Senior Clinical Research Associate

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

Job summary

A leading CRO seeks a Senior Clinical Research Associate to manage investigator sites throughout the study lifecycle, ensuring compliance with regulatory standards. This role requires strong clinical knowledge and at least 3 years of relevant experience. The successful candidate will engage in phases 1 to 3 across therapeutic areas, with a focus on improving health outcomes.

Qualifications

• At least 3 years of proven Clinical Research Associate experience required.
• Familiarity with clinical standards and regulatory guidelines.
• Competence in source data verification and regulatory document review.

Responsibilities

• Manage investigator sites from start-up to close-out.
• Conduct feasibility, initiation, monitoring, and closeout visits.
• Report adverse events and assess patient recruitment and retention.

Skills

Knowledge of medical terminology

Clinical patient management

Understanding of drug therapy techniques

Research methodologies

Education

Bachelor of Science in a health-related field

Job description

Senior Clinical Research Associate, Shrewsbury

Client:

RBW Consulting

Location:

Shrewsbury, United Kingdom

Job Category:

Other

EU work permit required:

Yes

Job Views:

4

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 seeking a Senior Clinical Research Associate for a renowned CRO with a European culture, specializing in healthcare intelligence. The role involves managing investigator sites throughout the study lifecycle, conducting various site visits, preparing for meetings, managing clinical supplies, and ensuring compliance with safety and regulatory standards. The position covers phases 1 to 3 across therapeutic areas.

Key responsibilities include:

• Managing investigator sites from start-up to close-out;
• Conducting feasibility, initiation, monitoring, and closeout visits;
• Attending investigator meetings and managing clinical supplies;
• Performing source data verification and regulatory document review;
• Reporting adverse events and assessing patient recruitment and retention.

Qualifications:

• Bachelor of Science in a health-related field or equivalent;
• Minimum 3 years of proven CRA experience;
• Knowledge of medical terminology and clinical patient management;
• Basic understanding of drug therapy techniques and research methodologies.

To apply:

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

About RBW Consulting:

RBW Consulting is a life sciences talent and consultancy firm committed to supporting health innovations and fostering a diverse, inclusive workplace. We value talent, transparency, and mutual support, aiming to improve health outcomes globally.

Equal Opportunity Statement:

We are an equal opportunities employer, valuing diversity and inclusivity at all levels of our organization.