Principal Clinical Research Associate

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

Job summary

A leading company in clinical research is seeking a Principal Clinical Research Associate to manage clinical trials across various therapeutic areas. The ideal candidate will have 4+ years of CRA experience and a Bachelor of Science in a health-related field, demonstrating expertise in medical terminology and clinical research methodologies in a remote UK-based role.

Benefits

Car allowance or company car

Supportive work culture with emphasis on growth

Qualifications

• Minimum of 4 years proven CRA experience.
• Broad knowledge of medical terminology and patient management in clinical settings.
• Basic understanding of drug therapy techniques.

Responsibilities

• Manage investigator sites independently throughout study lifecycle.
• Conduct site visits and prepare for investigator meetings.
• Assess patient recruitment and retention strategies.

Skills

Medical terminology

Patient management

Research methodologies

Education

Bachelor of Science in health-related field

Job description

Principal Clinical Research Associate, Southampton

Client: RBW Consulting

Location: Southampton, 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 excited to present an opportunity on behalf of a renowned CRO specializing in healthcare intelligence. They focus on unmet disease targets and advance clinical research by providing outsourced services to pharmaceutical and biotech companies.

Key accountabilities

• Manage investigator sites independently, overseeing the entire study lifecycle from start-up to close-out.
• Conduct feasibility, initiation, monitoring, and closeout visits for research sites across phases 1 to 3 and various therapeutic areas.
• Prepare for and attend investigator meetings, ensuring timely delivery and proper handling of clinical supplies, including drug safety follow-up.
• Verify source documents and review case report forms.
• Review regulatory documents.
• Report and follow up on adverse and serious adverse events.
• Assess patient recruitment and retention strategies.

Qualifications

• Bachelor of Science in a health-related field or equivalent.
• Minimum of 4 years proven CRA experience.
• Broad knowledge of medical terminology and patient management in clinical settings.
• Basic understanding of drug therapy techniques and research methodologies.

Application Process

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

About RBW Consulting

RBW Consulting is a life sciences talent and strategic consultancy committed to supporting healthcare innovation. We foster a culture of support, transparency, and mutual growth, valuing our people and their diverse backgrounds.

Equal Opportunity Statement

RBW Consulting is dedicated to diversity and inclusion, ensuring equal opportunities for all applicants regardless of race, ethnicity, gender, disability, or other protected characteristics.