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- Tasks: Manage site activities and monitor oncology studies from home.
- Company: Parexel is a leader in clinical research, partnering with top biotechs and pharma companies.
- Benefits: Enjoy remote work, long-term job security, and opportunities for career growth.
- Why this job: Be part of vital drug development while maintaining a healthy work-life balance.
- Qualifications: Experience in site management and oncology trials is preferred; strong organisational skills are essential.
- Other info: Join a supportive team and mentor junior CRAs while working with cutting-edge technology.
The predicted salary is between 36000 - 60000 £ per year.
Parexel is currently seeking Clinical Research Associates, ideally with Oncology experience, based in South West England. Suitable locations could be Bath, Bristol, Bournemouth, Cheltenham, Exeter or Gloucester. This will be a home-based position and fully dedicated to a single sponsor.
Working as a Clinical Research Associate at Parexel 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.
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.
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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Clinical Research Associate II (Oncology) - South West England (Bristol; Bath; Bournemouth; Che[...] employer: Parexel International
Contact Detail:
Parexel International Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Research Associate II (Oncology) - South West England (Bristol; Bath; Bournemouth; Che[...]
✨Tip Number 1
Network with professionals in the oncology field. Attend relevant conferences or webinars to connect with current Clinical Research Associates and industry leaders. This can provide you with insights into the role and potentially lead to referrals.
✨Tip Number 2
Familiarise yourself with the latest trends and developments in oncology clinical trials. Being knowledgeable about current studies and methodologies will help you stand out during interviews and discussions with potential employers.
✨Tip Number 3
Consider reaching out to current or former employees of Parexel on platforms like LinkedIn. Ask them about their experiences and any tips they might have for succeeding in the application process or the role itself.
✨Tip Number 4
Prepare for potential interview questions by practising your responses to common scenarios faced by Clinical Research Associates. Focus on your problem-solving skills and how you've managed time and priorities in past roles.
We think you need these skills to ace Clinical Research Associate II (Oncology) - South West England (Bristol; Bath; Bournemouth; Che[...]
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in clinical research, particularly in oncology. Use specific examples of your site management and monitoring activities to demonstrate your expertise.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for clinical research and your understanding of the oncology field. Mention why you are interested in working with Parexel and how your skills align with their needs.
Highlight Relevant Skills: In your application, emphasise your effective time management, organisational skills, and problem-solving abilities. Provide examples of how you've successfully managed multiple tasks in previous roles.
Showcase Continuous Learning: Mention any ongoing education or training related to clinical trials, GCP/ICH guidelines, or oncology. This shows your commitment to professional development and staying updated in the field.
How to prepare for a job interview at Parexel International
✨Showcase Your Oncology Knowledge
Make sure to brush up on your oncology knowledge before the interview. Be prepared to discuss specific trials or studies you’ve worked on, and demonstrate your understanding of the unique challenges in oncology research.
✨Highlight Site Management Experience
Since the role requires substantial site management experience, be ready to share examples of how you've effectively managed sites in previous roles. Discuss your approach to monitoring and any successful strategies you've implemented.
✨Demonstrate Problem-Solving Skills
Prepare to discuss scenarios where you faced challenges during clinical trials and how you resolved them. This will showcase your problem-solving skills and ability to handle the complexities of clinical research.
✨Emphasise Time Management Abilities
Given the need for effective time management in this role, be ready to explain how you prioritise tasks and manage your workload. Share specific tools or methods you use to stay organised and ensure deadlines are met.
