support product development, launch, and post-launch activities
• Lead advocacy and development of key opinion leaders, academic institutions, and medical societies
• Build and execute scientific platform, disease awareness programs, messaging and training for internal and external audiences
• Collaborate with internal cross-functional teams to develop clinical strategies, execute clinical trials, and product launch planning and execution
• Develop and maintain medical and scientific communications with internal stakeholders, KOLs, and external stakeholders
• Provide medical input for regulatory submissions and commercial asset messaging
• Manage Investigator Initiated Research requests
• Monitor and analyze the scientific literature and competitive landscapes to support business decisions
• Establish and maintain the scientific integrity of all medical information generated by the organization
• Participate with leadership team to ensure alignment and drive product adoption and performance

Requirements

• PharmD, MD or PhD in a relevant field
• 10+ years of experience in medical affairs/medical science liaison in pharmaceuticals
• Cardiovascular and/or Surgery Therapeutic area expertise preferred
• Knowledgeable of regulatory requirements and clinical trial design and execution
• Hands-on experience in developing and executing clinical trial protocols
• Experienced with KOL management, advocacy and scientific society engagement
• Excellent verbal and written communication skills, with the ability to effectively communicate complex information to both technical and non-technical audiences
• Leadership skills with strong interpersonal and relationship-building skills, the ability to collaborate cross-functionally, and work effectively in a team environment.
• Live in the greater Philadelphia region preferable, or near a major airport hub

Benefits

• Annual Bonus based on KPIs
• Paid Time Off
• Medical, Dental, Vision and other Voluntary benefits
• Paid Parental Leave
• Tuition Assistance
• Discretionary Bonus Plan
• Competitive 401(k)