Senior Clinical Research Associate
Parexel
full-time
Posted on:
Location Type: Remote
Location: Taiwan
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Job Level
Tech Stack
About the role
- Contributes to the selection of potential investigators
- Responsible for study start-up and regulatory maintenance
- Ensures the sites are always inspection ready
- Manages study supplies and drug accountability at study site
- Performs monitoring visits and Source Data Review
Requirements
- Bachelor’s degree in related discipline, preferably in life science
- Excellent knowledge of international guidelines ICH-GCP
- Basic knowledge of GMP/GDP
- Good medical knowledge and ability to learn relevant Client Therapeutic Areas
- Basic understanding of the drug development process
- Good understanding of Clinical Study Management including monitoring, study drug handling and data management
- Ability to travel nationally/internationally as required
Benefits
- Health insurance
- Flexible working hours
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
study start-upregulatory maintenancemonitoring visitsSource Data Reviewstudy drug handlingdata managementdrug development process
Soft Skills
ability to learngood medical knowledgeability to travel
Certifications
Bachelor’s degree