Work mode: Hybrid

Onsite Location(s):Madrid, M, ES

• Develop and execute a comprehensive clinical affairs strategy for the EMEA region that aligns with the organization's global objectives.

• Lead and mentor a team responsible for professional education programs, ensuring high-quality training and development opportunities for healthcare professionals.

• Oversee the planning and execution of ISRs and collaborative trials, ensuring compliance with regulatory standards and ethical guidelines.

• Foster strong relationships with EMEA RM leadership, divisional clinical leadership, and key stakeholders to facilitate collaboration and support cross-functional initiatives.

• Drive the creation and dissemination of clinical evidence to support product positioning and market access strategies.

• Monitor and analyze industry trends, clinical data, and competitive landscape to inform strategic decisions and identify opportunities for growth.

• Ensure adherence to Good Clinical Practice (GCP) and other relevant guidelines to maintain the highest standards of clinical research integrity and patient safety.
  
  

• Advanced degree in a relevant scientific or medical field.

• Extensive experience in clinical affairs, preferably within the medical device or pharmaceutical industry, or experience of directing research within an academic environment.

• Demonstrated leadership in building and managing professional education programs and clinical trials.

• Strong understanding of the regulatory environment and GCP guidelines in the EMEA region.

• Excellent communication, negotiation, and interpersonal skills, with the ability to engage effectively with diverse teams and stakeholders.

• Fluent in English, with proficiency in additional EMEA languages being an advantage.