Senior Clinical Study Manager (Pharmaceutical, Copenhagen)

Job summary

The role involves leading a global trial management team within Clinical Operations, focusing on clinical trials for brain diseases. The position requires collaboration with various stakeholders, including CROs and clinical experts, to ensure effective trial execution and adherence to timelines and budgets.

Qualifications

• MSc degree or higher in medical, pharmaceutical, or biological sciences.
• Over 5 years of experience in clinical trial project management, preferably in the pharmaceutical industry or CRO.
• Experience managing large, late-phase trials across multiple countries.
• Familiarity with rare disorder clinical trials is advantageous but not mandatory.
• Strong communication skills and a multicultural mindset.
• Fluent in English, both written and verbal.

Responsibilities

• Lead and coordinate a cross-functional global trial management team.
• Serve as the primary contact for CROs and vendors, ensuring effective trial execution.
• Oversee vendor management and budget adherence.
• Contribute to process optimization for clinical trials.
• Manage multiple priorities and deadlines through effective communication and problem-solving.

Skills

• Leadership and team management.
• Strong organizational and strategic risk management abilities.
• Customer-focused approach with a proactive work style.

Education

• MSc degree or higher in relevant scientific fields.

Tools

• Experience with clinical trial management systems and project management tools is preferred.