Principal Clinical Research Associate

JR United Kingdom; Lincoln; Remote; GBP 55,000 - 60,000; Full time

Job summary

A leading global CRO is seeking a Principal Clinical Research Associate to manage clinical trials from initiation to completion. This remote role requires a BSc in a health-related field and 4 years of CRA experience, emphasizing patient recruitment and safety oversight.

Qualifications

• Minimum 4 years proven CRA experience.
• Basic understanding of drug therapy techniques and clinical research methodologies.

Responsibilities

• Managing investigator sites throughout the study lifecycle from start-up to close-out.
• Conducting monitoring and closeout visits for phases 1 to 3 across therapeutic areas.
• Performing source document verification and case report form review.

Skills

Knowledge of medical terminology

Clinical patient management

Drug therapy techniques

Clinical research methodologies

Education

BSc in a health-related field

Job description

Principal Clinical Research Associate, Lincoln

Client:

RBW Consulting

Location:

Lincoln, United Kingdom

Job Category:

Other

EU work permit required:

Yes

Job Views:

3

Posted:

04.06.2025

Expiry Date:

19.07.2025

Job Description:

• Job Title: Principal Clinical Research Associate
• Location: Remote in UK
• Salary: £55,000 - £60,000 plus car allowance or company car
• Company: Global CRO

RBW Consulting is seeking a Principal Clinical Research Associate for a remote role in the UK. The company is a global CRO specializing in healthcare intelligence, focusing on unmet disease targets and advancing clinical research by providing outsourced services to pharmaceutical and biotechnology companies.

Key responsibilities include:

• Managing investigator sites throughout the study lifecycle (start-up to close-out);
• Conducting feasibility, initiation, monitoring, and closeout visits, mainly for phases 1 to 3 across various therapeutic areas;
• Preparing for and attending investigator meetings, overseeing clinical supplies, and addressing drug safety issues;
• Performing source document verification and case report form review;
• Reviewing regulatory documents;
• Reporting and following up on adverse and serious adverse events;
• Assessing patient recruitment and retention.

Qualifications:

• BSc in a health-related field or equivalent;
• Minimum 4 years proven CRA experience;
• Knowledge of medical terminology and clinical patient management;
• Basic understanding of drug therapy techniques and clinical research methodologies.

To apply:

Click ‘apply’ or contact Joe Pearce for further information.

About RBW Consulting:

RBW Consulting is a life sciences talent and strategic consultancy dedicated to supporting healthcare innovation. They emphasize a culture of support, transparency, and mutual growth, and are committed to diversity and equal opportunity in their recruitment practices.