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Senior Clinical Research Associate, Contractor, Denmark

3+ years
DKK 600,000 – 750,000 annually
10 July 29, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Senior Clinical Research Associate, Contractor
Location: Denmark
Job Type: Contract | Category: Clinical Operations
Estimated Salary: DKK 600,000 – 750,000 annually (based on Danish clinical contractor benchmarks)


About Biorasi:
Biorasi is a full-service, award-winning Clinical Research Organization (CRO) built on innovation, flexibility, and a deep commitment to delivering excellence. We empower our team to grow professionally while enabling the advancement of life-changing therapies worldwide.


Role Summary:
As a Senior Clinical Research Associate (CRA) Contractor based in Denmark, you’ll oversee all aspects of site monitoring activities to ensure clinical trial quality, integrity, and adherence to international regulatory standards. This remote role includes significant site-facing responsibilities with travel as required.


Core Responsibilities:

  • Conduct all required site visits: selection, initiation, monitoring, and close-out

  • Prepare visit reports and follow-up letters post-site visits

  • Manage study progress: ethics approvals, subject recruitment, data entry, query resolutions

  • Coordinate logistics of investigational products, supplies, and study documents

  • Attend Investigator Meetings and contribute to protocol and training delivery

  • Review documents for GCP compliance, protocol adherence, and safety monitoring

  • Collect and manage essential documents in eTMF

  • Train and support site personnel on study protocols and expectations

  • Evaluate site performance and ensure regulatory compliance

  • Participate in audits and implement corrective actions

  • Provide feedback and oversight on CRA/CTA performance and resource allocation

  • Mentor junior team members and participate in regular team meetings


Candidate Profile:

  • Bachelor’s degree in biomedical sciences or related discipline

  • Fluent in English and the local Danish language

  • Minimum 3 years of CRA experience (monitoring or coordinating)

  • Proficiency in ICH-GCP and global regulatory standards

  • Excellent verbal and written communication skills

  • Familiarity with Microsoft Office (Word, Excel, PowerPoint)

  • Willingness to travel up to 70% as needed

  • Strong planning, time management, and problem-solving skills


Why Join Biorasi?

  • Work with a globally recognized CRO

  • Be part of a collaborative, fast-moving, and supportive team

  • Gain exposure to diverse therapeutic areas and study models

  • Contribute directly to improving global health outcomes


How to Apply:
Submit your application via
biorasi.com or email your CV to careers@biorasi.com