Clinical Trial Manager for a 15-month project position at the Clinical Research Unit, Department of Hematology, Rigshospitalet

Would you coordinate national clinical trials and contribute to the development of future treatments for blood diseases to benefit patients?

We seek a structured, independent and engaged academic employee to coordinate sponsor tasks for our newly started strategic initiative: BLOOD-dose.

BLOOD-dose is a national platform trial in hematology, which brings together several clinical trial domains under one shared research and operational structure. The sponsor function is managed by the Clinical Research Unit (KFE) at the Department of Hematology, Rigshospitalet, with a focus on cross-cutting trial coordination, regulatory activities and collaboration between Danish trial sites.

KFE consists of about 35 staff, including trial nurses, bioanalysts, administrative staff and researchers. You will become part of the Sponsorship Office with colleagues who handle coordination of investigator-initiated studies. You will have close collaboration with trial-responsible physicians and nurses and a central role as a link between the participating trial sites and other partners across the country.

Your primary tasks

• Project management and coordination of clinical trials
• Coordination of trial activities across Danish trial sites
• Handling regulatory matters and authority submissions
• Development and handling of collaboration agreements, budgets and protocol changes
• Collaboration with national and international research partners
• Database management and data-legal tasks
• Safety surveillance and management
• Planning and coordination of meetings and preparation of minutes and reporting
• Effective communication between Sponsorship Office, investigators and trial sites

We are looking for you, who

• Have an academic education in health or natural sciences
• Have experience with project management or project coordination, preferably within clinical research
• Work independently, structured and with a strong overview
• Have good IT skills and experience with MS Office
• Master Danish and English in writing and speaking

It is advantageous if you have knowledge of GCP, medical terminology, CTIS and/or REDCap.

We offer

• A central role in a new national research initiative with great strategic importance
• A key function in national and international research projects
• Close collaboration with doctors, study coordinators and research staff
• A dynamic research environment characterized by high professionalism, responsibility and a wide range of tasks
• A flexible workday with a high degree of independence and responsibility
• An informal, engaged and interdisciplinary working environment

Employment: 35 - 37 hours per week in a 15-month project position. Start 1 January 2026 or by agreement.

Additional information

Chief physician, PhD, clinical associate professor Anne Louise Tølbøll Sørensen

Tel. 35 45 18 64 / 40 53 20 12

Application deadline: 2 November 2026

Interviews will be held in week 46 or by agreement.

Salary and terms of employment in accordance with the agreement for academics employed in regions, etc. - agreement 33.01.1.