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

Parexel; London Borough of Harrow; Remote; GBP 60,000 - 80,000; Full time

Job summary

A leading clinical research company in Harrow is seeking Clinical Research Associates to manage oncology studies for regional trials in South West England. The role offers work-life balance, professional challenges, and opportunities for career development. Candidates should have experience in site management and clinical trial methodology. Join a team that contributes to significant drug developments and supports top global biotechs.

Qualifications

• Experience in site management and understanding of clinical trial methodology.
• Willingness to monitor oncology trials.
• Strong organizational skills.

Responsibilities

• Responsible for site management and monitoring of oncology studies.
• Collaborate with industry leaders and experts.
• Potential to mentor junior CRAs.

Skills

Site management

Interpersonal skills

Problem-solving skills

Multitasking

Job description

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Client:

Parexel

Location:

Harrow, United Kingdom

Job Category:

Other

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EU work permit required:

Yes

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Job Reference:

1e6835032dec

Job Views:

6

Posted:

12.08.2025

Expiry Date:

26.09.2025

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Job Description:

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

***REGISTER YOUR INTEREST FOR UPCOMING CRA ROLES IN SOUTH WEST ENGLAND***

Parexel is seeking Clinical Research Associates based in South West England to support regional trials.

Working as a Clinical Research Associate at Parexel FSP offers long-term job security and growth opportunities. We conduct vital clinical studies for sponsors, including top global biotechs and pharmaceutical companies, with an extensive pipeline of work.

Whether your goal is to become a CRA or to pursue roles in clinical operations, project management, or leadership, we have opportunities for you.

Our CRAs operate from their home offices, supporting studies within their region. We emphasize manageable sites and protocols, providing professional challenges with work-life balance.

Role specifics

Dedicated to a single client.

Responsible for site management and monitoring of oncology studies.

Collaborate with industry leaders and experts.

Potential to mentor junior CRAs.

Utilize advanced technology.

Play a pivotal role in drug development.

Requirements

Experience in site management and understanding of clinical trial methodology.

Willingness to monitor oncology trials.

Experience in 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 relevant laws.

We value our people and offer a supportive environment with opportunities for career development and skill enhancement.

About Parexel

Parexel supports a wide range of therapeutic areas and has longstanding client partnerships.

We have contributed to trials for most of today’s top 50 drugs and support niche developments critical to patient well-being.

You will be a key member of our team.