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 work culture that values innovation and integrity. Our South West UK location provides a vibrant environment for professional growth, with ample opportunities for career advancement and continuous learning in the clinical research field. Employees enjoy a supportive atmosphere that prioritises work-life balance and fosters meaningful contributions to patient safety and study success.
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Some tips for your application 🫡
Showcase Your Relevant Experience:When applying for the Senior Clinical Research Associate - Sponsor Dedicated - Oncology Experience Needed at PAREXEL, focus on highlighting your clinical experience and any specific training you've undergone. Include any relevant placements or internships you’ve completed, as well as any certifications that bolster your qualifications in human medicine.
Highlight Your Soft Skills:In the field of human medicine, soft skills are just as crucial as technical knowledge. Mention your communication skills, empathy, and teamwork experiences in your CV and cover letter. This shows that you can work well in a clinical setting and with patients, which is super important in this industry!
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Include Continuing Education:Make sure to mention any ongoing education or courses you’re taking to keep your skills sharp. In human medicine, staying updated with the latest practices is key. It shows you’re dedicated to your field, which employers like PAREXEL will definitely appreciate!
How to prepare for a job interview at PAREXEL
✨Brush Up on Clinical Knowledge
Since you're aiming for a role in human medicine, make sure you’re sharp on the latest clinical guidelines and practices relevant to the position. Be prepared to discuss case studies or scenarios you might encounter in the role. This will show that you're not just knowledgeable but also ready to apply that knowledge in real-life situations.
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Ethics are a big deal in human medicine, so expect questions that assess your decision-making in tricky situations. Think about how you'd handle ethical dilemmas or patient confidentiality concerns. Prepare a few examples that illustrate your thought process and how you prioritise patient welfare in your decision-making.
