Senior Medical Director (Rheumatology, EMEA, Office-based)

Job summary

This role involves providing strategic leadership and oversight for the clinical and medical aspects of drug development in rheumatology. The position requires the design and execution of Clinical Development Plans and protocols, ensuring compliance with GCP regulations while improving health outcomes through effective clinical trials.

Qualifications

• MD degree with at least 5 years of experience in clinical drug development, specifically in rheumatology.

Responsibilities

• Lead the medical content and oversight of clinical studies.
• Act as the therapeutic lead and ensure subject safety throughout trials.
• Regularly review clinical data and collaborate with safety committees.
• Approve and contribute to clinical documents such as protocols and reports.
• Recruit and guide clinical investigators, ensuring compliance with SOPs and GCPs.
• Participate in long-range strategic planning and provide line management.

Skills

• Strong problem-solving abilities and leadership skills.
• Expertise in clinical trial design and regulatory submissions.
• Excellent written and verbal communication skills.
• Willingness to travel as required.

Education

• MD degree with a minimum of 5 years of clinical drug development experience.

Tools

• Familiarity with clinical trial management systems and regulatory documentation processes.