Enable job alerts via email!

Principal Clinical Research Associate

JR United Kingdom

Bath

Remote

GBP 55,000 - 60,000

Full time

Yesterday
Be an early applicant

Boost your interview chances

Create a job specific, tailored resume for higher success rate.

Job summary

A leading company is looking for a Principal Clinical Research Associate based in Bath, UK. The role involves managing clinical sites through their lifecycle, conducting vital visits, and ensuring compliance with regulatory standards. Candidates should have a relevant Bachelor's degree and a minimum of four years of clinical research associate experience.

Qualifications

  • Bachelor of Science (or equivalent) required.
  • Proven CRA experience of at least 4 years.
  • Broad knowledge of medical and clinical research concepts.

Responsibilities

  • Manage investigator sites through the study life cycle.
  • Conduct feasibility, monitoring, and closeout visits.
  • Prepare for investigator meetings and manage clinical supplies.

Skills

Medical terminology
Clinical patient management
Drug therapy techniques
Clinical research methodologies

Education

Bachelor of Science in health-related field

Job description

Social network you want to login/join with:

Principal Clinical Research Associate, bath

col-narrow-left

Client:

RBW Consulting

Location:

bath, United Kingdom

Job Category:

Other

-

EU work permit required:

Yes

col-narrow-right

Job Views:

3

Posted:

04.06.2025

Expiry Date:

19.07.2025

col-wide

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 are excited to announce an opportunity on behalf of one of our close clients. This company are a renowned CRO with leading healthcare intelligence and a European culture. They treat unmet disease target areas and advance clinical research by providing outsourced services to pharmaceutical and biotechnology companies.

Key accountabilities

  • Autonomy of investigator sites with full responsibility for the successful management of sites through study life cycle (start-up to close-out);
  • Conduct feasibility, pre-study, initiation, monitoring, and closeout visits for research sites, mainly phase 1 to 3 and within all available therapeutic areas;
  • Prepare accordingly and attend investigator meetings, coordinating timely delivery and subsequent proper storage and accountability of clinical supplies and following-up of drug safety issues;
  • Perform source document verification and case report form review;
  • Perform regulatory document review;
  • Perform adverse event and serious adverse event reporting and follow-up; and
  • Assess patient recruitment and retention.

Qualifications

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

To apply:

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

About RBW Consulting

RBW Consulting is a life sciences talent & strategic consultancy with purpose, delivered through what we call Human Intelligence. We help life sciences businesses change the world by giving them the people, insight & networks to innovate and scale. We are proud of our role in helping companies deliver better health and wellbeing outcomes for patients We give back by playing an active role in funding initiatives that change lives We’ve created a culture rooted in support, transparency and mutual commitment. We lead with our values from the inside; empowering and investing in our people is more important than short-term commercial gain.

We are an equal opportunities Recruitment Business and Agency

RBW Consulting is an equal opportunity workplace. We prioritize talent (both current and potential) over resumes, challenge the status quo, and value people as our most important asset. We do not discriminate on the basis of race, ethnicity, colour, sex, gender identity or expression, sexual orientation, religion, age, marital status, visible or invisible disability, medical condition, national origin, veteran status, or any other protected status. We strive to be a diverse workforce that is representative at all levels and are committed to building a team that represents a variety of backgrounds, perspectives, and skills.

Get your free, confidential resume review.
or drag and drop a PDF, DOC, DOCX, ODT, or PAGES file up to 5MB.

Similar jobs

Principal Clinical Research Associate

JR United Kingdom

Southampton

Remote

GBP 55,000 - 60,000

Today
Be an early applicant

Principal Clinical Research Associate

JR United Kingdom

Bournemouth

Remote

GBP 55,000 - 60,000

Today
Be an early applicant

Principal Clinical Research Associate

JR United Kingdom

Gloucester

Remote

GBP 55,000 - 60,000

Today
Be an early applicant

Principal Clinical Research Associate

JR United Kingdom

Cheltenham

Remote

GBP 55,000 - 60,000

Today
Be an early applicant

Principal Clinical Research Associate

JR United Kingdom

Cardiff

Remote

GBP 55,000 - 60,000

Today
Be an early applicant

Principal Clinical Research Associate

JR United Kingdom

Worcester

Remote

GBP 55,000 - 60,000

Today
Be an early applicant

Principal Clinical Research Associate

JR United Kingdom

Lincoln

Remote

GBP 55,000 - 60,000

Today
Be an early applicant

Principal Clinical Research Associate

JR United Kingdom

London

Remote

GBP 55,000 - 60,000

Today
Be an early applicant

Principal Clinical Research Associate

JR United Kingdom

Stevenage

Remote

GBP 55,000 - 60,000

Today
Be an early applicant