Medical Director/Senior Medical Director, Medical Affairs (Remote)

Posted 8 months agoViewed
United StatesFull-TimeBiotech
Company:
Location:United States, EST, Central
Languages:English
Seniority level:Director, 5-10 years
Experience:5-10 years
Skills:
LeadershipProject ManagementCross-functional Team LeadershipProduct DevelopmentStrategyCommunication SkillsAnalytical SkillsCollaborationComplianceRelationship buildingProblem-solving skillsResearch
Requirements:
MD required 5-10 years of experience in medical affairs within the pharmaceutical or biotech industry Prior experience in developing medical strategic and tactical plans for drug launch is highly preferred Deep understanding of clinical development, regulatory landscape, and scientific communications Hands-on, roll-up-your-sleeves attitude Collaborative, solutions-oriented Excellent communication skills Relationship building capabilities Proven ability to influence decision-making without authority Willing and able to travel and regularly meet with HCPs/KOLs Proven track record in leading medical strategy and supporting clinical development Strong analytical and problem-solving skills Demonstrated ability to interact with senior management, academic experts, and patient advocates
Responsibilities:
Develop and execute the medical affairs plan aligned with product lifecycle stages. Support publications, abstracts, posters, and medical slide decks. Collaborate with Preclinical, Clinical Development, and Regulatory teams. Provide medical leadership in relevant therapeutic and disease area initiatives. Interact with investigators, KOLs, and research institutions. Support short and long-term goals of Medical Affairs regarding research interests and collaborations. Ensure alignment of Medical Affairs activities with launch readiness and program management plans. Provide medical review and approval of external resources and publications. Assist with planning and execution of advisory boards. Ensure all medical activities adhere to legal, regulatory, and corporate compliance standards. Represent company at scientific and clinical congress meetings. Develop and deliver medical education and training materials. Lead efforts of developing patient registries and disease awareness campaigns.
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