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Experienced Clinical Research Associate (Home-Based, Anywhere In Denmark

1-2 years
Not Disclosed
10 Dec. 6, 2024
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ 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 Denmark)
Location: Copenhagen, Denmark (Home-Based)
Job ID: 9303

Job Summary:
Medpace is rapidly expanding and seeking full-time, home-based Clinical Research Associates (CRAs) to join our Clinical Operations team in Denmark. This role offers the opportunity to be part of a Nordic team, contributing to the success of various projects and tasks in the drug development process. If you are passionate about clinical trials and want to advance your career while working remotely, this is a great opportunity for you.

As a Clinical Research Associate at Medpace, you will be involved in every stage of the drug development process, supporting customers and ensuring successful clinical trials. This position is ideal for those with a medical or healthcare background who are interested in traveling and playing a crucial role in clinical research.

Responsibilities:

  • Conduct feasibility, pre-study, initiation, monitoring, and closeout visits for research sites, primarily for phase 1-3 trials across various therapeutic areas.
  • Perform source document verification and case report form reviews.
  • Review regulatory documents.
  • Manage study drug inventory.
  • Report and follow up on adverse events and serious adverse events.
  • Assist with patient recruitment and retention.

Qualifications:

  • Bachelor of Science in a health-related field.
  • At least 1.5 years of independent CRA monitoring experience.
  • Strong knowledge of medical terminology and clinical patient management.
  • Basic knowledge of drug therapy techniques and clinical research methodologies.
  • Fluency in the local language and excellent English 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. Our mission is to accelerate the global development of safe and effective medical therapeutics.

Why Medpace?

  • Flexible work environment
  • Competitive compensation and benefits
  • Competitive PTO packages
  • Structured career paths with professional growth opportunities
  • Company-sponsored employee appreciation events
  • Employee health and wellness initiatives
  • Recognized by Forbes as one of America's Most Successful Midsize Companies (2021-2024)

Join Medpace today and be part of a company that makes a difference in global healthcare.