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Precision Medicine Group

GCP Auditor

Remote, United Kingdom
Posted about 14 hours ago
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Precision for Medicine

Precision for Medicine is a global Clinical Research Organisation. Precision’s uniquely integrated offering enables the science of precision medicine by combining novel clinical trial designs, industry-leading operational and medical experts, advanced biomarker and data analytics solutions, and an unequivocal real passion for rare diseases and oncology, in addition to working across other therapeutic areas.

As our company continues to grow, we are seeking a full-time GCP Auditor to join our team. This position is offered fully remote.

About the Role

As a GCP Auditor, you will support the audit program and clinical projects to ensure compliance with applicable regulations and Precision procedures. You will be responsible for providing oversight and subject matter expertise to quality and compliance activities, supporting project teams during all stages of a clinical study.

Essential Functions

  • Support the Quality Management System including SOPs, training, and CAPA
  • Process and maintain documentation for controlled documents, as required
  • Develop and administer training for employees and/or consultants
  • Host client/sponsor audits and support regulatory inspections
  • Coordinate and conduct assessments of potential and contracted vendors, including vendor audits as warranted
  • Coordinate and conduct internal audits of quality systems
  • Coordinate and conduct investigator site audits
  • Coordinate and conduct trial master file audits
  • Participate on computer systems validation projects and systems change control process
  • Provide QA consultation and support to assigned project teams internally and externally
  • Support and manage reported quality issues and any associated corrective and preventive actions
  • Monitor quality systems to provide feedback on compliance risks to QA management and identify opportunities for improvement
  • Maintains Q&C trackers, databases, metrics, and files
  • Follow applicable regulations and standards, including but not limited to local regulations (US FDA and EU), ICH, and company policies and procedures

Reasons to use Rodeo

I’m in my final year doing Economics and I don’t know whether to apply for grad schemes now or do a masters first. What do you think?

Honest answer — it depends on where you want to end up. A lot of top grad schemes (Big 4, civil service, banking) don’t need a masters. Let’s look at the ones you’d be competitive for now, and we can decide if a masters actually adds anything.

Also worth knowing: most autumn 2026 applications are open now. Timing matters more than you think.

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Grad scheme, placement, apprenticeship? Not sure what you want yet — that's fine. Your agent talks it through with you and turns "I have no idea" into a shortlist.

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Graduate Consultant — 2026 Scheme

PwC·London, UK
£35,000/yr

Why you're a good match

Strong

Your economics background and your summer at a regional bank line up with what PwC looks for on the consulting scheme. Applications close in four weeks.

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It searches the market for you

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Why you're a good match

You’ve got the grades and the economics background, and your bank internship is exactly the experience this scheme looks for. Apply soon — deadlines close within the month.

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Strong

Experience fit

Your summer at the bank plus your econometrics coursework map directly to the day-one responsibilities on this scheme — client modelling, market briefings, and deal support.

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Only hits

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Who We Are Seeking

The ideal candidate will have:

  • Extensive, working knowledge of managing audits in Clinical Trials environment: routine GCP audits, CRO process audits, Vendor Audits
  • Working knowledge of GCP/ICH guidelines and FDA regulations and standards
  • Bachelor’s degree in a science, healthcare, or related field of study; combination of qualifications and equivalent relevant experience may be accepted as an alternative
  • Availability to travel up to 25% domestically and/or internationally

Preferred

  • 2 or more years’ experience in QA GCP department in a related industry
  • QA certification preferred (e.g., CQA, SQA, etc.)
  • Experience with electronic clinical trial systems (e.g., EDC, CTMS, IxRS, ePRO, etc.)

#LI-OS1 #LI-Remote

About Us

We invite you to learn more about our growing organization serving our clients that are researching groundbreaking cancer therapies. We strive to ensure employees feel appreciated for the contributions they make every single day. You will provide input and have your ideas valued and nurtured, impacting positive change for the company.

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Privacy Notice

Any data provided as a part of this application will be stored in accordance with our Privacy Policy. For CA applicants, please also refer to our CA Privacy Notice.

Equal Opportunity Employer

Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or other characteristics protected by law.

Accommodation

If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at myHR@precisionmedicinegrp.com.

Recruitment Fraud Warning

Please be aware that fraudulent individuals and websites may impersonate Precision Medicine Group or its affiliates and attempt to obtain personal, financial, or banking information through fake job postings or employment offers. Precision Medicine Group will never request payment, banking details, or other sensitive financial information as part of the recruitment process. If you believe you have been targeted by a recruitment scam, we encourage you to report the incident to your local law enforcement authorities, consumer protection agency, or relevant cybercrime reporting organization in your country. Please also notify us at myHR@precisionmedicinegrp.com so we can investigate and take appropriate action.

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Skills

GCP Auditing
Quality Management Systems
CAPA Process
Vendor Audits
Internal Audits
Investigator Site Audits
Trial Master File Audits
Computer Systems Validation
Regulatory Compliance
ICH Guidelines
FDA Regulations
EDC
CTMS
IxRS
ePRO

Location

United Kingdom

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