Clinical Research Jobs | Apply at Paraxel Today
Clinical Research Jobs continue to grow rapidly as global organizations expand clinical operations and advance breakthrough therapies. This article explores the Clinical Research Associate II and Senior Clinical Research Associate roles at Parexel, highlighting responsibilities, skills, and opportunities within decentralized clinical trial environments. Whether you’re aiming to strengthen your expertise or searching for top Parexel jobs, this guide provides everything you need to know.
Job Details:
- Job Title: Clinical Research Associate II or Senior Clinical Research Associate
- Primary Location: United Kingdom, Remote
- Job ID: R0000036078
- Category: Clinical Trials
Clinical Research Job Overview
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Clinical research associate responsibilities include conducting QV, SIV, MV, and TV visits.
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CRAs build strong site relationships, oversee study integrity, and solve operational issues.
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Professionals in Parexel jobs ensure adherence to GCP, SOPs, and regulatory requirements.
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These Clinical Research Jobs provide access to world-class technology, reduced travel, and ongoing training.
What You’ll Do
- Leverage your expertise in conducting qualification, initiation, monitoring, and termination visits at clinical sites, generating reports.
- Build relationships and manage study integrity, safeguarding the well-being of human subjects per protocol.
- Boost productivity by developing recruitment strategies and ensuring protocol compliance.
- Evaluate reported data integrity, site efficacy, and drug accountability.
- Execute regulatory documentation monitoring and verification tasks.
Educational Requirements and Skills:
- Bachelor’s or equivalent degree in biological sciences or related health discipline
- Site Management or similar experience in clinical research with a thorough understanding of trial methodologies and terminology.
- Ability to independently carry out clinical monitoring tasks.
- Strong communication skills in a matrixed team setting.
- Experience working autonomously with urgency and minimal oversight.
- Client-focused approach, adaptability in assignments, and learning new skills.
- Capability to manage multiple tasks, handle unpredictable situations, and meet project timelines while understanding study protocols.
- An honest approach promoting life-changing treatment development for patients.
- Proficiency with computer systems, including CTMS, EDMS, and MS Office tools like Excel and Word.
