Principal Clinical Research Associate

RBW Consulting; High Wycombe; Remote; GBP 55,000 - 60,000; Full time

Job summary

RBW Consulting is seeking a Principal Clinical Research Associate to manage clinical studies remotely in the UK. This role entails overseeing the entire study lifecycle, conducting site visits, and ensuring regulatory compliance while requiring a Bachelor of Science and proven CRA experience. Join a leading CRO focused on improving health outcomes through clinical research.

Qualifications

• Proven CRA experience with a minimum of 4 years.
• Broad knowledge of medical terminology and clinical patient management.
• Basic understanding of drug therapy techniques and clinical research methodologies.

Responsibilities

• Manage investigator sites independently throughout the study lifecycle.
• Conduct feasibility, pre-study, initiation, monitoring, and closeout visits.
• Report and follow-up on adverse and serious adverse events.

Skills

Medical terminology

Clinical patient management

Drug therapy techniques

Clinical research methodologies

Education

Bachelor of Science in a health-related field

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 one of our esteemed clients. This company is a renowned CRO with a focus on healthcare intelligence and a European culture. They address unmet disease targets and advance clinical research by providing outsourced services to pharmaceutical and biotechnology companies.

Key Accountabilities

1. Manage investigator sites independently, overseeing the entire study lifecycle (start-up to close-out).
2. Conduct feasibility, pre-study, initiation, monitoring, and closeout visits for research sites, mainly phase 1 to 3, across all therapeutic areas.
3. Prepare for and attend investigator meetings, ensuring timely delivery and proper storage and accountability of clinical supplies, along with follow-up on drug safety issues.
4. Perform source document verification and review case report forms.
5. Review regulatory documents.
6. Conduct study drug inventory management.
7. Report and follow-up on adverse and serious adverse events.
8. Assess patient recruitment and retention strategies.

Qualifications

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

Application Process

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 worldwide. We foster a culture of support, transparency, and mutual commitment, investing in our people and values over short-term gains.

RBW Consulting is an equal opportunity employer and agency. We value diversity and are dedicated to creating an inclusive environment that reflects a variety of backgrounds, perspectives, and skills.