Senior Clinical Research Associate

JR United Kingdom; Portsmouth; Remote; GBP 50,000 - 56,000; Full time

Job summary

A leading consultancy in the healthcare intelligence sector is seeking a Senior Clinical Research Associate to manage clinical investigations across various therapeutic areas. This role entails overseeing study lifecycles, ensuring regulatory compliance, and enhancing patient recruitment efforts. The ideal candidate has a BSc in a health-related field and at least 3 years of experience as a CRA.

Qualifications

• Bachelor's degree in a health-related field or equivalent.
• Minimum 3 years proven CRA experience.
• Broad knowledge of medical terminology and clinical patient management.

Responsibilities

• Manage investigator sites independently throughout the study lifecycle.
• Conduct feasibility, pre-study, initiation, monitoring, and closeout visits.
• Prepare for and attend investigator meetings and follow up on drug safety.

Skills

Medical terminology

Patient management

Drug therapy techniques

Clinical research methodologies

Education

Bachelor of Science in health-related field

Job description

Senior Clinical Research Associate, Portsmouth, Hampshire

Client:

RBW Consulting

Location:

Portsmouth, Hampshire, United Kingdom

Job Category:

Other

EU work permit required:

Yes

Job Views:

5

Posted:

04.06.2025

Expiry Date:

19.07.2025

Job Description:

• Job Title: Senior Clinical Research Associate
• Location: Remote in UK
• Salary: £50,000 - £56,000 plus car allowance or company car
• Company: Global CRO

RBW Consulting is excited to offer an opportunity with a renowned CRO specializing in healthcare intelligence and operating within a European culture. The company focuses on unmet disease target areas and advances clinical research by providing outsourced services to pharmaceutical and biotechnology companies.

Key accountabilities:

• Manage investigator sites independently throughout the study lifecycle (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, proper storage, and accountability of clinical supplies, and follow-up on drug safety issues;
• Perform source document verification and case report form review;
• Review regulatory documents;
• Report and follow-up on adverse and serious adverse events; and
• Assess patient recruitment and retention.

Qualifications:

• Bachelor of Science in a health-related field (or equivalent);
• Minimum of 3 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 committed to making a difference through Human Intelligence. We support life sciences companies in innovating and scaling to improve health outcomes. We foster a culture of support, transparency, and mutual commitment, valuing our people as our greatest asset.

Equal Opportunities Statement:

RBW Consulting is an equal opportunity employer. We prioritize talent and potential, challenge the status quo, and value diversity in our workforce. We do not discriminate based on race, ethnicity, gender, sexual orientation, religion, age, disability, or any other protected characteristic. We are dedicated to building a diverse team that reflects a variety of backgrounds, perspectives, and skills.