Medical Affairs Manager Urology & Critical Care EMEA

Job Title: Medical Affairs Manager Urology & Critical Care EMEA

Job Location: Winnersh RG41, UK

Job Location Type: Remote

Job Contract Type: Full-time

Join a global leader in advancing the world of health. At BD, we are committed to improving patient outcomes through innovation and collaboration. We are seeking a Medical Affairs Manager for our Urology & Critical Care (UCC) business in EMEA to provide strategic medical support, drive clinical programs, and foster relationships with Key Opinion Leaders (KOLs) across the region.

We are the makers of possible. BD is one of the largest global medical technology companies in the world. Advancing the world of health™ is our Purpose, and it’s no small feat. It takes the imagination and passion of all of us—from design and engineering to the manufacturing and marketing of our billions of Med Tech products per year—to look at the impossible and find transformative solutions that turn dreams into possibilities.

Why join us? A career at BD means learning and working alongside inspirational leaders and colleagues who are equally passionate and committed to fostering an inclusive, growth-centered, and rewarding culture. You will have the opportunity to help shape the trajectory of BD while leaving a legacy at the same time.

To find purpose in the possibilities, we need people who can see the bigger picture, who understand the human story that underpins everything we do. We welcome people with the imagination and drive to help us reinvent the future of health. At BD, you’ll discover a culture in which you can learn, grow and thrive. And find satisfaction in doing your part to make the world a better place.

Become a maker of possible with us! Our vision for BD Interventional at BD: BDI focus on leading innovation and life‑enhancing devices in the field of surgical, endovascular, urological and critical care interventions aiming at advancing the treatment of high burden diseases and enabling surgical and interventional procedures.

As the Medical Affairs Manager, you will play a pivotal role in shaping medical strategy and ensuring alignment with business objectives. You will lead initiatives that support evidence generation, clinical education, and regulatory compliance, while collaborating with cross‑functional teams to deliver impactful solutions for healthcare professionals and patients.

• Medical Review & Compliance:
  Act as Medical Reviewer for Veeva AdProm MLR approval processes, ensuring scientific accuracy and regulatory compliance. Manage Veeva Vault Medical content and analyze feedback from Global Medical Information.
• Training &
  
  Education:
  
  Build and implement training packages for UCC in collaboration with EMEA Marketing and Business Development teams. Support internal projects such as BDLA at the EMEA level.
• Cross‑Functional
  
  Collaboration:
  
  Partner with Public Policy and Market Access teams to integrate medical strategy into broader business initiatives.
• KOL Engagement:
  Lead KOL mapping, development, and engagement planning across EMEA. Ensure compliance with legal and regulatory standards for HCP interactions.
• Evidence Generation:
  Support clinical studies, publication strategies, and dissemination of real‑world evidence. Monitor study progress and manage associated risks.
• Clinical & Technical Support:
  Assist with product evaluations, clinical documentation, and user training activities.
• Project Management:
  Utilize tools such as Pub Med and regulatory databases for data analysis. Track budgets and oversee administrative processes for timely payments.

• Education:
  
  Advanced degree in medicine, nursing, pharmacy, or life sciences (MD, RN, Pharm
  
  D, PhD, MSc preferred).
• Experience:
  
  3–5 years in medical affairs within pharma or medical devices, with global exposure.
• Strong scientific and clinical expertise in Urology, Infection Prevention, and Critical Care.
• Strategic thinker with proven project leadership experience.
• Excellent communication and influencing skills across diverse stakeholders.
• Familiarity with European clinical trial requirements, MDR, and ethical standards.
• Digital fluency with tools…