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Tech Stack
Tools & technologiesGoogle Cloud Platform
About the role
Key responsibilities & impact- Designing, planning, coordinating, and conducting activities involved in clinical research studies
- Acting as the primary contact and clinical trial expert
- Performing site assessments and qualification visits
- Developing and managing key study site documentation
- Overseeing CROs for delivery of site management activities
- Executing site management activities for sponsored studies
Requirements
What you’ll need- Bachelor's degree in Science Degree preferably in Health Sciences or engineering
- 3 years of working experience in either the Medical Device or Diagnostics industry
- 2 years of working experience in clinical study of IVD/Medical Device/Drug
- Experience particularly in the cardiovascular/metabolic indication and Near Patient Care or Point of Care
- Excellent understanding of ICH GCP guidelines in the execution of clinical trials
Benefits
Comp & perks- Health insurance
- Professional development opportunities
- Paid time off
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
clinical researchsite managementstudy site documentationsite assessmentsqualification visitsCRO managementclinical trial executionIVD studiesmedical device studiesdrug studies
Soft Skills
coordinationcommunicationplanningorganizationleadershipexpertise
Certifications
Bachelor's degreeICH GCP guidelines
