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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 flexibility, career development opportunities, and a supportive team environment.
- Why this job: Join a vital role in drug development with exciting challenges and a focus on work-life balance.
- Qualifications: Experience in site management and oncology trials, strong organisational skills, and knowledge of clinical research.
- Other info: Register your interest for upcoming roles and join our talent community for job alerts.
The predicted salary is between 36000 - 60000 £ per year.
***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 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
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Dedicated to one client.
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Responsible for all site management and monitoring activities across assigned oncology studies
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Work with industry leaders and subject matter experts.
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Opportunity to mentor junior CRAs.
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Work with world-class technology.
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a pivotal role in the drug development process.
Here are a few requirements specific to this advertised role.
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Substantial Site Management experience, with an understanding of the clinical
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trial methodology and terminology.
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Experience in, or willingness to monitor oncology clinical trials.
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Experience in independent monitoring, all types of visits.
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Effective time management, organizational and interpersonal skills & problem-solving skills, with the ability to multi-task and prioritize.
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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.
Not quite the role for you?
Join Our Talent Community and we’ll reach out with job alerts when positions that match your career interests become available. We’ll also share periodic updates about the latest company news and events.
Sign up today https://jobs.parexel.com/functional-service-provider
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Clinical Research Associate (Oncology) - South West England (Bristol; Bath; Bournemouth; Chelte[...] employer: Parexel International
Contact Detail:
Parexel International Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Research Associate (Oncology) - South West England (Bristol; Bath; Bournemouth; Chelte[...]
✨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. This can provide valuable insights and potentially lead to referrals.
✨Tip Number 2
Familiarise yourself with the latest trends and developments in oncology clinical trials. Subscribe to relevant journals or follow key opinion leaders on social media to stay updated. This knowledge can help you stand out during interviews and discussions.
✨Tip Number 3
Consider gaining additional certifications related to clinical research or oncology. This could enhance your qualifications and demonstrate your commitment to the field, making you a more attractive candidate for the role.
✨Tip Number 4
Prepare for potential interviews by practising common questions specific to Clinical Research Associates in oncology. Focus on your site management experience and how you've handled challenges in previous roles, as these will be crucial in showcasing your suitability for the position.
We think you need these skills to ace Clinical Research Associate (Oncology) - South West England (Bristol; Bath; Bournemouth; Chelte[...]
Some tips for your application 🫡
Understand the Role: Before applying, make sure you fully understand the responsibilities and requirements of the Clinical Research Associate position. Familiarise yourself with oncology clinical trials and the specific skills needed for this role.
Tailor Your CV: Customise your CV to highlight relevant experience in site management and oncology trials. Emphasise your understanding of clinical trial methodology, GCP/ICH guidelines, and any mentoring experience you may have.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for clinical research and your alignment with Parexel's values. Mention specific experiences that demonstrate your problem-solving skills and ability to manage multiple tasks effectively.
Proofread Your Application: Before submitting, carefully proofread your application materials. Check for any spelling or grammatical errors, and ensure that all information is accurate and presented professionally.
How to prepare for a job interview at Parexel International
✨Understand the Role
Make sure you have a solid grasp of what a Clinical Research Associate does, especially in oncology. Familiarise yourself with the specific responsibilities mentioned in the job description, such as site management and monitoring activities.
✨Showcase Relevant Experience
Prepare to discuss your previous experience in clinical trials, particularly any work related to oncology. Highlight your understanding of clinical trial methodology and your ability to manage multiple tasks effectively.
✨Demonstrate Problem-Solving Skills
Be ready to provide examples of how you've tackled challenges in past roles. This could include managing difficult situations at sites or resolving issues with protocols. Employers value candidates who can think on their feet.
✨Ask Insightful Questions
Prepare thoughtful questions about the company culture, the specific studies you'll be involved in, and opportunities for professional development. This shows your genuine interest in the role and helps you assess if it's the right fit for you.
