At a Glance
- Tasks: Lead the management of clinical research sites from start to finish.
- Company: Join a rapidly growing global CRO focused on innovative therapies.
- Benefits: Enjoy a competitive salary, car allowance, bonuses, and remote work flexibility.
- Other info: Work with cutting-edge technology and a culture that values diversity and inclusion.
- Why this job: Be part of a supportive team dedicated to your professional growth and impactful research.
- Qualifications: Bachelor's in a health-related field and at least 3 years of CRA experience required.
The predicted salary is between 48000 - 52000 £ per year.
- Job Title: Lead Clinical Research Associate
- Location: Remote in UK
- Salary: £56,000 – £63,000 (DOE)
- Additional Benefits: Car allowance (or company car) and bonus
- Sign-on Bonus: Potential sign-on bonus for qualified candidates
- Company: Global CRO
RBW Consulting is thrilled to present an exciting opportunity on behalf of one of our esteemed clients. As one of the few rapidly growing Contract Research Organizations (CROs) for UK studies, our client is expanding their site management team with multiple hires this year. They are involved in a diverse range of studies, including cutting-edge research in advanced therapies such as CAR-T.
Join a highly experienced team dedicated to excellence in clinical research. In this role, you will benefit from a supportive management team committed to your professional growth. They provide clear guidance on the skills needed for advancement and offer fluid career development opportunities across various departments.
This company prioritizes quality over metrics and is currently generating significant excitement within their UK team.
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; 5 years minimum
Why Join?
- Supportive Environment: Build strong relationships with a transparent management team focused on your development.
- Innovative Approach: Work with a company that embraces a 360 monitoring approach and leverages AI to enhance efficiency and save time.
- Results-Driven KPIs: Our client\’s key performance indicators are centered around tangible study outcomes, such as patient recruitment, visit reports, and resolving site issues.
- Administrative Support: Dedicated admin staff to help with site management tasks, helping to maintain a balanced workload.
- Training: Extensive training and buddy system in place.
- Career Growth: promotion opportunities up to 4 times a year.
- Therapy Areas: Access to mixed therapy areas, including advanced therapies like CAR-T.
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.
Lead Clinical Research Associate employer: RBW Consulting
Contact Detail:
RBW Consulting Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Lead Clinical Research Associate
✨Tip Number 1
Network with professionals in the clinical research field, especially those who work at CROs. Attend industry conferences or webinars to connect with potential colleagues and learn more about the company culture.
✨Tip Number 2
Familiarise yourself with the latest advancements in clinical research, particularly in advanced therapies like CAR-T. This knowledge will not only impress during interviews but also demonstrate your commitment to staying updated in the field.
✨Tip Number 3
Prepare for the interview by understanding the company's approach to site management and their emphasis on quality over metrics. Be ready to discuss how you can contribute to their results-driven KPIs.
✨Tip Number 4
Showcase your leadership skills and experience in managing investigator sites. Be prepared to provide examples of how you've successfully navigated challenges in previous roles, as this will align with the responsibilities of a Lead Clinical Research Associate.
We think you need these skills to ace Lead Clinical Research Associate
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in clinical research, particularly any roles where you've managed investigator sites or conducted monitoring visits. Use specific examples to demonstrate your skills and achievements.
Craft a Compelling Cover Letter: Write a cover letter that not only outlines your qualifications but also expresses your enthusiasm for the role. Mention your understanding of the company's innovative approach and how your background aligns with their values.
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. Emphasise your proven CRA experience, especially if you have over three years in the field.
Showcase Soft Skills: In addition to technical skills, highlight soft skills such as communication, teamwork, and problem-solving. These are crucial in a supportive environment like the one described in the job posting.
How to prepare for a job interview at RBW Consulting
✨Showcase Your Experience
Make sure to highlight your previous experience as a Clinical Research Associate, especially any specific projects or studies you've managed. Discuss the phases you've worked on and how you contributed to their success.
✨Understand the Company Culture
Research the company’s values and culture, particularly their focus on quality over metrics. Be prepared to discuss how your personal values align with theirs and how you can contribute to their supportive environment.
✨Prepare for Technical Questions
Expect questions related to regulatory document review, source document verification, and adverse event reporting. Brush up on these topics and be ready to provide examples from your past work.
✨Demonstrate Your Problem-Solving Skills
Be ready to discuss challenges you've faced in previous roles and how you overcame them. This will show your ability to handle site issues and patient recruitment effectively, which is crucial for this role.