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About the role
Key responsibilities & impact- Conduct all types of monitoring, and co-monitoring visits and associated monitoring activities for assigned clinical sites
- Ensure studies are conducted and documented in accordance with study protocols and regulatory requirements
- Responsible for monitoring report writing and completion
- Support development of study specific documentation related to monitoring activities
- Manage investigational supplies and monitor assigned clinical trials
- Communicate with assigned clinical sites and other stakeholders about study needs
- Participate in meetings and conference calls with project teams
Requirements
What you’ll need- Bachelor’s degree or equivalent combination of education and experience
- > 5 years of experience as a Clinical Research Associate
- Excellent verbal, written communication skills in Serbian and English
- Experience with Microsoft Office applications
- Electronic data capture (EDC), CTMS, IVRS, and eTMF experience
- Knowledge of local law, local regulatory requirements, and GCPs governing clinical trials
Benefits
Comp & perks- Health insurance
- 401(k) matching
- Flexible work hours
- Paid time off
- Remote work options
ATS Keywords
✓ Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
monitoring report writingclinical trial managementstudy protocol complianceinvestigational supply managementdocumentation developmentdata analysis
Soft Skills
communication skillsteam collaborationstakeholder engagementorganizational skillsproblem-solving
Certifications
Bachelor's degreeGood Clinical Practice (GCP) certification