Senior Clinical Research Associate – Remote Oncology Trials
Senior Clinical Research Associate – Remote Oncology Trials

Senior Clinical Research Associate – Remote Oncology Trials

Full-Time 45000 - 60000 £ / year (est.) Home office possible
Parexel International

At a Glance

  • Tasks: Ensure compliance and data integrity for oncology trials while coordinating with site personnel.
  • Company: Join Parexel International, a leader in clinical research.
  • Benefits: Remote work, competitive salary, and the chance to make a difference in healthcare.
  • Other info: Opportunity to grow in a dynamic and supportive environment.
  • Why this job: Be part of a dedicated team impacting cancer research and patient outcomes.
  • Qualifications: 4+ years in CRO or Pharma, with expertise in RECIST criteria.

The predicted salary is between 45000 - 60000 £ per year.

Parexel International is hiring a Senior Clinical Research Associate based in the UK. This role involves ensuring compliance with ICH GCP at clinical sites, coordinating with site personnel and ensuring data integrity for oncology trials.

The ideal candidate must have at least 4 years of experience in CRO or Pharma settings and expertise in RECIST criteria. The position offers a chance to work with a dedicated sponsor-focused team, serving critical roles in clinical research.

Senior Clinical Research Associate – Remote Oncology Trials employer: Parexel International

At Parexel International, we pride ourselves on being an exceptional employer, offering a collaborative and supportive work culture that empowers our employees to thrive in their careers. With a strong focus on professional development and growth opportunities, particularly in the dynamic field of oncology trials, we provide our team members with the resources they need to excel. Our remote working model allows for flexibility while being part of a dedicated sponsor-focused team, making a meaningful impact in clinical research.
Parexel International

Contact Detail:

Parexel International Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Senior Clinical Research Associate – Remote Oncology Trials

Tip Number 1

Network like a pro! Reach out to your connections in the clinical research field, especially those who have experience with oncology trials. A friendly chat can lead to insider info about job openings or even referrals.

Tip Number 2

Prepare for interviews by brushing up on ICH GCP guidelines and RECIST criteria. We want you to feel confident discussing these topics, as they’re crucial for the role. Practice common interview questions with a friend to nail your delivery.

Tip Number 3

Showcase your experience! When you get the chance to speak with potential employers, highlight your past roles in CRO or Pharma settings. Use specific examples of how you ensured data integrity and compliance at clinical sites.

Tip Number 4

Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we love seeing candidates who are proactive about their job search!

We think you need these skills to ace Senior Clinical Research Associate – Remote Oncology Trials

ICH GCP Compliance
Data Integrity
Oncology Trials
RECIST Criteria
Clinical Research Experience
CRO Experience
Pharma Experience
Site Coordination
Communication Skills
Attention to Detail
Problem-Solving Skills
Team Collaboration
Regulatory Knowledge

Some tips for your application 🫡

Tailor Your CV: Make sure your CV highlights your experience in CRO or Pharma settings, especially focusing on oncology trials. We want to see how your background aligns with the role, so don’t be shy about showcasing your expertise in RECIST criteria!

Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re passionate about clinical research and how you can contribute to our dedicated sponsor-focused team. Keep it engaging and relevant to the job description.

Showcase Compliance Knowledge: Since this role involves ensuring compliance with ICH GCP, make sure to mention any specific experiences or training you have in this area. We love candidates who understand the importance of data integrity in clinical trials!

Apply Through Our Website: We encourage you to apply directly through our website for a smoother application process. It’s the best way for us to receive your application and get to know you better!

How to prepare for a job interview at Parexel International

Know Your Oncology Inside Out

Make sure you brush up on your knowledge of oncology trials and RECIST criteria. Being able to discuss these topics confidently will show that you're not just familiar with the basics, but that you truly understand the nuances of the field.

Demonstrate Compliance Knowledge

Since compliance with ICH GCP is crucial for this role, prepare examples from your past experience where you ensured adherence to these guidelines. This will highlight your attention to detail and commitment to quality in clinical research.

Showcase Your Teamwork Skills

This position involves coordinating with site personnel, so be ready to share specific instances where you've successfully collaborated with others. Emphasise your ability to work within a sponsor-focused team and how you’ve contributed to achieving common goals.

Prepare Questions for Them

Interviews are a two-way street! Prepare thoughtful questions about their oncology trials and team dynamics. This not only shows your interest in the role but also helps you gauge if the company culture aligns with your values.

Senior Clinical Research Associate – Remote Oncology Trials
Parexel International

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