Clinical Research Associate, Maternity Leave Cover
Novo Nordisk
full-time
Posted on:
Location Type: Office
Location: Ørestad • 🇩🇰 Denmark
Visit company websiteJob Level
JuniorMid-Level
Tech Stack
Google Cloud PlatformVault
About the role
- manage clinical trial sites at every stage of the clinical trial process
- collaborate closely with clinical investigative site teams
- conduct and document monitoring visits in accordance with the Monitoring Plan
- drive activities with sites to achieve recruitment and retention targets
- manage protocol compliance, IMP handling and data entry requirements at site
- travel approximately 30% of the time including some overnight stays
Requirements
- Bachelor's Degree level, life science or nursing qualification or other relevant experience
- excellent understanding of clinical trial procedures – ICH GCP, regulatory issues, SOPs
- GCP Certification
- Knowledge of drug development process
- Good working knowledge of electronic clinical trials systems – Veeva Vault, EDC, IWRS, electronic TMF
- Excellent level of Danish and English
Benefits
- strong learning and development opportunities tailored to your career and life stage
- unique and supportive culture
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard skills
clinical trial managementmonitoring visitsprotocol compliancedata entryrecruitment strategiesretention strategiesdrug development processelectronic clinical trials systems
Soft skills
collaborationcommunicationorganizational skills
Certifications
GCP Certification