JOB DETAILS

GCP Consultant (GCP Auditor)

CompanyErgomed
LocationLisbon
Work ModeOn Site
PostedMarch 19, 2026
About The Company
PrimeVigilance, an Ergomed Group company, was established in 2008 by Dr. Miroslav Reljanovic together with co-founder Dr. Elliot Brown. PrimeVigilance offers holistic, top quality, cost-effective, innovative clinical safety and PV services for pharmaceutical, biotechnology and medical device companies. Our leaders have an unrivalled reputation in the sector with a network of SMEs across the world. These include former senior regulators and consultants with expansive industry experience.
About the Role

Company Description

ADAMAS is a well-established, leading provider of mission-critical regulatory compliance and consulting services to the global pharmaceutical industry. It operates across Good Clinical Practice (GCP), Good Pharmacovigilance Practice (GVP), Good Manufacturing Practice (GMP), Good Laboratory Practice (GLP) and Computer Systems Compliance (CSC) (together, GxP).  

Founded in 2007, ADAMAS has focused on ensuring that the highest standards of best practice are attained across the pharmaceutical sector. ADAMAS has an established client base with an expansive global reach, including North America, Europe, and Asia Pacific. We work with over 100 currently active clients and have worked with over 700 pharmaceutical companies, including 40 of the 50 largest global pharma and biotech companies. 

At ADAMAS, our people are our primary asset. We possess the highest and broadest level of in-house knowledge and can deliver genuine expertise and experience globally via in-house resources. ADAMAS's success is down to the calibre of its people – to reward them we offer a competitive salary with benefits, excellent working conditions and a fulfilling and rewarding career, with plenty of opportunities for further development.   

Job Description

  • Planning, preparation, conduct, reporting and follow up of various types of GCP audits according to expected quality and timelines  

  • Executing audits based on a comprehensive understanding of all regulatory requirements and Good Clinical Practice (GCP).  

  • Performing GCP quality assurance projects on behalf of client companies within the pharmaceutical/biotechnology industry.  

  • Assisting with business development activities  

Qualifications

  • BSc in Life Science preferred  

  • Experience in conducting and leading internal and external GCP audits for a variety of stakeholders  

  • Experience in conducting a range of service provider audits (e.g., full-service CRO, biostatistics, data management, phase I)  

  • Experience in conducting GCP systems audits.  

  • Experience in coordinating and managing inspection preparation activities for GCP process inspections both at the sponsor and investigator site.  

  • Experience in conducting GCP mock inspections to Competent Authority standard considered a significant advantage.  

  • Expert knowledge of national and international GCP legislation and guidelines  

  • Up to 40% travel and ability to conduct remote audits 

Additional Information

Why ADAMAS?     

As an organization, we prioritize diversity, equity, and inclusion by creating an equal opportunities workplace and a human-centric environment where people of all cultural backgrounds, genders and ages can contribute and grow.    

To succeed we must work together with a human first approach. Why? Because our people are our greatest strength leading to our continued success on improving the lives of those around us.   

We offer:  

  • Training and career development opportunities internally    

  • Strong emphasis on personal and professional growth   

  • Friendly, supportive working environment   

  • Opportunity to work with colleagues based all over the world, with English as the company language.   

Our core values are key to how we operate, and if you feel they resonate with you then ADAMAS, an Ergomed Company is a great place to join!    

Quality   

Integrity & Trust    

Drive & Passion    

Agility & Responsiveness    

Belonging   

Collaborative Partnerships    

We look forward to welcoming your application.  

  • Department: GCP Compliance
  • Key Skills
    GCP AuditsGCP Quality AssuranceRegulatory RequirementsLife ScienceInternal AuditsExternal AuditsService Provider AuditsGCP Systems AuditsInspection PreparationGCP Mock InspectionsGCP LegislationTravelRemote AuditsBusiness Development
    Categories
    ConsultingHealthcareScience & ResearchLegalTechnology
    Benefits
    Competitive salaryBenefitsExcellent working conditionsFulfilling and rewarding careerOpportunities for further development
    Job Information
    📋Core Responsibilities
    The role involves planning, preparation, conducting, reporting, and following up on various types of GCP audits according to quality standards and timelines. This includes executing audits based on a comprehensive understanding of GCP and regulatory requirements, as well as performing GCP quality assurance projects for pharmaceutical/biotechnology clients.
    📋Job Type
    full time
    📊Experience Level
    5-10
    💼Company Size
    1337
    📊Visa Sponsorship
    No
    💼Language
    English
    🏢Working Hours
    40 hours
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