Oncology CRA II: Site Monitoring & Trials
Oncology CRA II: Site Monitoring & Trials

Oncology CRA II: Site Monitoring & Trials

Full-Time 35000 - 45000 £ / year (est.) No home office possible
IQVIA LLC

At a Glance

  • Tasks: Monitor clinical trial sites and ensure compliance with protocols.
  • Company: Join IQVIA, a leader in clinical research innovation.
  • Benefits: Flexible travel, competitive salary, and global impact on patient outcomes.
  • Other info: Dynamic role with opportunities for professional growth.
  • Why this job: Make a difference in oncology research and improve lives worldwide.
  • Qualifications: Life science degree and experience in clinical trials required.

The predicted salary is between 35000 - 45000 £ per year.

IQVIA LLC in Greater London seeks a Clinical Research Associate II, Oncology to accelerate innovation in clinical research. This full-time role involves site monitoring visits, managing trial protocols, and ensuring compliance with GCP and ICH guidelines.

Candidates should have a life science degree and experience with multiple clinical trials. The position requires flexibility to travel and offers an opportunity to contribute to improving patient outcomes globally.

Oncology CRA II: Site Monitoring & Trials employer: IQVIA LLC

IQVIA LLC is an exceptional employer that fosters a collaborative and innovative work culture, dedicated to advancing clinical research in the heart of Greater London. Employees benefit from comprehensive training and development opportunities, enabling them to grow their careers while making a meaningful impact on patient outcomes worldwide. With a commitment to flexibility and work-life balance, IQVIA offers a unique environment where professionals can thrive and contribute to groundbreaking advancements in healthcare.
IQVIA LLC

Contact Detail:

IQVIA LLC Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Oncology CRA II: Site Monitoring & Trials

✨Tip Number 1

Network like a pro! Reach out to professionals in the oncology field on LinkedIn or at industry events. We can’t stress enough how valuable personal connections can be in landing that CRA role.

✨Tip Number 2

Prepare for those interviews by brushing up on your knowledge of GCP and ICH guidelines. We want you to shine when discussing your experience with clinical trials, so have some examples ready to share!

✨Tip Number 3

Don’t just apply anywhere; focus on companies that align with your values and career goals. We recommend checking out our website for tailored job listings that suit your skills and aspirations.

✨Tip Number 4

Follow up after interviews! A quick thank-you email can go a long way in showing your enthusiasm for the role. We believe it’s a great way to keep you top of mind for hiring managers.

We think you need these skills to ace Oncology CRA II: Site Monitoring & Trials

Site Monitoring
Trial Protocol Management
GCP Compliance
ICH Guidelines Knowledge
Life Science Degree
Clinical Trials Experience
Flexibility to Travel
Patient Outcomes Improvement

Some tips for your application 🫡

Tailor Your CV: Make sure your CV highlights your experience in clinical trials and any relevant life science qualifications. We want to see how your background aligns with the role of Oncology CRA II, so don’t hold back on showcasing your skills!

Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re passionate about oncology and how your previous experiences make you a great fit for this role. We love seeing genuine enthusiasm for improving patient outcomes.

Showcase Your Flexibility: Since the role requires travel, mention any previous experiences where you’ve had to adapt quickly or manage multiple sites. We appreciate candidates who can demonstrate their flexibility and commitment to site monitoring.

Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it’s super easy – just follow the prompts!

How to prepare for a job interview at IQVIA LLC

✨Know Your Oncology Basics

Make sure you brush up on your oncology knowledge before the interview. Understand the latest trends in cancer research and be ready to discuss how they relate to clinical trials. This will show your passion for the field and your commitment to improving patient outcomes.

✨Familiarise Yourself with GCP and ICH Guidelines

Since compliance is key in this role, take some time to review Good Clinical Practice (GCP) and International Council for Harmonisation (ICH) guidelines. Be prepared to discuss how you've applied these in your previous roles, as it demonstrates your understanding of the regulatory landscape.

✨Highlight Your Trial Management Experience

Think about specific examples from your past experiences managing trial protocols. Be ready to share challenges you faced and how you overcame them. This will help the interviewers see your problem-solving skills and your ability to handle multiple trials effectively.

✨Show Your Flexibility and Travel Readiness

Since the role requires travel, be open about your flexibility. Share any previous experiences where you had to adapt quickly to changing schedules or locations. This will reassure the interviewers that you're ready for the demands of the job.

Oncology CRA II: Site Monitoring & Trials
IQVIA LLC

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