Principal Clinical Research Associate
Principal Clinical Research Associate

Principal Clinical Research Associate

Wales Full-Time 60000 - 65000 £ / year (est.) No home office possible
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At a Glance

  • Tasks: Manage clinical research sites from start to finish, ensuring successful study execution.
  • Company: Join a leading CRO focused on innovative healthcare solutions and patient outcomes.
  • Benefits: Enjoy remote work, regional travel, and multiple promotion opportunities each year.
  • Why this job: Work on cutting-edge CAR-T and Gene Therapy studies in a supportive, values-driven culture.
  • Qualifications: Bachelor's in health-related field and at least 4 years of CRA experience required.
  • Other info: RBW Consulting values diversity and prioritizes talent over resumes.

The predicted salary is between 60000 - 65000 £ per year.

  • Job Title: Principal Clinical Research Associate
  • Location: Remote with regional travel
  • Salary: £60,000 – £65,000 plus £6000 car allowance
  • Company: Global CRO

RBW Consulting are excited to announce an opportunity on behalf of one of our close clients. This company are a renowned CRO with leading healthcare intelligence and a European culture. They treat unmet disease target areas and advance clinical research by providing outsourced services to pharmaceutical and biotechnology companies.

Here, you can travel regionally, earn increased reduced travel in the position, and have up to 4 promotion & salary increase opportunities throughout the year. Not only this but you can work on interesting CAR-T and Gene Therapy studies.

Key accountabilities

  • Autonomy of investigator sites with full responsibility for the successful management of sites through study life cycle (start-up to close-out);
  • Conduct feasibility, pre-study, initiation, monitoring, and closeout visits for research sites, mainly phase 1 to 3 and within all available therapeutic areas;
  • Prepare accordingly and attend investigator meetings, coordinating timely delivery and subsequent proper storage and accountability of clinical supplies and following-up of drug safety issues;
  • Perform source document verification and case report form review;
  • Perform regulatory document review;
  • Conduct study drug inventory;
  • Perform adverse event and serious adverse event reporting and follow-up; and
  • Assess patient recruitment and retention.

Qualifications

  • Bachelor of Science in health-related field (or equivalent)
  • Proven CRA experience; 4 years minimum
  • Broad knowledge of medical terminology and clinical patient management
  • Basic knowledge of drug therapy techniques and clinical research methodologies

To apply:

Please click ‘apply’ or contact Joe Pearce for any further information

About RBW Consulting

RBW Consulting is a life sciences talent & strategic consultancy with purpose, delivered through what we call Human Intelligence. We help life sciences businesses change the world by giving them the people, insight & networks to innovate and scale. We are proud of our role in helping companies deliver better health and wellbeing outcomes for patients We give back by playing an active role in funding initiatives that change lives We’ve created a culture rooted in support, transparency and mutual commitment. We lead with our values from the inside; empowering and investing in our people is more important than short-term commercial gain.

We are an equal opportunities Recruitment Business and Agency

RBW Consulting is an equal opportunity workplace. We prioritize talent (both current and potential) over resumes, challenge the status quo, and value people as our most important asset. We do not discriminate on the basis of race, ethnicity, colour, sex, gender identity or expression, sexual orientation, religion, age, marital status, visible or invisible disability, medical condition, national origin, veteran status, or any other protected status. We strive to be a diverse workforce that is representative at all levels and are committed to building a team that represents a variety of backgrounds, perspectives, and skills.

Principal Clinical Research Associate employer: RBW Consulting

RBW Consulting is an exceptional employer that fosters a culture of support, transparency, and mutual commitment, making it an ideal place for a Principal Clinical Research Associate. With opportunities for regional travel, competitive salary packages, and up to four promotion and salary increase opportunities each year, employees can expect meaningful career growth while working on cutting-edge CAR-T and Gene Therapy studies. The company values diversity and prioritizes talent, ensuring a rewarding and inclusive work environment.
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Contact Detail:

RBW Consulting Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Principal Clinical Research Associate

✨Tip Number 1

Familiarize yourself with the latest trends in CAR-T and Gene Therapy studies. This knowledge will not only help you stand out during discussions but also demonstrate your genuine interest in the field.

✨Tip Number 2

Network with professionals in the clinical research field, especially those who have experience as Clinical Research Associates. Engaging in conversations can provide valuable insights and potentially lead to referrals.

✨Tip Number 3

Prepare for potential interviews by practicing common CRA scenarios, such as site management challenges or patient recruitment strategies. Being able to discuss these topics confidently will showcase your expertise.

✨Tip Number 4

Research RBW Consulting's values and culture. Understanding their commitment to diversity and employee empowerment can help you align your responses during interviews and show that you're a good fit for their team.

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

Clinical Research Experience
Site Management
Feasibility Assessment
Monitoring Skills
Regulatory Knowledge
Adverse Event Reporting
Source Document Verification
Case Report Form Review
Patient Recruitment Strategies
Drug Safety Issue Follow-up
Knowledge of CAR-T and Gene Therapy
Communication Skills
Attention to Detail
Problem-Solving Skills
Team Collaboration

Some tips for your application 🫡

Understand the Role: Make sure to thoroughly read the job description for the Principal Clinical Research Associate position. Understand the key responsibilities and qualifications required, as this will help you tailor your application.

Highlight Relevant Experience: In your CV and cover letter, emphasize your proven CRA experience and any specific projects related to CAR-T and Gene Therapy studies. Use concrete examples to demonstrate your skills in managing investigator sites and conducting clinical research.

Showcase Your Qualifications: Clearly state your Bachelor of Science in a health-related field and any additional certifications or training relevant to clinical research. This will help establish your credibility and fit for the role.

Personalize Your Application: Address your cover letter to the hiring manager, if possible, and express your enthusiasm for the opportunity to work with RBW Consulting. Mention how your values align with their commitment to diversity and support within the workplace.

How to prepare for a job interview at RBW Consulting

✨Showcase Your CRA Experience

Make sure to highlight your previous experience as a Clinical Research Associate. Discuss specific projects you've worked on, especially those involving phase 1 to 3 studies, and how you managed the study life cycle from start-up to close-out.

✨Demonstrate Knowledge of Medical Terminology

Since the role requires a broad knowledge of medical terminology, be prepared to discuss relevant terms and concepts. This will show that you are well-versed in the language of clinical research and can communicate effectively with investigators and other stakeholders.

✨Prepare for Regulatory Questions

Expect questions related to regulatory document review and drug safety issues. Familiarize yourself with the regulations governing clinical trials and be ready to discuss how you ensure compliance in your work.

✨Discuss Patient Recruitment Strategies

Given the importance of patient recruitment and retention in clinical trials, be prepared to share your strategies for assessing and improving these areas. Highlight any successful initiatives you've implemented in past roles.

Principal Clinical Research Associate
RBW Consulting
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  • Principal Clinical Research Associate

    Wales
    Full-Time
    60000 - 65000 £ / year (est.)

    Application deadline: 2027-01-28

  • R

    RBW Consulting

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