Senior Clinical Research Associate

Parexel

Senior Clinical Research Associate managing clinical studies for Parexel. Ensuring compliance, performing site visits, and contributing to successful patient trials.

Posted 4/16/2026full-timeRemote • 🇹🇼 TaiwanSeniorWebsite

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

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

What you’ll need

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

Comp & perks

Health insurance
Flexible working hours

ATS Keywords

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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