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- Tasks: Conduct site visits, ensure compliance, and manage clinical trials.
- Company: Join a global CRO dedicated to innovative clinical research.
- Benefits: Remote work, career development, and a supportive team environment.
- Why this job: Make a real impact on patients' lives through groundbreaking research.
- Qualifications: 2+ years of clinical monitoring experience and strong communication skills.
- Other info: Diverse and inclusive workplace with excellent growth opportunities.
The predicted salary is between 36000 - 60000 £ per year.
We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence.
Our mission is to work with passion and purpose every day to improve lives and we are looking for others who value this same pursuit.
We believe everyone plays an important role in making a world of difference for patients and their caregivers. From our hands‑on, accessible leaders, to our cohesive and supportive teams, we are committed to enabling professionals from all backgrounds and experiences to succeed. We prioritize cultivating a diverse and inclusive environment that continues to promote collaboration and creativity.
As a Clinical Research Associate (CRA), you will find yourself working alongside brilliant minds across diverse therapeutic areas, including Cardiovascular, Metabolic, Neuroscience, Oncology, and Rare Diseases. Collaboration with top‑tier colleagues from various backgrounds and specialties is not just encouraged; it’s ingrained in our culture.
In a CRA role, you’ll receive extensive support through regulatory submissions, TMF management, and in‑house CRAs for projects with heavy site management needs. Through regular touchpoints and coaching conversations with your Line Manager, we ensure that your professional development remains a top priority. We offer a clear career path and development that can lead to Clinical Trial Manager roles.
What you will do:
- Conduct all types of visits – site qualifications, initiation, interim monitoring, site management and study close‑out visits
- Review study subject safety information and informed consent and conduct source document verification for compliance, patient safety, and veracity of data
- Actively participate in study team and investigator meetings
- Compile and ensure completeness of regulatory documents and ethical submission documentation
What you will bring to the role:
- Excellent interpersonal, oral, and written communication skills in English and local language
- Superior organizational skills with attention to detail, and the ability to work independently
- Broad understanding of clinical research principles and process
- Proficiency in Microsoft Office, CTMS, and EDC Systems
Your experience:
- At least two years of independent clinical monitoring experience
- Demonstrable experience in handling multiple protocols across a range of therapeutic indications
- Four‑year college curriculum in life sciences, OR Two‑year college curriculum or equivalent education/training (nursing degree or equivalent life science degree)
- Ability to meet the travel requirements of the job
We love knowing that someone is going to have a better life because of the work we do.
Contractor Senior Clinical Research Associate CNS/Oncology- UK - Remote employer: Worldwide Clinical Trials
Contact Detail:
Worldwide Clinical Trials Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Contractor Senior Clinical Research Associate CNS/Oncology- UK - Remote
✨Tip Number 1
Network like a pro! Reach out to your connections in the clinical research field, especially those who work at CROs. A friendly chat can lead to insider info about job openings or even a referral.
✨Tip Number 2
Prepare for interviews by researching the company culture and values. At Worldwide Clinical Trials, they value passion and purpose, so be ready to share how your experiences align with their mission.
✨Tip Number 3
Showcase your skills during interviews! Bring examples of how you've handled multiple protocols or ensured patient safety in past roles. This will demonstrate your expertise and fit for the CRA position.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, you’ll find all our latest roles there, so keep checking back for new opportunities!
We think you need these skills to ace Contractor Senior Clinical Research Associate CNS/Oncology- UK - Remote
Some tips for your application 🫡
Show Your Passion: When writing your application, let your passion for clinical research shine through. We want to see how your values align with our mission to improve lives and make a difference in the world.
Tailor Your CV: Make sure to customise your CV for the role. Highlight your relevant experience in clinical monitoring and any specific therapeutic areas you've worked in. We love seeing how your background fits with what we do!
Be Clear and Concise: Keep your application clear and to the point. Use straightforward language and avoid jargon. We appreciate when candidates can communicate effectively, just like we do in our teams!
Apply Through Our Website: Don’t forget to apply through our careers page! It’s the best way for us to receive your application and ensures you’re considered for the role. We can’t wait to hear from you!
How to prepare for a job interview at Worldwide Clinical Trials
✨Know Your Stuff
Make sure you brush up on your clinical research principles and processes. Familiarise yourself with the specific therapeutic areas mentioned in the job description, especially CNS and Oncology. This will show that you're not just interested in the role but also understand the complexities involved.
✨Showcase Your Communication Skills
Since excellent communication is key for this role, prepare to demonstrate your interpersonal skills during the interview. Think of examples where you've effectively communicated complex information or collaborated with diverse teams. This will highlight your ability to thrive in a supportive and team-oriented environment.
✨Be Ready for Scenario Questions
Expect questions that assess how you handle real-world situations in clinical monitoring. Prepare by thinking through past experiences where you managed multiple protocols or dealt with compliance issues. Use the STAR method (Situation, Task, Action, Result) to structure your answers clearly.
✨Ask Insightful Questions
At the end of the interview, don’t shy away from asking questions. Inquire about the team dynamics, professional development opportunities, or how the company fosters an inclusive environment. This shows your genuine interest in the role and the company culture, aligning with their mission to improve lives.
