Sr. Clinical, Medical & Regulatory (CMR) Director

International pharmaceutical company is looking for Sr. Clinical, Medical, Regulatory (CMR) Director.

You will be responsible for the execution of registration, clinical trials, medical affairs, corporate travel and event in full compliance with local procedures, corporate and legal requirements. The job requires a patient-centric mindset and strong business knowledge to be able to drive the department.

The position requires strong medical knowledge and expertise, and the person is perceived by the local market as a respected medical professional. The role requires seniority experience in both, technical expertise knowledge as well strong leadership skills.

As a CMR Director in a senior management leadership role, you will get the opportunity to join and lead a department of 30+ employees. You will report directly to the affiliate General Manager, and you will also be a part of the Leadership Team.

Key responsibilities:

• Leading and developing CMR team;
• Contributing actively to decisions as a member of the leadership team;
• Driving operational excellence in Medical, Regulatory Affairs, Clinical Trials, Corporate travel and event functions;
• Providing scientific insights and support with the relevant stakeholders;
• Identifying, contacting, developing, and maintaining relations with key opinion leaders, key scientific medical institutions and other Health Care Professionals (HCPs) to make the company a valuable partner in providing better care for patients;
• Ensuring compliance of medical activities, educational materials with the legislation and company requirements;
• Ensuring planning and execution of medical activities to support business in general;
• Directing maintenance of existing product approvals and decisions of filing of new product approval applications (when applicable);
• Ensuring PV process development and maintenance;
• Leading corporate travel and event function, ensuring well established business processes;
• Ensuring representation of CMR function at the regional level.

Qualifications:

• You have a Doctor of Medicine degree with at least 15+ years of experience in the international pharmaceutical industry;
• 7+ years of managerial experience including managing Head of departments;
• Experience in engaging with regulatory bodies and industry KOLs, able to influence and build strong and trusted relationships;
• Excellent leadership and people development skills;
• English from Advanced level;
• Excellent written and verbal communication skills, including communication across functions and strong presentation skills;
• Management and coaching skills;
• Strategic mindset.