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- Tasks: Manage site activities and monitor oncology studies for a leading client.
- Company: Join Parexel, a top player in clinical research with global partnerships.
- Benefits: Enjoy remote work flexibility, career development opportunities, and a supportive environment.
- Why this job: Be part of groundbreaking studies that impact patient lives while maintaining work-life balance.
- Qualifications: Must have 12 months oncology experience and strong site management skills.
- Other info: Opportunity to mentor junior CRAs and work with cutting-edge technology.
The predicted salary is between 36000 - 60000 £ per year.
When our values align, there's no limit to what we can achieve. Parexel is currently seeking Clinical Research Associates 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 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.
Senior Clinical Research Associate - Oncology Experience Required - UK - FSP employer: Parexel
Contact Detail:
Parexel Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Clinical Research Associate - Oncology Experience Required - UK - FSP
✨Tip Number 1
Network with professionals in the oncology field. Attend industry conferences, webinars, or local meetups to connect with current Clinical Research Associates and learn about their experiences at Parexel. This can provide you with valuable insights and potentially a referral.
✨Tip Number 2
Familiarise yourself with the latest trends and advancements in oncology clinical trials. Being knowledgeable about current research and methodologies will not only boost your confidence but also demonstrate your commitment to the field during interviews.
✨Tip Number 3
Prepare to discuss your site management experience in detail. Be ready to share specific examples of how you've effectively managed sites and monitored trials, as this is crucial for the role at Parexel. Highlight any challenges you faced and how you overcame them.
✨Tip Number 4
Showcase your problem-solving skills by preparing scenarios related to common issues in clinical trials. Think about how you would handle site-related challenges or protocol deviations, as this will illustrate your critical thinking abilities to the hiring team.
We think you need these skills to ace Senior Clinical Research Associate - Oncology Experience Required - UK - FSP
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your oncology experience and site management skills. Use specific examples from your previous roles to demonstrate your expertise in clinical trials and monitoring.
Craft a Compelling Cover Letter: Write a cover letter that reflects your passion for oncology and your understanding of the role. Mention how your values align with Parexel's and express your enthusiasm for contributing to their mission.
Highlight Relevant Skills: In your application, emphasise your effective time management, organisational skills, and problem-solving abilities. Provide concrete examples of how you've successfully managed multiple tasks in previous positions.
Follow Application Instructions: Carefully read the job posting and ensure you follow all application instructions. Submit all required documents and double-check for any specific requirements related to the role.
How to prepare for a job interview at Parexel
✨Showcase Your Oncology Experience
Make sure to highlight your specific experience in oncology during the interview. Discuss any relevant clinical trials you've worked on, the roles you played, and the outcomes of those studies. This will demonstrate your expertise and commitment to the field.
✨Understand Clinical Trial Methodology
Be prepared to discuss your understanding of clinical trial methodologies and terminology. Familiarise yourself with the phases of clinical trials and current GCP/ICH guidelines, as this knowledge is crucial for the role.
✨Demonstrate Problem-Solving Skills
Prepare examples of how you've effectively managed challenges in previous roles. Highlight your problem-solving skills and ability to prioritise tasks, as these are essential for managing multiple sites and protocols.
✨Express Your Passion for Clinical Research
Convey your enthusiasm for clinical research and the impact it has on patient care. Share why you want to work with Parexel specifically and how you align with their values, as cultural fit is important to them.
