At a Glance
- Tasks: Manage site relationships and ensure successful clinical trials while safeguarding patient wellbeing.
- Company: Join Parexel, a mission-driven team delivering life-changing treatments.
- Benefits: Enjoy competitive pay, world-class training, and reduced travel opportunities.
- Other info: Flexible, self-driven work culture with clear paths for career growth.
- Why this job: Make a real impact in healthcare while advancing your career in a supportive environment.
- Qualifications: Experience in clinical research and strong communication skills are essential.
The predicted salary is between 40500 - 49500 £ per year.
Overview
As a CRA at Parexel, you will go beyond traditional monitoring to safeguard patient wellbeing and ensure study success across UK sites.
You’ll manage site relationships, oversee quality from site identification to close-out, and resolve issues promptly.
You’ll collaborate with cross-functional teams to drive enrollment, maintain compliance, and support data integrity.
This role offers training, reduced travel, and broad exposure to therapeutic areas, with a clear path for career growth.
Join a mission-driven team that delivers life-changing treatments.
- Pay / Benefits
- bonus incentive program
- world-class training
- career advancement opportunities
- reduced travel compared to peers
- remote/UK decentralised setup
Responsibilities
- Conduct qualification, initiation, monitoring, and termination visits at assigned sites and generate visit reports
- Oversee study integrity and foster site relationships to enable successful trial delivery
- Protect human subjects by ensuring rights and well-being per protocol
- Develop patient recruitment strategies with clinical sites to meet enrollment timelines while complying with SOPs, protocol amendments, GCP, and regulatory requirements
- Evaluate data quality, site efficacy, and drug accountability
- Perform site document verification and regulatory documentation checks
- Key requirements
- Site management or equivalent clinical research experience
- Ability to perform all clinical monitoring activities independently
- Strong written and verbal communication within a matrixed team
- Experience working in a self-driven, urgent, low-oversight environment
- Client-focused, flexible attitude toward assignments and learning
- Ability to manage multiple tasks and adhere to timelines while understanding study protocols
- Honest, ethical approach to developing life-changing treatments
- Strong computer skills including CTMS, EDMS, and MS Office
- Interpersonal skills
- Written and verbal communication
- Self-motivation
- Clinical Trial Management System (CTMS)
- Electronic Document Management System (EDMS)
- MS-Office suite (Excel, Word)
Clinical Research Associate II or Senior Clinical Research Associate in London employer: PAREXEL
At Parexel, we pride ourselves on being an exceptional employer, offering a collaborative work culture that fosters innovation and professional growth. Our team members enjoy competitive benefits, including flexible working arrangements and opportunities for career advancement, all while contributing to impactful global clinical trials in a supportive environment across the UK, Poland, Serbia, and Hungary.
