Clinical Research Associate (Oncology) - South West England (Bristol; Bath; Bournemouth; Chelte[...]

TN United Kingdom; Uxbridge; Remote; GBP 40,000 - 80,000; Full time

Job summary

An established industry player is seeking dedicated Clinical Research Associates to join their team, offering a home-based position that ensures work-life balance while managing critical oncology studies. This role provides long-term growth opportunities and the chance to work with leading global biotechs. You'll be pivotal in drug development, mentoring junior colleagues, and leveraging advanced technology. With a commitment to a friendly and supportive environment, this position is perfect for those passionate about making a difference in clinical research.

Qualifications

• Substantial site management experience and understanding of clinical trial methodology.
• Strong organizational, interpersonal, and problem-solving skills.

Responsibilities

• Managing all site activities for oncology studies.
• Mentoring junior CRAs and collaborating with industry leaders.
• Utilizing advanced technology in drug development.

Skills

Site Management

Clinical Trial Methodology

Organizational Skills

Interpersonal Skills

Problem-Solving Skills

Multitasking

Job description

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Client: Parexel

Location: Uxbridge, United Kingdom

Job Category: Other

EU work permit required: Yes

Job Reference: 70ad6bc89332

Job Views: 3

Posted: 10.05.2025

Expiry Date: 24.06.2025

Job Description:

When our values align, there's no limit to what we can achieve.

Parexel is currently seeking Clinical Research Associates based in South West England, with suitable locations including Bath, Bristol, Bournemouth, Cheltenham, Exeter, or Gloucester.

This is a home-based position dedicated to a single sponsor.

Working as a Clinical Research Associate at Parexel offers long-term job security and growth prospects. We conduct vital clinical studies for sponsors, including leading global biotechs and Pharma top 50, with an impressive pipeline of work.

Whether your future path is as a CRA or in clinical operations, project management, line management, or other roles, we offer a world of opportunities.

Our CRAs work from their home office, supporting studies within their country or region, following the mantra: ‘Manageable sites, manageable protocols’. Expect challenging studies balanced with time for your personal life.

Key aspects of this role include:

• Dedicated to one client.
• Managing all site activities for oncology studies.
• Collaborating with industry leaders and experts.
• Mentoring junior CRAs.
• Utilizing advanced technology.
• Playing a pivotal role in drug development.

Specific requirements include:

• Substantial site management experience and understanding of clinical trial methodology.
• Willingness to monitor oncology trials.
• Experience with independent monitoring and various visit types.
• Strong organizational, interpersonal, and problem-solving skills, with the ability to multitask.
• Knowledge of clinical research phases, GCP/ICH guidelines, and country-specific laws.

We value our people and your passion, providing an open, friendly environment that fosters career development. Opportunities to grow within your role or explore other departments are available.

About Parexel

Parexel supports clinical studies across therapeutic areas, with longstanding partnerships and a history of supporting top-selling drugs as well as niche developments vital to patient well-being.

You will be an influential member of our team.