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- 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 competitive salary, work-life balance, and opportunities for professional growth.
- Why this job: Make a real impact in oncology research while working from home in the UK.
- Qualifications: 1+ years of CRA experience; oncology experience is a plus.
- Other info: Your voice matters here—contribute to meaningful change in cancer therapies.
The predicted salary is between 36000 - 60000 £ per year.
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.
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
- Other Required: Candidates should ideally have more than 1 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.
We invite you to learn more about our growing organization serving our clients that are researching groundbreaking cancer therapies. We strive to ensure employees feel appreciated for the contributions they make every single day. You will provide input and have your ideas valued and nurtured, impacting positive change for the company.
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 are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group.
It has come to our attention that some individuals or organizations are reaching out to job seekers and posing as potential employers presenting enticing employment offers. We want to emphasize that these offers are not associated with our company and may be fraudulent in nature. Please note that our organization will not extend a job offer without prior communication with our recruiting team, hiring managers and a formal interview process.
Clinical Research Associate II in London employer: Precision For Medicine
Contact Detail:
Precision For Medicine Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Research Associate II in London
✨Tip Number 1
Network like a pro! Reach out to your connections in the industry, especially those who work at Precision for Medicine. A friendly chat can open doors and give you insider info about the company culture and what they really value in a Clinical Research Associate.
✨Tip Number 2
Prepare for your interviews by diving deep into the specifics of the role. Brush up on your knowledge of oncology and clinical trials, and think of examples from your experience that showcase your attention to detail and problem-solving skills. We want to see how you handle challenges!
✨Tip Number 3
Show your passion for precision medicine! During interviews, express why you’re excited about the impact of clinical research on cancer therapies. Let us know how your values align with our mission, and don’t be shy about sharing your ideas on how to improve processes.
✨Tip Number 4
Apply through our website for the best chance of getting noticed. Tailor your application to highlight your relevant experience and skills, and make sure to follow up after submitting. A little persistence goes a long way in showing us you’re serious about joining our team!
We think you need these skills to ace Clinical Research Associate II in London
Some tips for your application 🫡
Show Your Passion: When you're writing your application, let your enthusiasm for clinical research shine through! We want to see that you’re genuinely excited about the role and how you can contribute to our mission in precision medicine.
Tailor Your CV: Make sure your CV is tailored to highlight your relevant experience as a Clinical Research Associate. Focus on your skills in monitoring studies, managing protocols, and any oncology experience you have. We love seeing how your background aligns with what we do!
Be Detail-Oriented: Since attention to detail is key in this role, ensure your application is free from typos and errors. A polished application reflects your meticulous nature, which is exactly what we’re looking for in a CRA II.
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 and shows us you’re serious about joining our team at Precision for Medicine!
How to prepare for a job interview at Precision For Medicine
✨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. Highlight your calm and thoughtful approach when things don’t go as planned, as this aligns perfectly with what they’re looking for in a Clinical Research Associate II.
✨Emphasise Your Attention to Detail
During the interview, mention specific instances where your eye for detail made a difference in your work. This could be anything from identifying potential study risks to ensuring compliance with regulations—demonstrating this skill is crucial for the role.
✨Engage and Ask Questions
Don’t forget that interviews are a two-way street! Prepare thoughtful questions about the company culture, team dynamics, and how your voice can be heard within the organisation. This shows your genuine interest and helps you assess if it’s the right fit for you.
