Associate Medical Director (Clinical Development, Biopharmaceutical, Hellerup)

Job summary

This role involves leading drug development initiatives for rare conditions, focusing on clinical trial design and regulatory interactions. The position is based in Hellerup and requires collaboration with global teams to ensure the success of clinical programs.

Qualifications

• M.D. degree, preferably with a Ph.D.
• 5-7 years of relevant industry experience, with consideration for post-graduate clinical or academic experience.
• Strong background in scientific and clinical inquiry.
• Excellent written and oral communication skills.
• Sound judgment in handling complex and confidential information.

Responsibilities

• Formulate and implement Clinical Development Plans.
• Design and oversee clinical trials, ensuring site and subject retention.
• Serve as Medical Monitor, ensuring study integrity and tracking safety and efficacy data.
• Lead teams of medical monitors and study teams.
• Complete trial-related documents in collaboration with cross-functional teams.
• Analyze and report clinical data, contributing to regulatory strategies and submissions.
• Maintain knowledge of relevant science and regulatory guidance.
• Collaborate with cross-functional colleagues to optimize product development.
• Cultivate relationships with investigative sites and key opinion leaders.

Skills

• Ability to learn quickly in fast-paced environments.
• Strong ownership and leadership qualities.
• Effective collaboration across organizational levels.
• Proficient in managing complex instructions and multiple priorities.

Education

• M.D. degree required; Ph.D. preferred.

Tools

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