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Research Scientist à Grande-Bretagne

Lead Clinical Research Associate

JR United Kingdom

Cardiff
Sur place
GBP 40 000 - 50 000
Il y a 30+ jours
Je veux recevoir les dernières offres d’emploi de Research Scientist

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GBP 45 000 - 60 000
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GBP 50 000 - 70 000
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JR United Kingdom

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GBP 80 000 - 100 000
Il y a 30+ jours
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JR United Kingdom

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Sur place
GBP 50 000 - 70 000
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GBP 50 000 - 70 000
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Lead Clinical Research Associate
JR United Kingdom
Cardiff
Sur place
GBP 40 000 - 50 000
Plein temps
Il y a 30+ jours

Résumé du poste

A Contract Research Organization is looking for a Lead Clinical Research Associate based in Cardiff with at least 5 years of CRA experience. The role involves managing investigator sites through the study lifecycle, conducting monitoring visits, and ensuring regulatory compliance. This position offers a supportive environment focused on professional growth and a competitive benefits package including a car allowance and bonuses.

Prestations

Car allowance
Bonus
Supportive management team
Career development opportunities

Qualifications

  • 5 years minimum CRA experience required.
  • Bachelor's degree or equivalent in a health-related field.
  • Proven track record in site management.

Responsabilités

  • Manage the successful operation of investigator sites throughout the study lifecycle.
  • Perform feasibility and closeout visits for research sites.
  • Coordinate timely delivery and storage of clinical supplies.

Connaissances

CRA experience
Health-related field knowledge
Regulatory compliance

Formation

Bachelor of Science in health-related field
Description du poste

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Lead Clinical Research Associate, cardiff

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Client:

RBW Consulting

Location:

cardiff, United Kingdom

Job Category:

Other

-

EU work permit required:

Yes

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Job Views:

1

Posted:

22.08.2025

Expiry Date:

06.10.2025

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Job Description:
  • Job Title: Lead Clinical Research Associate
  • Location: Remote in UK
  • Additional Benefits: Car allowance (or company car) and bonus
  • 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;
  • 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.

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.

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* Le salaire de référence se base sur les salaires cibles des leaders du marché dans leurs secteurs correspondants. Il vise à servir de guide pour aider les membres Premium à évaluer les postes vacants et contribuer aux négociations salariales. Le salaire de référence n’est pas fourni directement par l’entreprise et peut pourrait être beaucoup plus élevé ou plus bas.

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