At a Glance
- Tasks: Manage and monitor clinical trials, ensuring patient safety and quality execution.
- Company: Join Parexel, a leader in improving global health through innovative clinical solutions.
- Benefits: Competitive salary, professional development, and the chance to make a real difference.
- Other info: Work in a supportive environment with opportunities for growth in the healthcare sector.
- Why this job: Be part of a team that impacts patient lives and contributes to groundbreaking therapies.
- Qualifications: Bachelor’s degree in life sciences and 3.5 years of clinical research monitoring experience.
The predicted salary is between 46000 - 52000 £ per year.
When our values align, there's no limit to what we can achieve. At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do. Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.
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 employer: Parexel
At Parexel, we pride ourselves on fostering a collaborative and empathetic work culture that prioritises patient well-being above all else. As a Senior Clinical Research Associate, you will not only contribute to groundbreaking clinical trials but also benefit from extensive professional development opportunities and a supportive environment that values your expertise in oncology. Located in the heart of the EU, our team is dedicated to making a meaningful impact on global health, ensuring that every employee feels valued and empowered to make a difference.
StudySmarter Expert Advice🤫
We think this is how you could land Senior Clinical Research Associate - Sponsor Dedicated - Oncology Experience Needed
✨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 clinical trial methodologies and regulations. We recommend practising common interview questions related to site management and patient safety to show you mean business.
✨Tip Number 3
Don’t underestimate the power of follow-ups! After an interview, drop a quick thank-you email to express your appreciation. It keeps you fresh in their minds and shows your enthusiasm for the role.
✨Tip Number 4
Apply directly through our website! It’s the best way to ensure your application gets seen by the right people. Plus, it shows you’re genuinely interested in joining our mission to improve global health.
We think you need these skills to ace Senior Clinical Research Associate - Sponsor Dedicated - Oncology Experience Needed
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Senior Clinical Research Associate role. Highlight your relevant experience in oncology and clinical trial methodologies, as this will show us you’re a perfect fit for what we need.
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Share your passion for improving patient health and how your values align with ours at Parexel. We want to see your personality come through!
Showcase Your Experience:Don’t just list your previous roles; explain how your experience has prepared you for this position. Mention specific projects or trials you've worked on that relate to site management and 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 don’t miss out on any important updates from us!
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 recent advancements in cancer treatments and clinical trial methodologies. This will not only show your expertise but also your genuine interest in the field.
✨Demonstrate Your Empathy
Since Parexel values empathy, be prepared to share examples of how you've put patient well-being first in your previous roles. Think about specific situations where your actions positively impacted patient safety or study execution.
✨Be Ready for Regulatory Questions
Expect questions about ICH/GCP guidelines and local regulations. Brush up on these topics and be ready to discuss how you've applied them in your past experiences. This will demonstrate your thorough understanding of the compliance aspects of clinical trials.
✨Showcase Your Teamwork Skills
As a Senior CRA, you'll need to interface with various teams. Prepare to discuss how you've effectively communicated and collaborated with study teams, vendors, and investigator sites in the past. Highlight any challenges you faced and how you overcame them to ensure smooth operations.
