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For Companies At a Glance
- Tasks: Conduct clinical trials, manage site relationships, and ensure patient safety.
- Company: Join Parexel, a leader in biopharmaceutical services dedicated to improving global health.
- Benefits: Enjoy competitive pay, bonuses, flexible work, and top-notch training.
- Why this job: Make a real impact on patients' lives while advancing your career in clinical research.
- Qualifications: Experience in clinical research and strong communication skills required.
- Other info: Work in a supportive environment with opportunities for growth and development.
The predicted salary is between 36000 - 60000 ÂŁ per year.
Clinical Research Associate II or Senior Clinical Research Associate
Parexel Uxbridge, England, United Kingdom
Parexel is in the business of improving the world’s health. We do this by providing a suite of biopharmaceutical services that help clients across the globe transform scientific discoveries into new treatments. From clinical trials to regulatory, consulting, and market access, our therapeutic, technical, and functional ability is underpinned by a deep conviction in what we do. We believe in our values, Patients First, Quality, Respect, Empowerment & Accountability.
What You’ll Do
- Leverage your expertise. Conduct qualification visits (QV), site initiation visits (SIV), monitoring visits (MV) and termination visits (TV) at assigned clinical sites and generate visit/contact reports.
- Build relationships. Oversee integrity of the study and utilize problem‑solving skills to promote rapport with the site and staff.
- Protect patients. Review the performance of the trial at designated sites, ensure the rights and well‑being of human subjects are safeguarded and are in accordance with protocol.
- Drive productivity. Develop patient recruitment strategies in conjunction with the clinical site to meet enrollment timelines, while also ensuring compliance with the approved standard operating procedures (SOPs), protocol/amendment(s), GCP, and the applicable regulatory requirement(s).
- Ensure quality. Evaluate the quality and integrity of the reported data, site efficacy and drug accountability.
- Execute. Monitor the completeness and quality of Regulatory Documentation and perform site document verification.
More About You
- Site Management or equivalent experience in clinical research, with understanding of clinical trials methodology and terminology.
- Ability to perform all clinical monitoring activities independently.
- Bachelor’s or equivalent degree in biological science, pharmacy or other health related discipline.
- Strong interpersonal, written, and verbal communication skills within a matrixed team.
- Experience working in a self‑driven capacity, with a sense of urgency and limited oversight.
- A client‑focused approach to work and flexible attitude with respect to assignments/new learning.
- The ability to manage multiple tasks, evaluate a variety of unpredictable scenarios and achieve project timelines while being able to apply your understanding of study protocol(s).
- An honest and ethical work approach to promote the development of life‑changing treatments for patients.
- Strong computer skills, including but not limited to the knowledge of a Clinical Trial Management System (CTMS), Electronic Document Management System (EDMS) and MS‑Office products such as Excel and Word.
Seniority level
Entry level
Employment type
Full‑time
Job function
Health Care Provider, Science, and Research
Industries
Pharmaceutical Manufacturing, Biotechnology Research, and Hospitals and Health Care
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Clinical Research Associate II employer: Parexel
Contact Detail:
Parexel Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Research Associate II
✨Tip Number 1
Network like a pro! Reach out to professionals in the clinical research field on LinkedIn or at industry events. Building connections can lead to insider info about job openings and even referrals.
✨Tip Number 2
Prepare for interviews by researching Parexel's values and recent projects. Show us how your skills align with our mission to improve global health, and don’t forget to highlight your problem-solving abilities!
✨Tip Number 3
Practice makes perfect! Conduct mock interviews with friends or mentors to boost your confidence. Focus on articulating your experience in clinical trials and how you can contribute to patient safety and study integrity.
✨Tip Number 4
Don’t just apply anywhere; apply through our website! It’s the best way to ensure your application gets noticed. Tailor your CV and cover letter to reflect how you embody our values of Patients First, Quality, and Empowerment.
We think you need these skills to ace Clinical Research Associate II
Some tips for your application 🫡
Show Your Passion: When you're writing your application, let your passion for improving health shine through. We want to see how much you care about making a difference in patients' lives, so share your motivation and experiences that align with our values.
Tailor Your CV: Make sure your CV is tailored to the Clinical Research Associate II role. Highlight relevant experience, skills, and achievements that demonstrate your expertise in clinical trials and site management. We love seeing how your background fits with what we do!
Craft a Compelling Cover Letter: Your cover letter is your chance to tell us why you're the perfect fit for Parexel. Use it to elaborate on your experience, showcase your problem-solving skills, and explain how you can contribute to our mission of improving health. Keep it engaging and personal!
Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way to ensure your application gets into the right hands. Plus, you'll find all the details you need about the role and our company culture there!
How to prepare for a job interview at Parexel
✨Know Your Stuff
Make sure you brush up on clinical trial methodologies and terminology. Being able to speak confidently about your experience and how it relates to the role will show that you're not just a good fit, but that you genuinely understand the industry.
✨Build Rapport
Since the role involves building relationships with clinical sites, practice how you'll connect with your interviewers. Use examples from your past experiences where you've successfully managed site relationships or resolved issues, showcasing your interpersonal skills.
✨Showcase Problem-Solving Skills
Prepare to discuss specific challenges you've faced in previous roles and how you tackled them. This is crucial for a CRA position, as problem-solving is key to ensuring site success and patient safety.
✨Be Client-Focused
Demonstrate your client-focused approach by sharing instances where you've gone above and beyond for clients or stakeholders. Highlighting your flexibility and willingness to learn will resonate well with Parexel's values.
