Experienced Clinical Research Associate, CRA
Medpace
full-time
Posted on:
Location Type: Remote
Location: Remote • 🇩🇰 Denmark
Visit company websiteJob Level
JuniorMid-Level
About the role
- Conduct feasibility, pre-study, initiation, monitoring, and closeout visits for research sites, mainly phase 1 to 3 and within all 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
- Assess patient recruitment and retention
- Work on a Nordic team to accomplish tasks and projects instrumental to the company’s success
Requirements
- 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
- Excellent English
- Candidates can be based anywhere in Denmark (home-based)
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
- Recognition and awards (Forbes and CRO Leadership Awards)
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard skills
source document verificationcase report form reviewregulatory document reviewstudy drug inventoryadverse event reportingserious adverse event reportingpatient recruitmentpatient retentionclinical research methodologiesdrug therapy techniques
Soft skills
communicationteamworkorganizational skillsproblem-solvingattention to detailindependenceadaptabilityfluency in local languageEnglish proficiency
Certifications
Bachelor of Science in health-related field