trial

Genmab in Copenhagen seeks a Senior Clinical Trial Manager (CTM) to drive the success of our global clinical studies with strategic oversight and cross-functional collaboration. You will partner with Clinical Trial Teams, CROs, and investigators to ensure studies are executed on time, within budget, and in full regulatory compliance.With 8+ years in clinical...

Key Responsibilities Support the planning, setup, and execution of global clinical trials, ensuring activities are delivered in accordance with timelines, quality standards, and regulatory requirements. Ensure trial oversight by maintaining accurate documentation and participating in inspection readiness activities. Collaborate with CROs and internal...

At Genmab, we are dedicated to building extra[not]ordinary® futures, together, by developing antibody products and groundbreaking, knock-your-socks-off KYSO antibody medicines® that change lives and the future of cancer treatment and serious diseases. We strive to create, champion and maintain a global workplace where individuals’ unique contributions...

At Genmab, we are dedicated to building extra[not]ordinary® futures, together, by developing antibody products and groundbreaking, knock-your-socks-off KYSO antibody medicines® that change lives and the future of cancer treatment and serious diseases. We strive to create, champion and maintain a global workplace where individuals’ unique contributions...

Gan & Lee Pharmaceuticals seeks a Clinical Operations Professional to work closely with the Clinical Operations Team on day-to-day management of clinical studies. The role will be based in Denmark or the United States, reporting to the Head of Clinical Operations.You will help ensure quality and regulatory compliance, maintain study materials, and support...

SummaryThis position reports to the Head of Clinical Operations, Gan & Lee Pharmaceuticals USA Corporation or designee. This role is responsible for working side-by-side with the Clinical Operations Team, assisting with day-to-day management of clinical studies. The position will be based in either Denmark or US.Education and CredentialsCollege degree in...

Job SummaryOur clinical activities are growing rapidly, and we are currently seeking a full-time Clinical Trial Site Relationship Coordinator to join our vibrant Clinical Operations team in Denmark, Copenhagen. This is a fantastic opportunity to work on pre-award and post-award study feasibilities, build and maintain strategic relationships with our network...

Rigshospitalet søger en energisk og involverende CTU-sygeplejerske til at være medansvarlig for afdelingens trials og bidrage til forskning og udvikling. Du vil arbejde tæt sammen med et tværfagligt personale og patienter for at sikre optimale forløb og avanceret behandling.Stillingen kræver autorisation som sygeplejerske, GCP-kursus og erfaring med...

Medpace, Inc. in Copenhagen, Denmark is seeking a full-time Clinical Trial Site Relationship Coordinator to support site relationships and feasibility activities across Denmark and Finland.You will help with pre- and post-award study feasibilities, site selection, and study start-up while developing strategic plans for site engagement. The role requires...

Medpace Overview Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through the advancement of clinical...

    Do you enjoy advising senior leaders and turning complex information into strategic recommendations? Join us to strengthen how one of the world’s largest clinical development organisations plans resources, monitors performance and delivers its global clinical trial portfolio.   Your new role As Senior Manager in Trial Resource & Performance...

Novo Nordisk in Denmark is seeking a Trial Resource and Performance Senior Manager to support strategic resource planning, capacity management, and portfolio prioritization across global trials. You will translate complex data into actionable recommendations for Global Trial Portfolio leadership and key executives.You will partner with leadership to drive...

Genmab seeks a Contract Manager to lead end-to-end management of Clinical Trial Agreements (CTAs) and FMV negotiations. You will serve as the primary contract execution contact, ensuring compliance and maintaining inspection-ready records across sites. Strong negotiation and cross-functional collaboration are essential. The role requires experience in...

Novo Nordisk is seeking a Senior Manager for Trial Resource & Performance Management to translate complex data into clear recommendations for Global Trial Portfolio leadership. You will influence resource planning, capacity management and portfolio priorities, collaborating across Clinical Operations, Trial Operations and Clinical Data Management to drive...

Your new role As Senior Manager in Trial Resource & Performance Management, you will work at the intersection of strategy, operations and analytics. Acting as a trusted advisor to Global Trial Portfolio leadership, you will translate complex data into clear recommendations and help leaders make informed decisions about resources, capacity and portfolio...

Genmab is seeking a Senior Manager, Inspection Readiness to strengthen Clinical Trial Operations and ensure GCP compliance across trials and external providers. You will drive process improvements, deliver training, and lead readiness activities in a global environment. The role requires leadership in quality events and ongoing risk mitigation, with a focus...

We are extra[not]ordinary*(ex· tra· not· or· di· nary |\ ik-ˈstr-not-ȯr-də-ˌner-ē)Adjective: A unique word for Genmab meaning to go way beyond what isusual; to be remarkable; proudly unique and authenticBack to search resultsPrevious job Next jobJOB DESCRIPTIONAt Genmab, we are dedicated to building extra[not]ordinary® futures, together, by...

The Copenhagen Trial Unit (CTU) invites applications for a time-limited, full-time PhD fellowship starting 1 October 2026. The PhD project focuses on assessing and reporting environmental impacts in clinical trials and contributing to SPIRIT-ICE and CONSORT-ICE guidelines in collaboration with an international group.The successful candidate will perform...

Novo Nordisk A/S is seeking a Senior Clinical Data Scientist to lead data science activities across global development programmes. You will collaborate with trial teams, regulatory experts, and external partners to ensure high-quality, submission-ready data and documentation. The role includes input on trial design, SDTM/ADaM and TFL deliverables, and...

Novo Nordisk A/S is seeking a Senior Clinical Data Scientist to lead data science activities across global development programmes. You will collaborate with trial teams, regulatory experts, and external partners to ensure high-quality, submission-ready data and documentation. The role includes input on trial design, SDTM/ADaM and TFL deliverables, and...