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- Tasks: Manage site activities and monitor oncology studies for a leading sponsor.
- 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 drug development 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.
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 the leading global biotechs and Pharma top 50. Our CRAs work from their home office base, supporting studies within their country or region.
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. You’ll be an influential member of the wider team.
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Senior Clinical Research Associate - Oncology Experience Required - UK (North/Midlands) - FSP employer: Parexel International
Contact Detail:
Parexel International Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Clinical Research Associate - Oncology Experience Required - UK (North/Midlands) - FSP
✨Tip Number 1
Make sure to highlight your oncology experience during networking events or industry meet-ups. Engaging with professionals in the field can lead to valuable connections and insights about the role.
✨Tip Number 2
Consider reaching out to current or former Clinical Research Associates at Parexel via LinkedIn. They can provide first-hand information about the company culture and expectations, which can be beneficial for your application.
✨Tip Number 3
Stay updated on the latest trends and advancements in oncology clinical trials. This knowledge can help you stand out during interviews and demonstrate your commitment to the field.
✨Tip Number 4
Prepare to discuss specific examples of your site management experience and how you've effectively handled challenges in previous roles. This will showcase your problem-solving skills and readiness for the responsibilities of the position.
We think you need these skills to ace Senior Clinical Research Associate - Oncology Experience Required - UK (North/Midlands) - FSP
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your oncology experience and relevant skills. Use specific examples from your past roles that demonstrate your site management and monitoring capabilities.
Craft a Compelling Cover Letter: Write a cover letter that addresses why you are interested in the Senior Clinical Research Associate position at Parexel. Mention your passion for oncology and how your experience aligns with their requirements.
Highlight Relevant Experience: In your application, emphasise your substantial site management experience and understanding of clinical trial methodology. Be specific about your independent monitoring experience and any oncology trials you've worked on.
Showcase Soft Skills: Parexel values effective time management, organisational skills, and problem-solving abilities. Include examples in your application that demonstrate these skills, particularly in a clinical research context.
How to prepare for a job interview at Parexel International
✨Showcase Your Oncology Experience
Make sure to highlight your specific oncology experience during the interview. Discuss any relevant clinical trials you've worked on, the roles you played, and how they relate to the responsibilities of the Senior Clinical Research Associate position.
✨Demonstrate Site Management Skills
Prepare examples that showcase your site management experience. Be ready to discuss how you've effectively managed sites, dealt with challenges, and ensured compliance with clinical trial protocols.
✨Familiarise Yourself with GCP/ICH Guidelines
Brush up on Good Clinical Practice (GCP) and International Council for Harmonisation (ICH) guidelines. Being able to discuss these in detail will show your understanding of the regulatory environment and your commitment to maintaining high standards in clinical research.
✨Emphasise Problem-Solving Abilities
Prepare to discuss specific instances where you've successfully solved problems in a clinical setting. Highlight your organisational skills and ability to prioritise tasks, as these are crucial for managing multiple studies effectively.
