Clinical Trial Manager (Biopharmaceutical, Hellerup)

Job summary

Seeking a Clinical Trial Manager to oversee global clinical trials in a biopharmaceutical setting, focusing on endocrine rare disease programs. The role involves operational management and collaboration with cross-functional teams to ensure trials are conducted effectively and efficiently.

Qualifications

• Relevant academic degree (bachelor’s or master’s) in natural or health sciences (biology, pharmacology, pharmaceutical science or equivalent).
• Minimum of two years of experience in managing clinical trials.
• Proficient in English, both written and spoken.

Responsibilities

• Set up trials operationally, including vendor selection and management, and contribute to operational management plans.
• Develop patient information/consent forms, data collection forms, and trial-specific manuals.
• Participate in the identification, qualification, initiation, and close-out of clinical trial sites.
• Communicate with trial site staff to foster relationships and engagement.
• Oversee and ensure quality control of the Trial Master File (TMF).

Skills

Travel

• Strong understanding of GCP and relevant regulatory guidelines.
• Analytical and structured problem-solver with a proactive approach.
• Ability to balance detail orientation with progress.
• Strong team player with an entrepreneurial mindset.
• 10-20 days per year.