Experienced Clinical Research Associate, CRA (Home-Based opportunities available)

Medpace, Inc.; Denmark; On-site; DKK 420,000 - 540,000; Full time

Benefits offered by this job

Flexible work environment

Competitive compensation and benefits

Competitive PTO

Structured career paths

Employee appreciation events

Wellness initiatives

Job summary

Medpace, Inc. is seeking full-time, home-based Clinical Research Associates to join our Clinical Operations team in Denmark.

Candidates can be based anywhere in Denmark and will work on a Nordic team on studies across multiple therapeutic areas. The role involves feasibility and site monitoring visits, data verification, regulatory reviews, drug inventory, AE/SAE reporting, and patient recruitment assessment.

Qualifications

• Bachelor of Science in a health-related field is required.
• At least 1.5 years independent CRA monitoring experience.
• Broad knowledge of medical terminology and clinical patient management.
• Basic knowledge of drug therapy techniques and clinical research methodologies.
• Fluency in Danish and English is required.

Responsibilities

• Conduct feasibility, pre-study, initiation, monitoring, and closeout visits for research sites (Phases 1–3).
• Perform source data verification and case report form review.
• Review regulatory documents and conduct study drug inventory.
• Report adverse events and follow-up on SAE events.
• Assess patient recruitment and retention.

Skills

Danish language

English language

CRA experience

Medical terminology

Clinical patient management

Education

Bachelor of Science in health-related field

Job description

Job Summary

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.

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.

Benefits

• 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