Senior Clinical Research Associate - Oncology Experience Required - UK - FSP

Parexel International; United Kingdom; Remote; GBP 40,000 - 70,000; Full time

Job summary

An established industry player is seeking a Senior Clinical Research Associate based in the UK to support vital oncology studies. This role offers long-term job security and prospects, allowing you to work closely with leading biotechs and Pharma companies. As a CRA, you will manage site activities, ensuring effective monitoring and compliance with clinical trial standards. Enjoy a balanced work-life with manageable protocols while contributing to groundbreaking studies that impact patient well-being. This is an exciting opportunity to grow within a supportive environment while making a meaningful difference in drug development.

Qualifications

• 12 months recent oncology experience is essential.
• Understanding of clinical trial methodology and terminology.

Responsibilities

• Responsible for site management and monitoring activities.
• Mentor junior CRAs and work with industry leaders.

Skills

Site Management

Oncology Clinical Trials

Time Management

Organizational Skills

Interpersonal Skills

Problem-Solving Skills

Education

Bachelor's Degree in Life Sciences

Clinical Research Certification

Job description

Parexel is currently seeking a UK-based Senior Clinical Research Associate with at least 12 months recent oncology experience to join our team and be dedicated to a single sponsor.

Working as a Clinical Research Associate at Parexel FSP offers tremendous long-term job security and prospects. We undertake vital clinical studies for sponsors including the leading global biotechs and Pharma top 50. And we have an incredible pipeline of work.

Whether you see your future path as a CRA, or in fields such as clinical operations, project management, line management, or other positions, we have a world of opportunity waiting for you.

Our CRAs work from their home office base, supporting studies within their country or region. ‘Manageable sites, manageable protocols’ is our mantra. Expect exciting professional challenges in inspiring studies, but with time for your outside life.

Although this role can be bases anywhere in the UK, it's preferable for candidates to be based in the North.

Some specifics about this advertised role

• Dedicated to one client.

• Responsible for all site management and monitoring activities across assigned oncology studies

• Work with industry leaders and subject matter experts.

• Opportunity to mentor junior CRAs.

• Work with world-class technology.

• a pivotal role in the drug development process.

Here are a few requirements specific to this advertised role.

• Substantial Site Management experience, with an understanding of the clinical

• trial methodology and terminology.

• Experience in, or willingness to monitor oncology clinical trials.

• Experience in independent monitoring, all types of visits.

• Effective time management, organizational and interpersonal skills & problem-solving skills, with the ability to multi-task and prioritize.

• Good understanding and working knowledge of clinical research, phases of clinical trials, current GCP/ICH & country clinical research law & guidelines.

We care about our people and your passion, as they are the key to our success, and provide an open and friendly work environment where we empower people and provide them with opportunities to develop their long-term careers. In addition, you will have the opportunity to develop within your role and tackle further responsibilities or develop your skill set within other related departments of Parexel.

Who are Parexel

Parexel supports clinical studies across the full range of therapeutic areas, and we have longstanding partnerships with a vast client base.

We supported the trials of most of today’s top 50 best-selling drugs, but equally we enable more niche drug developments that are critical to the well-being of many patients.

You’ll be an influential member of the wider team.

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