Sr Spec Medical Affairs

Cordis; Brandon (FL); On-site; USD 120,000 - 180,000; Full time

Job summary

Cordis is seeking a Sr. Medical Affairs Specialist to support cross-regional medical operations and ensure local execution of global strategy.

You will coordinate investigator-initiated studies, manage real-world data, and lead the medical education grant program across regions. You will translate clinical insights into actionable plans, collaborate with quality, regulatory and compliance teams, and align pre- and post-market data strategies with clinical development.

Qualifications

• Bachelor’s degree required; advanced degrees a plus.
• 5+ years in the medtech or pharmaceutical industry, or 3+ years with a Master’s.
• Experience managing complex operations and cross-functional collaboration.

Responsibilities

• Lead IIS coordination and real-world data collection.
• Lead the medical education grant program.
• Support MedInfo process optimization with cross-functional teams.
• Translate scientific and regulatory insights into actionable product lifecycle plans.
• Support post-market activities with quality, regulatory and compliance teams.
• Partner with clinical development to align pre- and post-market data strategy.
• Ensure adherence to SOPs and regional regulations.
• Develop metrics and dashboards to track medical strategy impact.

Skills

Cross-functional collaboration

Organizational skills

Project management

Communication skills

Education

Bachelor's degree in life sciences/medicine/pharmacy/biomedical engineering

Master’s/PharmD/PhD a plus

Tools

Microsoft Office

Job description

Overview

Selution, in partnership with Cordis, specializes in the development of ground-breaking technology and commercialization of advanced drug device combination products for the treatment of coronary and peripheral artery disease. Our mission is to revolutionize healthcare by creating next-generation solutions that address unmet and critical medical needs.

Responsibilities

The Sr. Medical Affairs Specialist will support cross-functional and cross-regional alignment of medical operations and deliverables ensuring strong local execution of global strategy and contributing to operational improvements that enhance internal collaboration, data collection, and compliance.

Key Responsibilities

• Lead handling and processing of ALL investigator-initiated research (IIS) coordination and real-world data collection
• Lead the medical education grant program
• Serve as a key partner with other team members to optimize MedInfo process
• Translate scientific, regulatory, and clinical insights into actionable plans across product lifecycles.
• Support Post market activities in collaboration with key functions such as quality, regulatory, compliance/legal (e.g., risk management, health hazard evaluations, complaint review support registry study data flow, adverse event tracking)
• Partner with clinical development to align pre- and post-market data strategy.
• Partner with Scientific Communications and cross-functional teams to support any requested scientific material development or review
• Ensure adherence to SOPs, ethical guidelines, and regional regulations
• Support leadership in development of desired metrics and dashboards to track impact of medical strategy execution.
• Serve as a subject matter expert in relevant therapeutic areas (e.g., vascular access, interventional cardiology, structural heart), maintaining current and comprehensive knowledge of clinical data, regulatory trends, and competitor positioning
• Collaborate with global and regional stakeholders to optimize Medical Affairs workflows, including processes, systems, platforms and or document management
• Serve as a bridge between global and regional teams including regional medical affairs team mates ensuring alignment on execution and priorities.
• Act as the point of contact for the assigned region for internal stakeholders and identify areas of support in aspects of key product launches, handling off label queries, unsolicited KOL queries and communicate insights to global Medical Affairs leadership. Develop solutions for the same.

Qualifications

• Degree in life sciences, medicine, pharmacy, nursing, or biomedical engineering (Bachelor’s required; Master’s/PharmD/PhD a plus)
• 5+ years of experience in the medtech or pharmaceutical industry or 3+ years of experience w/ a Master’s degree
• Demonstrated ability to manage complex operations and collaborate cross-functionally
• Strong organizational and communication skills
• Proven organizational and project management skills.

Preferred Qualifications

• Experience supporting regional teams (e.g., APAC, EMEA) is preferred
• Excellent communication, leadership, and strategic thinking skills.
• Comfortable in a dynamic, fast-paced, and matrixed environment.
• Attention to detail.
• Proficiency in Microsoft Office.
• Team player with a \"can-do\" attitude.