Clinical Research Associate I/II/Senior – FSP
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
- Trains, supports, and advises Investigators and site staff in study related matters
- Ensures the sites are inspection ready at all times
- Initiates, monitors, and closes study sites in compliance with Client Procedural Documents
- Drives performance at the sites
- Performs monitoring visits (remote and onsite)
- Follows up on outstanding actions with study sites to ensure resolution in a timely manner
- Ensures compliance with the Client’s Code of Ethics and company policies
Requirements
- Bachelor’s degree in related discipline, preferably in life science, or equivalent qualification
- Excellent attention to detail
- Good written and verbal communication skills
- Good collaboration and interpersonal skills
- Good negotiation skills
- Proficient in written and spoken English language required
- Fluency in local language(s) required
- Excellent knowledge of international guidelines ICH-GCP, basic knowledge of GMP/GDP
- Good knowledge of relevant local regulations
- 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
Benefits
- Valid driving license per country requirements, as applicable.
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
monitoring visitsstudy managementdata managementdrug development processGMPGDPICH-GCPinvestigator trainingsite compliancestudy site initiation
Soft Skills
attention to detailwritten communicationverbal communicationcollaborationinterpersonal skillsnegotiation skillstimely resolutionadvisingsupportingperformance driving