JOB DETAILS

CRA II / Senior Clinical Research Associate (French speaking)

CompanyErgomed
LocationGuildford
Work ModeOn Site
PostedAugust 5, 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

Medicine moves forward here. So will you.

 

Ergomed is a specialist clinical research organization focused on rare disease and select oncology indications. We focus on the most complex trials, the studies where experience, judgement, and rigorous operational accountability make the biggest difference. We partner with small to midsize biotech companies to move promising therapies through early phase development, so they reach the patients sooner.

 

We choose complex work on purpose. Rare disease and oncology trials carry real operational risk, and our people are experts at reducing it, protecting timelines, data quality and the experience of sites and patients at the same time. It is demanding, meaningful work, and no one here forgets that patients cannot wait.

 

That is why culture matters to us as much as capability. We have built a collaborative, international team where people share ideas, grow their careers and are trusted to take ownership early. With colleagues across North America, South America, Europe, Asia and Australia, we value teamwork, flexibility and a real commitment to work-life balance, because good science comes from people who feel supported.

 

If you want work with purpose, the agility to make an impact and a team that cares about the people behind the work as much as the work itself, we would love to hear from you.

Job Description

  • National Travel Required as well as travel to France and Belgium (French-speaking part)
  • Performs on-site or remote Pre-Study, Initiation, Interim, and Close-Out monitoring visit activities to ensure that facilities and staff at the investigational site continue to be adequate for the conduct of the study
  • Identifies the investigators and verifies that the investigator has adequate qualifications, resources, facilities, equipment and staff to conducting the clinical study throughout the study period.
  • Trains investigational site staff as necessary
  • When applicable, supports preparation of regulatory and / or EC submissions

Qualifications

  • College/University degree in Life Sciences or an equivalent combination of education, training & experience
  • Extensive on-site monitoring experience in phase 2/3 trials, ideally with experience of complex trials such as oncology / rare dieses 
  • Full working proficiency in English and French
  • Ability to plan, multitask and work in a dynamic team environment
  • Communication, collaboration, and problem-solving skills
  • Ability to travel

Additional Information

When you join Ergomed Group, you make a difference by helping to bring safe and effective pharmaceutical treatment to patients around the world. You’ll join a passionate and collaborative team of experts in clinical research, pharmacovigilance, and quality consulting.

 

We are diverse in many ways, yet our values unite us. Our values are how we work, not words on a wall. If they sound like you, you will feel at home here.

 

  • Quality: we hold ourselves to the standard patients deserve.
  • Integrity and trust: we do the right thing, especially when it is hard.
  • Drive and passion: we care about the outcome, because someone is waiting on it.
  • Agility and responsiveness: we move quickly, because patients cannot wait.
  • Belonging: everyone is welcome, and every voice counts.
  • Collaborative partnerships: we go further by going together.

 

We look forward to welcoming your application.

 

 

  • Department: Clinical Monitoring
  • Key Skills
    Clinical monitoringOncologyRare diseasePhase 2/3 trialsRegulatory submissionsSite initiationData qualityFrench languageEnglish languageCommunicationCollaborationProblem-solvingMultitaskingClinical researchPharmacovigilance
    Categories
    HealthcareScience & ResearchConsulting
    Job Information
    📋Core Responsibilities
    Perform on-site and remote monitoring visits including pre-study, initiation, interim, and close-out activities to ensure site compliance. Identify and verify investigator qualifications and provide necessary training to site staff throughout the study period.
    📋Job Type
    full time
    📊Experience Level
    5-10
    💼Company Size
    1384
    📊Visa Sponsorship
    No
    💼Language
    English
    🏢Working Hours
    40 hours
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