About the role
Job Title: Experienced Clinical Research Associate, CRA (Home-Based opportunities
Job Location: Remote, Denmark
Job Location Type: Remote
Job Contract Type: Full-time
Job Seniority Level:
Our clinical activities are growing rapidly, and we are currently seeking full-time, home-based Clinical Research Associates to join our Clinical Operations team in Denmark (candidates can be based anywhere in Denmark). This position will work on a Nordic team to accomplish tasks and projects that are instrumental to the company’s success. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you. Fluency in local language and excellent English are required.
If you are looking for a stable, consistently, rapidly, developing CRO, Medpace is a great place for you! We are currently seeking full-time, home or office-based Clinical Research Associates to join our energetic Clinical Monitoring team in the Denmark. We offer an exciting career where you can grow further, using your current and and previous expertise.
Responsibilities
Conduct feasibility, pre-study, initiation, monitoring, and closeout visits for research sites, mainly phase 1 to 3 and within all available therapeutic areas;
Perform source document verification and case report form review;
Perform regulatory document review;
Conduct study drug inventory;
Perform adverse event and serious adverse event reporting and follow-up; and
Assess patient recruitment and retention.
Qualifications
Bachelor of Science in health-related field;
Proven CRA experience of at least 1.5 years independent monitoring experience
Broad knowledge of medical terminology and clinical patient management;
Basic knowledge of drug therapy techniques and clinical research methodologies;
Fluency in local language and excellent English are required.
Medpace Overview
Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV 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 its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 6,000 people across 50+ countries.
Why Medpace?
People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.
The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.
Medpace Perks
Flexible work environment
Competitive compensation and benefits package
Competitive PTO packages
Structured career paths with opportunities for professional growth
Company-sponsored employee appreciation events
Employee health and wellness initiatives
Awards
Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023, 2024 and 2025
Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility
What to Expect Next
A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.
Responsibilities
Conduct feasibility, pre-study, initiation, monitoring, and closeout visits for research sites, mainly phase 1 to 3 and within all available therapeutic areas;
Perform source document verification and case report form review;
Perform regulatory document review;
Conduct study drug inventory;
Perform adverse event and serious adverse event reporting and follow-up; and
Assess patient recruitment and retention.
Qualifications
Bachelor of Science in health-related field;
Proven CRA experience of at least 1.5 years independent monitoring experience
Broad knowledge of medical terminology and clinical patient management;
Basic knowledge of drug therapy techniques and clinical research methodologies;
Fluency in local language and excellent English are required.
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Originally posted on Himalayas