Clinical Research Associate II

Clinical Research Associate II

Plymouth Full-Time 36000 - 60000 £ / year (est.) Home office possible
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Precision Medicine Group

At a Glance

  • Tasks: Monitor clinical studies and ensure 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 cancer research while working from home in Northern Ireland.
  • Qualifications: 2+ years CRA experience; oncology knowledge is a plus.
  • Other info: Flexible travel commitments and a chance to influence meaningful change.

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.
We are hiring a CRA II, this position will be fully home based in Northern Ireland, monitoring sites in Ireland and across 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
Minimum Required:

  • 4-year college degree or equivalent experience

Other Required

  • 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.
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.
Any data provided as a part of this application will be stored in accordance with our Privacy Policy. For CA applicants, please also refer to our CA Privacy Notice.
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 at QuestionForHR@precisionmedicinegrp.com.
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 employer: Precision Medicine Group

At Precision for Medicine, we pride ourselves on being a supportive and engaging employer, particularly for our Clinical Research Associates. With a focus on work/life balance, a lower-than-average number of protocols, and a culture that values employee input, you will find a fulfilling environment where your contributions are recognised and appreciated. Based in Northern Ireland, this fully home-based role offers the unique opportunity to influence clinical studies across Ireland and the UK while enjoying reasonable travel commitments and a strong sense of community.
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

✨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 CRA II.

✨Tip Number 2

Prepare for your interviews by diving deep into the specifics of clinical research. Brush up on ICH-GCP guidelines and be ready to discuss how you've handled challenges in past roles. Show them you're not just a fit on paper but also in practice!

✨Tip Number 3

Don’t forget to showcase your soft skills! Being calm and responsive is key in this role. Share examples of how you've navigated conflicts or tricky situations in previous jobs to demonstrate your problem-solving abilities.

✨Tip Number 4

Apply through our website! It’s the best way to ensure your application gets seen by the right people. Plus, it shows you’re genuinely interested in joining our team at Precision for Medicine.

We think you need these skills to ace Clinical Research Associate II

Clinical Study Monitoring
Attention to Detail
Problem-Solving Skills
Risk Identification and Mitigation
Conflict Resolution
Regulatory Knowledge (SOPs, ICH-GCP)
Project Coordination
Communication Skills
Oncology Knowledge
Adaptability
Time Management
Team Collaboration
Home-Based Work Capability
Travel Availability

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 CRA. Focus on your oncology experience and any specific projects that showcase your skills in monitoring and managing clinical studies.

Be Detail-Oriented: We love candidates who pay attention to detail! Double-check your application for any typos or errors, and ensure that all your qualifications and experiences are clearly outlined. This reflects the meticulous nature we value in our work.

Apply Through Our Website: Don’t forget to apply through our website! It’s the best way to ensure your application gets into the right hands. Plus, it shows us that you’re serious about joining our team at Precision for Medicine.

How to prepare for a job interview at Precision Medicine Group

✨Know Your Protocols

As a Clinical Research Associate II, you'll need to be a protocol expert. Make sure you thoroughly understand the protocols relevant to the position and be ready to discuss how you've successfully managed similar studies in the past.

✨Showcase Your Problem-Solving Skills

Precision for Medicine values quick and creative solutions. Prepare examples of challenges you've faced in previous roles and how you overcame them. This will demonstrate your calm and thoughtful approach when things don’t go as planned.

✨Highlight Your Attention to Detail

With an impeccable eye for detail being crucial in this role, come prepared with specific instances where your attention to detail made a significant impact on a project. This will show that you take responsibility for the quality of your work.

✨Be Ready to Discuss Conflict Resolution

Handling conflict effectively is key in this position. Think of examples where you've used tried and true resolution strategies to manage conflicts in a team setting. This will illustrate your ability to maintain a positive work environment.

Clinical Research Associate II
Precision Medicine Group
Location: Plymouth
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