GCP AUDITOR - LIFE SCIENCES

CPL and TAYLOR by Synergos srl; Birmingham; On-site; GBP 60,000; Full time

Job summary

A multinational consulting firm is seeking a GCP Auditor in Birmingham, UK. This full-time role involves independently reviewing clinical research activities, organizing GCP audits, and ensuring regulatory compliance. Candidates should have at least 5 years of GCP auditing experience and a degree in scientific disciplines. The position offers flexible hybrid working arrangements and a gross annual salary around £60,000, depending on experience. Join a collaborative, multicultural team and contribute to high-impact projects.

Benefits

Flexible working arrangements

Career growth opportunities

Continuous professional training

Qualifications

• At least 5 years of experience as a GCP Auditor or Consultant.
• Strong knowledge of GCP regulations and auditor qualification.
• Familiarity with the 2011 Legislative Decree on CROs.

Responsibilities

• Independently review clinical research activities.
• Schedule and document audits focusing on study sites.
• Produce comprehensive audit documentation.

Skills

GCP Auditor experience

Scientific degree

Knowledge of GCP regulations

International environments experience

Willingness to travel

Education

Degree in scientific disciplines

Job description

CPL & TAYLOR by Synergos is looking for:

GCP AUDITOR - LIFE SCIENCES

(Rif. ANN411296)

LOCATION: UK - possibility of full remote or hybrid work, with travel required

CONTRACT: Permanent, full-time

SALARY: Gross annual package around £60.000

The Company

An important international organization specializing in consulting and digital solutions for the Life Sciences sector, with headquarters in Italy. Established in 2010, it supports pharmaceutical and biotech companies in regulatory affairs, pharmacovigilance, clinical trials, medical affairs, and quality assurance. The company provides innovative digital tools and high value‑added services, with a strong focus on regulatory compliance and operational efficiency.

The Role

As a GCP Auditor, you will be responsible for independently reviewing clinical research activities conducted worldwide. You will schedule, carry out, and document around two audits each month, focusing on study sites, third‑party providers, and internal processes.

Main Responsibilities

• Organize, coordinate, and execute GCP audits, including site, vendor, system, and internal process evaluations
• Produce comprehensive audit documentation and clearly present observations and conclusions to clients
• Provide guidance on drafting and implementing CAPAs, ensuring actions are tracked and resolved within expected timelines
• Contribute to inspection‑preparedness activities and deliver client training when required
• Maintain up‑to‑date knowledge of international GCP standards and evolving regulatory expectations

Requirements

• At least 5 years of experience as a GCP Auditor or Consultant
• Degree in scientific disciplines
• Strong knowledge of GCP regulations and auditor qualification
• Familiarity with the 2011 Legislative Decree on CROs
• Experience in international environments and willingness to travel
• Knowledge of Computer System Validation is considered a plus

The Company Offers

• Full‑time, permanent employment contract
• Gross annual salary around £60.000, depending on experience
• Flexible working arrangements (remote or hybrid options)
• Inclusion in a collaborative and multicultural team
• Career growth opportunities and high‑impact projects
• Continuous professional training

All job postings are open to applicants of all genders (L.903/77).

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CPL & Taylor By Synergos Srl

Ricerca e Selezione del Personale - Aut. MLSPS Prot.13/I/0008775

Mantova - Parma - Verona - Modena - Brescia - Cremona

Main Office: [phone]

• Location: Birmingham, West Midlands
• Contract: Tempo indeterminato
• Salary: ₠ Gross annual package around £60.000/ Mese
• Commitment: Full time