{"@context":"https:/schema.org/","@type":"JobPosting","title":"Clinical Research Associate (Onc[...]

Parexel; Bournemouth; Remote; GBP 35,000 - 50,000; Full time

Job summary

A leading clinical research organization is seeking a Clinical Research Associate based in South West England to manage and monitor oncology studies. This role offers long-term job security and opportunities for professional development within a supportive environment. Ideal candidates have substantial site management experience, effective organizational skills, and an understanding of clinical trials. Enjoy the flexibility of working from home while contributing to vital clinical studies.

Benefits

Flexible working hours

Opportunities for career development

Qualifications

• Understanding of clinical trial methodology and terminology.
• Willingness to monitor oncology clinical trials.
• Experience in independent monitoring across visits.

Responsibilities

• Manage all site management and monitoring activities for oncology studies.
• Work with industry leaders and subject matter experts.
• Mentor junior CRAs.

Skills

Site Management experience

Effective time management

Organizational skills

Interpersonal skills

Problem-solving skills

Job description

Clinical Research Associate (Oncology) - South West England

REGISTER YOUR INTEREST FOR UPCOMING CRA ROLES IN SOUTH WEST ENGLAND

Parexel is seeking Clinical Research Associates home-based in South West England to cover trials in the region. Working as a Clinical Research Associate at Parexel FSP offers long-term job security and prospects. We undertake vital clinical studies for sponsors including leading global biotechs and Pharma top 50, and we maintain 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, there is a world of opportunity. 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.

Responsibilities

• 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.

Requirements

• 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 we provide an open and friendly work environment where we empower people and provide opportunities to develop their long-term careers. 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.

About 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, and 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.