Principal Clinical Research Associate

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

Job summary

A leading company in healthcare intelligence is seeking a Principal Clinical Research Associate based in the Oxford District. The successful candidate will manage clinical study sites and ensure the proper conduct of clinical research. Candidates must hold a Bachelor's degree in a health-related field and have a minimum of 4 years of experience as a Clinical Research Associate. The role offers a competitive salary, with further benefits including a car allowance.

Qualifications

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

Responsibilities

• Manage investigator sites independently across various therapeutic areas.
• Conduct feasibility and monitoring visits for research sites.
• Verify source documents and review case report forms.

Skills

Medical terminology

Clinical patient management

Patient recruitment strategies

Education

Bachelor of Science in a health-related field

Job description

Principal Clinical Research Associate, Oxford District

Client: RBW Consulting

Location: Oxford district, 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 with a renowned CRO specializing in healthcare intelligence and operating across Europe. They focus on unmet disease targets and advancing 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, pre-study, initiation, monitoring, and closeout visits for research sites, mainly phase 1 to 3 across various therapeutic areas.
• Prepare for and attend investigator meetings, ensuring timely delivery and proper storage of clinical supplies, and follow-up on drug safety issues.
• Verify source documents and review case report forms.
• Review regulatory documents.
• Report and follow-up on adverse and serious adverse events.
• Evaluate 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 clinical patient management.
• Basic understanding of drug therapy techniques and clinical research methodologies.

To apply:

Please click ‘apply’ or contact Joe Pearce for further information.

About RBW Consulting:

RBW Consulting is a life sciences talent and strategic consultancy driven by Human Intelligence. We support life sciences companies in innovation and scaling by providing talent, insights, and networks. Our mission is to improve health and wellbeing outcomes for patients, and we actively participate in initiatives that make a difference. We foster a culture of support, transparency, and mutual commitment, valuing and investing in our people.

Equality Statement: RBW Consulting is an equal opportunity employer. We prioritize talent and potential, challenge the status quo, and value diversity in backgrounds, perspectives, and skills. We do not discriminate based on race, ethnicity, gender, sexual orientation, religion, age, disability, or other protected statuses.