At a Glance
- Tasks: Manage and monitor clinical trials, ensuring patient safety and quality execution.
- Company: Parexel, a leader in clinical research with a focus on patient well-being.
- Benefits: Competitive salary, professional development, and the chance to impact patient lives.
- Other info: Be part of a supportive environment with opportunities for career growth.
- Why this job: Join a dynamic team and contribute to groundbreaking oncology research.
- Qualifications: Bachelor’s degree in life sciences and 3.5 years of clinical monitoring experience.
The predicted salary is between 40000 - 55000 £ per year.
Parexel FSP is hiring for an experienced Senior CRA level to join one of a large Sponsor’s in the EU. This role is responsible for the site management, site monitoring and close‑out of assigned clinical trials investigator sites to ensure patient safety and quality study execution.
Some Specifics About This Advertised Role:
- Ensure proper conduct of clinical trials in accordance with the Study Monitoring Plan and applicable prevailing laws, Good Clinical Practices.
- Manage assigned operational aspects for implementation of clinical trial activities at assigned investigator sites from site activation through database lock, ensuring relevant timelines and quality deliverables are met.
- Interface with the study team as needed, facilitate information flow between members of the study team, vendors and assigned investigator sites.
- Monitor site level AEs and SAEs and collaborate with the Drug Safety Unit and follow‑up with investigators sites, as needed, to bring SAE reports required information to resolution.
- Serve as a point of contact for audit conduct, and drive Audit Observation CAPA development and checks when applicable.
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.
What We Are Looking For In This Role:
For every role, we look for professionals who have the determination and courage always to put patient well‑being first. That to us is working with heart. Here are a few requirements specific to this advertised role:
- Bachelor’s degree in life sciences or professional degree in life sciences such as nursing, pharmacy, medical background or equivalent.
- Extensive knowledge of clinical trial methodologies, ICH/GCP, FDA and local country regulations.
- Monitoring Experience: Minimum 3.5 years relevant experience in clinical research site monitoring (preferably in Oncology).
- Preferred therapeutic experience in Oncology, Vaccines, Internal Medicine or Infectious Diseases.
Senior Clinical Research Associate - Sponsor Dedicated - Oncology Experience Needed in Uxbridge employer: Parexel
At Parexel, we pride ourselves on being an exceptional employer, offering a collaborative and supportive work culture that prioritises patient well-being and professional growth. As a Senior Clinical Research Associate, you will have the opportunity to work on groundbreaking oncology trials within a dynamic team, benefiting from extensive training and development programmes tailored to enhance your expertise in clinical research. Our commitment to innovation and excellence, combined with our strong partnerships across the pharmaceutical industry, makes Parexel a rewarding place to advance your career while making a meaningful impact on patients' lives.
StudySmarter Expert Advice🤫
We think this is how you could land Senior Clinical Research Associate - Sponsor Dedicated - Oncology Experience Needed in Uxbridge
✨Tip Number 1
Network like a pro! Reach out to your connections in the clinical research field, especially those with oncology experience. A friendly chat can lead to insider info about job openings or even a referral.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of ICH/GCP guidelines and local regulations. We want you to shine when discussing your monitoring experience and how it relates to patient safety.
✨Tip Number 3
Showcase your passion for patient well-being during interviews. Share examples of how you've put patients first in your previous roles. This will resonate with hiring managers who value heart in their team.
✨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 - Sponsor Dedicated - Oncology Experience Needed in Uxbridge
Some tips for your application 🫡
Tailor Your CV:Make sure your CV highlights your relevant experience in clinical research, especially in oncology. We want to see how your background aligns with the role, so don’t be shy about showcasing your skills and achievements!
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to explain why you’re passionate about clinical trials and patient safety. We love seeing candidates who can connect their personal motivations to the work we do.
Showcase Your Monitoring Experience:Since this role requires site monitoring experience, make sure to detail your past roles and responsibilities in this area. We’re looking for specifics on how you’ve managed trials and ensured compliance with regulations.
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 to do!
How to prepare for a job interview at Parexel
✨Know Your Oncology Stuff
Make sure you brush up on your oncology knowledge before the interview. Familiarise yourself with the latest trends, treatments, and clinical trial methodologies in this area. Being able to discuss specific studies or drugs will show your passion and expertise.
✨Understand the Regulations
Since this role involves ensuring compliance with ICH/GCP and local regulations, it’s crucial to have a solid understanding of these guidelines. Prepare to discuss how you've applied these in your previous roles, as this will demonstrate your readiness for the responsibilities of the position.
✨Showcase Your Monitoring Experience
With a minimum of 3.5 years of site monitoring experience required, be ready to share specific examples from your past work. Highlight challenges you faced, how you overcame them, and the impact of your actions on patient safety and study quality.
✨Be Ready for Team Dynamics
This role requires effective communication with various stakeholders. Think of examples where you facilitated information flow between teams or resolved conflicts. Showing that you can work collaboratively will be key to impressing the interviewers.
