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Experienced Clinical Research Associate (Home-Based, Anywhere In Norway)

1-2 years
Not Disclosed
10 Sept. 16, 2025
Job Description
Job Type: Full Time Hybrid Remote Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences 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

Experienced Clinical Research Associate (Home-Based, Anywhere in Norway)

Location: Norway (Remote/Home-Based, candidates can be based anywhere in Norway)
Functional Area: Clinical Research Associate
Job ID: 10622
Employment Type: Full-time
Work Arrangement: Home-based


Job Summary:

Medpace is seeking experienced Clinical Research Associates (CRAs) to join our growing team in Norway. This role offers the opportunity to work remotely from anywhere in Norway while supporting Medpace’s clinical trials. Candidates will receive customized, expedited training through the Fast PACE® Training Program for experienced CRAs.

Key Benefits:

  • Retain airline reward miles and hotel reward points

  • Home office furniture allowance, laptop, mobile phone with hotspot

  • In-house travel agents for efficient travel planning

  • Leadership and career advancement opportunities: Lead CRA, CRA Manager, Clinical Trial Manager, Training & Development Manager

  • Fast PACE® training tailored to experience, therapeutic background, and interests

  • User-friendly Clinical Trial Management System (CTMS) with electronic submission of monitoring reports

  • Ongoing therapeutic training by in-house medical and regulatory experts

  • Work with an international team of CRAs

  • Additional perks unmatched by other CROs


Key Responsibilities:

  • Conduct qualification, initiation, monitoring, and closeout visits at research sites in compliance with protocols

  • Communicate effectively with medical site staff, including coordinators and clinical research physicians

  • Verify investigator qualifications, training, and site resources (facilities, laboratories, equipment, staff)

  • Perform source document verification against case report forms; ensure Good Documentation Practices (GDP)

  • Conduct on-site and remote/virtual monitoring using a risk-based monitoring approach, including centralized data review

  • Ensure eligibility of enrolled subjects

  • Review and manage regulatory documents

  • Account for investigational product/drug and medical device inventory

  • Verify and review adverse events (AEs), serious adverse events (SAEs), concomitant medications, and illnesses

  • Assess patient recruitment and retention at clinical sites and suggest improvements

  • Complete monitoring reports and follow-up letters, summarizing findings, deviations, deficiencies, and recommended corrective actions


Qualifications:

  • Minimum 18 months of independent CRA monitoring experience

  • Bachelor’s degree in a health or science-related field

  • Ability to travel 60–70% nationwide within Norway

  • Proficient in Microsoft Office

  • Fluency in local language and excellent English

  • Detail-oriented with strong time-management skills


Medpace Overview:

Medpace is a full-service Clinical Contract Research Organization (CRO) providing Phase I–IV clinical development services to biotechnology, pharmaceutical, and medical device industries. Headquartered in Cincinnati, Ohio, Medpace employs over 5,000 people across 40+ countries. The company leverages local regulatory and therapeutic expertise across oncology, cardiology, metabolic disease, endocrinology, CNS, anti-viral, and anti-infective areas.


Why Medpace:

  • Flexible work environment

  • Competitive compensation and benefits package

  • Paid time off (PTO) and structured career growth opportunities

  • Company-sponsored employee appreciation events

  • Employee health and wellness initiatives

  • Recognized with CRO Leadership Awards from Life Science Leader magazine