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Gan & Lee Pharmaceuticals in Denmark invites an experienced Senior Clinical Trial Manager to lead end-to-end sponsored trials, from protocol feasibility to submission, ensuring compliance with GCP, ICH, and company procedures.You will oversee CROs, TMFs, budgets, recruitment plans, and study timelines, collaborating with cross-functional teams to deliver...

Pharmacosmos A/S is seeking a Director of Drug Safety Operations to combine leadership with operational excellence in a global safety function. You will oversee safety operations, lead seven Drug Safety Associates, and report to the VP Global Drug Safety, guiding AI-driven process improvements.The role requires a life sciences degree and proven...

Fortrea is seeking a Clinical Research Associate (CRA) for on-site monitoring, focusing on site management and compliance with ICH GCP. The role requires at least two years of clinical monitoring experience and a degree in life sciences or a related field.The CRA will conduct PSV, SIV, and routine visits, ensure patient safety through informed consent...

Zealand Pharma A/S is seeking a regulatory/compliance professional to lead inspection readiness activities and support regulatory inspections. You will develop and manage processes, provide GCP guidance, and ensure compliant record management across the organization.The role requires a Life Sciences degree, strong knowledge of ICH-GCP/FDA/EMA, and experience...

Genmab in Copenhagen is seeking an experienced Clinical Trial Manager to support the planning and execution of global clinical trials. The ideal candidate will have over 5 years experience in clinical trial management and a strong understanding of ICH/GCP regulations.The role involves collaborating with CROs and internal stakeholders to ensure trials meet...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionJoin Us as a Senior Clinical Research Associate (Level I) – Make an Impact at the Forefront of InnovationWe have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years.As part...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionJoin Us as a Clinical Research Associate (Level II) – Make an Impact at the Forefront of InnovationWe have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years.As part of our...

Join Fortrea as a CRA – exciting future opportunities for a single sponsorWe’re excited to invite CRAs to join Fortrea, where you’ll work with one dedicated sponsor.Key RequirementMinimum 2 years of clinical monitoring experiencePreferably 1+ year experience in oncology studiesSummary Of ResponsibilitiesManage clinical trial sites in line with Fortrea...

Operational Strategy & Clinical DevelopmentContribute to the development of operational strategies and clinical development plans for ongoing and future programsSupport study planning activities, including timelines, resource forecasting, operational feasibility assessments, and budget estimatesProvide guidance on CRO, vendor, and site selection strategies...

Emerald Clinical Trials is expanding its European operations and building a pipeline of experienced Clinical Project Managers to support upcoming studies. This home-based role offers the opportunity to lead global and regional trials across renal, oncology, cardiometabolic and autoimmune diseases.We seek candidates with 7+ years in clinical research and at...

Zealand Pharma A/S is seeking a regulatory-focused professional to lead inspection readiness for clinical trials and provide GCP advice across teams. You will develop and manage SOPs, checklists, and guides while supporting regulatory inspections and audits.The ideal candidate brings a Life Sciences degree with biotech/pharma experience, deep ICH-GCP...

Hemab Therapeutics seeks a Senior CTM to lead end-to-end clinical trial management across Europe. You will oversee CROs, sites, and vendors, ensure ICH/GCP compliance, and coordinate trial start-up and regulatory submissions. The role requires global study oversight, strong communication, and travel 20–30%.Based in Europe, you will partner with...

Provide scientific and GMP expertise to Contract Manufacturing Organisations (CMOs) and other stakeholdersEnsure robust and efficient analytical programs are implemented at CMOs and maintained throughout the product life cycleLead analytical activities, including submissions, from post-phase 3 clinical studies through the commercial life cycleLead regulatory...

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...

Join Fortrea as a CRA – exciting future opportunities for a single sponsorWe’re excited to invite CRAs to join Fortrea, where you’ll work with one dedicated sponsor.Key requirement:Minimum 2 years of clinical monitoring experience Experience in oncology studies preferredSummary of ResponsibilitiesManage clinical trial sites in line with Fortrea SOPs,...

TFS HealthScience is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full service-capabilities, resourcing and Functional Service (FSP) solutions.Join Our Team as a Freelance Senior Clinical Research...

Genmab A/S is seeking an Associate Director, Site Contract Management in Copenhagen. This role entails operational leadership of a team, overseeing Clinical Trial Agreements, and ensuring compliance with legal and regulatory standards. The successful candidate will bring at least 10 years of experience in site contracting, along with people management skills...

ALK is seeking a Senior Regulatory Affairs Manager to lead regulatory strategies across International Markets. You will partner with Global Regulatory Leads and various departments to drive registrations, lifecycle management, and commercialization plans for ALK’s pharmaceutical products on a global scale.The role requires strong expertise in global...

Fortrea seeks a Site Budget & Contract Specialist to negotiate and manage site agreements and related contracts for clinical trials. The role collaborates with study teams, legal, and project management to ensure compliant and efficient contract execution.This is a full-time, permanent, home-based position with remote/hybrid options. Ideal candidates will...

AGC Biologics in Copenhagen/Søborg is seeking a Senior Downstream Scientist to lead technical excellence in commercial manufacturing. You will own downstream process optimization, drive change control, and contribute to regulatory dossiers while guiding audits and inspections.You bring an MSc or PhD with 6+ years in pharma, hands-on chromatography, UF/DF,...