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- Tasks: Manage clinical research sites from start to finish, ensuring successful study execution.
- Company: Join a leading global CRO dedicated to advancing healthcare through innovative research.
- Benefits: Enjoy a competitive salary, car allowance, and the flexibility of remote work.
- Why this job: Be part of a mission-driven team that values transparency, support, and social impact.
- Qualifications: Bachelor's in a health-related field and at least 4 years of CRA experience required.
- Other info: RBW Consulting champions diversity and equal opportunities in the workplace.
The predicted salary is between 55000 - 60000 £ per year.
Location: Remote in UK
Salary: £55,000 - £60,000 plus car allowance or company car
Company: Global CRO
RBW Consulting are excited to announce an opportunity on behalf of one of our close clients. This company is 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.
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;
- 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 (, , United Kingdom) employer: RBW Consulting
Contact Detail:
RBW Consulting Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Principal Clinical Research Associate (, , United Kingdom)
✨Tip Number 1
Network with professionals in the clinical research field. Attend industry conferences or webinars to meet potential colleagues and learn about the latest trends. This can help you gain insights into what companies like ours are looking for in a Principal Clinical Research Associate.
✨Tip Number 2
Familiarise yourself with the specific therapeutic areas that the company focuses on. Understanding the nuances of these areas can give you an edge during interviews, as it shows your commitment and knowledge about the company's work.
✨Tip Number 3
Prepare for potential interview questions by reviewing common scenarios faced by Clinical Research Associates. Think about how you would handle site management challenges or patient recruitment issues, as these are key responsibilities of the role.
✨Tip Number 4
Showcase your soft skills during the interview process. As a Principal Clinical Research Associate, you'll need strong communication and leadership abilities. Be ready to discuss examples of how you've successfully managed teams or communicated complex information to stakeholders.
We think you need these skills to ace Principal Clinical Research Associate (, , United Kingdom)
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in clinical research, particularly your roles as a Clinical Research Associate. Emphasise your autonomy in managing investigator sites and any specific therapeutic areas you've worked in.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for clinical research and your understanding of the company's mission. Mention your proven CRA experience and how it aligns with the responsibilities outlined in the job description.
Highlight Relevant Qualifications: Clearly state your Bachelor of Science in a health-related field and any additional certifications or training that are pertinent to the role. This will help demonstrate your qualifications and commitment to the field.
Showcase Soft Skills: In your application, don't forget to mention soft skills such as communication, teamwork, and problem-solving. These are crucial in a role that involves coordinating with various stakeholders and managing site operations.
How to prepare for a job interview at RBW Consulting
✨Know Your Clinical Research Fundamentals
Make sure you have a solid understanding of clinical research methodologies and medical terminology. Brush up on your knowledge of phases 1 to 3 studies, as well as the specific responsibilities of a Principal Clinical Research Associate.
✨Demonstrate Autonomy and Leadership
Be prepared to discuss your experience managing investigator sites independently. Highlight instances where you've successfully navigated the study life cycle from start-up to close-out, showcasing your ability to lead and make decisions.
✨Prepare for Scenario-Based Questions
Expect questions that assess your problem-solving skills in real-world scenarios. Think about challenges you've faced in previous roles, particularly around patient recruitment, adverse event reporting, or regulatory compliance, and how you overcame them.
✨Showcase Your Communication Skills
As a Principal CRA, you'll need to communicate effectively with various stakeholders. Be ready to demonstrate your ability to coordinate meetings, present findings, and ensure clear communication regarding clinical supplies and safety issues.
