Job Description

POSITION: Medical Affairs Manager

WHERE: Remote

DURATION: 12 - months with possible extension

INTERVIEWS: 2 Rounds 30 minutes virtual - 1:00PM /2:00PM Friday

START DATE: ASAP

Pay Rate: $95/HR-$120/HR (flexible)

Must Haves:

• 9 years of total experience working in a similar role/environment
• Minimum 3 years of that experience must be in Interventional procedures/ injectors (cardiovascular or radiology space)
• Minimum of 6 years of that experience must be in Medical Affairs. This includes but is not limited to:
• Evidence generation, planning and execution – focused on supporting marketing claims/materials, not for clinical trials/pharma
• Investigation initiated research
• Advisory board activities including creating training materials
• Working experience planning and conducting of scientific advisory boards with key opinion leaders
• Extensive medical devices experience and medical device lifecycle knowledge with a focus on cardiovascular and radiology equipment

Summary:

Our client is seeking a dynamic and detail-oriented Medical Affairs Professional to join the team. This role will focus on assisting in the strategic planning and execution of bench, pre-clinical evidence studies, facilitating scientific advisory boards, and developing training materials for life cycle and new product development products. The ideal candidate will have a strong background in medical affairs, excellent communication skills, and a commitment to advancing medical knowledge and product understanding.

Key Responsibilities:

Evidence Studies Planning and Execution:

• Assist in the strategic planning and execution of bench, pre-clinical, and clinical evidence studies to meet regulatory requirements regarding clinical performance and marketing evidence for substantiating marketing claims.
• Collaborate with cross-functional teams to ensure study designs, methodologies, and timelines align with organizational objectives and regulatory guidelines.

Scientific Advisory Boards:

• Assist in the planning and conducting of scientific advisory boards with key opinion leaders (KOLs) to gather insights and feedback on clinical strategies and product development.
• Utilize advisory boards to inform product positioning and marketing strategies and prepare meeting materials, discussion guides, and presentations.

Training Material Development:

• Assist in the development of training materials for life cycle products, ensuring content is scientifically accurate and aligned with product messaging and regulatory requirements.
• Support the planning and development of training materials for internal and external customers related to new product development projects.
• Collaborate with subject matter experts to create comprehensive training resources that address the needs of both internal teams and external customers.
• Articulate material from the evidence library to support the education of medical colleagues across all regions supporting the creation of medical 2-pagers.

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