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For Companies At a Glance
- Tasks: Monitor and manage clinical studies, ensuring compliance with protocols and regulations.
- Company: Join a passionate CRO with high CRA retention rates and a supportive culture.
- Benefits: Enjoy a flexible work-life balance, competitive salary, and opportunities for professional growth.
- Why this job: Make a real impact in oncology research while working from home in the UK.
- Qualifications: 2+ years of CRA experience; oncology experience is a plus.
- Other info: Collaborate with a dynamic team and influence meaningful outcomes in clinical trials.
The predicted salary is between 36000 - 60000 £ per year.
Clinical Research Associate II/Senior Clinical Research Associate
Remote, United Kingdom
Precision for Medicine is not your typical CRO. We are passionate about cultivating our culture and are proud to share extremely high CRA retention rates compared to industry averages.
CRAs join us, love their jobs, and stay because of the amazing people and enjoyable quality of life. You will have a lower than average number of protocols, setting you up to be a protocol expert. Travel is reasonable and your work/life balance will benefit as a result. Most meaningfully – your voice will be heard. Working in a smaller CRO allows you to have influence and impact when it matters most and support from direct line management.
We are hiring a CRA II/Senior CRA, this position will be fully home based working in the UK.
About you:
- You are calm, thoughtful, and responsive when things don’t go as planned.
- You are well-prepared, whether it be for an investigator meeting, site visit or project team update, always staying two steps ahead of the game.
- You find quick and creative ways of overcoming difficulties.
- You have an impeccable eye for detail.
- You identify potential study risks and propose solutions on how to mitigate them.
- You take responsibility in the quality and outcomes of your work.
- You are adept at handling conflict by using tried and true resolution strategies.
How we will keep you busy and support your growth:
You will monitor and own the progress of clinical studies at investigative sites and ensure that clinical studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and all applicable regulations and standards. You will coordinate all necessary activities required to set up and monitor a study (i.e., identify investigators; helping prepare regulatory submissions, conducting pre-study and initiation visits, etc.).
Qualifications:
- 4-year college degree or equivalent experience
- 4-year college degree or equivalent experience
- Candidates should have at least 2 years CRA experience within the CRO or pharmaceutical industry.
- Oncology experience, early phase experience desirable although not essential.
- Availability for domestic travel including overnight stays, which may constitute up to approximately 50-60% travel commitment (international travel may be required for some senior level positions)
- Fluency in English
Precision’s uniquely integrated offering enables the science of precision medicine by combining novel clinical trial designs, industry-leading operational and medical experts, advanced biomarker and data analytics solutions, and an unequivocal real passion for rare diseases and oncology.
Precision medicine is revolutionizing the attack on cancer—and we are passionate about helping you harness its power. We strike tumors on a molecular level using biomarkers to link specific mutations to specific treatments. We combine deep science with deep data from advanced technological platforms, then layer on specialized expertise in the design and execution of targeted, adaptive clinical trials. Ultimately, we deliver robust insights that inform real-time decisions—and optimize the oncology development pathway.
Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law.
If you require a reasonable accommodation to complete any part of the application process, you may contact us at the provided HR contact.
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Clinical Research Associate II/Senior Clinical Research Associate employer: Precision Medicine Group
Contact Detail:
Precision Medicine Group Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Research Associate II/Senior Clinical Research Associate
✨Tip Number 1
Network like a pro! Reach out to your connections in the clinical research field, attend industry events, and join relevant online groups. The more people you know, the better your chances of hearing about job openings before they even hit the market.
✨Tip Number 2
Prepare for interviews by researching the company and its culture. Understand their values and how they align with yours. This will help you answer questions confidently and show that you're genuinely interested in being part of their team.
✨Tip Number 3
Practice your responses to common interview questions, especially those related to problem-solving and conflict resolution. Use the STAR method (Situation, Task, Action, Result) to structure your answers and highlight your experience effectively.
✨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 take the initiative to connect directly with us.
We think you need these skills to ace Clinical Research Associate II/Senior Clinical Research Associate
Some tips for your application 🫡
Show Your Passion for Clinical Research: When writing your application, let your enthusiasm for clinical research shine through. We want to see how much you care about making a difference in the field, especially in oncology and rare diseases. Share any relevant experiences that highlight your commitment!
Be Detail-Oriented: Given the importance of detail in our work, make sure your application is free from typos and errors. We appreciate candidates who take the time to proofread their submissions. A polished application reflects your attention to detail, which is crucial for a CRA role.
Tailor Your Application: Don’t just send a generic application! Take the time to tailor your CV and cover letter to match the job description. Highlight your relevant experience and skills that align with what we’re looking for in a Clinical Research Associate II/Senior CRA.
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 shows you’re proactive and keen to join our team!
How to prepare for a job interview at Precision Medicine Group
✨Know Your Protocols
Before the interview, make sure you’re familiar with the protocols relevant to the role. Precision for Medicine values protocol expertise, so being able to discuss specific studies or methodologies will show that you’re prepared and knowledgeable.
✨Showcase Your Problem-Solving Skills
Be ready to share examples of how you've overcome challenges in previous roles. Since the job requires quick and creative solutions, having a couple of solid stories up your sleeve will demonstrate your ability to think on your feet.
✨Highlight Your Attention to Detail
As a Clinical Research Associate, an eye for detail is crucial. Bring up instances where your meticulous nature has positively impacted a project. This will resonate well with the interviewers who are looking for someone who takes responsibility for quality outcomes.
✨Prepare for Conflict Resolution Questions
Expect questions about handling conflicts or difficult situations. Think of specific strategies you’ve used in the past and be ready to explain how they worked. This will show that you can maintain a calm and thoughtful approach, which is essential for this role.