Field Clinical Research Associate, French Speaking

NAMSA

Field Clinical Research Associate with NAMSA ensuring GCP compliance and site monitoring. Responsible for managing clinical site visits and communications across multiple studies.

Posted 7/29/2026full-timeRemote • 🇬🇧 United KingdomJuniorMid-LevelWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in clinical trial monitoring, ensuring compliance with Good Clinical Practice (GCP) and applicable regulations. Proficient in managing study documents, site communications, and metrics tracking while maintaining high standards of quality and organization.

Highest-signal resume keywords

Clinical Trial MonitoringGood Clinical Practice (GCP)Fluency in FrenchStudy Document ManagementOrganizational Skills

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Research ProcessesSite MonitoringQuality Control ReviewStudy Metrics TrackingSite QualificationSite InitiationSite Close-Out MonitoringAdverse Event TrackingStudy Start-Up ActivitiesNarrative Writing

Soft Skills

Verbal CommunicationWritten CommunicationIndependenceCollaboration

Tools & Technologies

Trial Master FileStudy DocumentsQuality Review Systems

Certifications & Qualifications

Society of Clinical Research Associates (SoCRA)Association of Clinical Research Professionals (ACRP)

Industry Keywords

Human Subject ProtectionRegulatory GuidelinesClinical Site MonitoringMedical Device ExperienceStudy Enrollment

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Works on assigned studies to ensure that human subject protection is maintained, Good Clinical Practice (GCP), and applicable regulations are followed.
Coordinates and manages clinical site monitoring responsibilities for assigned studies in accordance with contractual agreements, SOPs, and applicable regulatory guidelines.
May conduct on-site and remote site qualification, site initiation, interim, and site close-out monitoring visits.
Serve as primary point of contact for site questions relating to study enrollment, conduct, and close-out issues: liaise with appropriate study team members as needed.
Communicates through verbal and written communication with site investigator and project team overall site performance, trends, deficiencies, and concerns.
Supports study start-up activities such as tracking and performing quality review of study documents, completing, and distributing site activation letters, etc.
Performs study-related training.
Manages the development and maintenance of study documents, processes and systems as assigned.
Ensures quality and completeness of central and site master files. Tracks and maintains required study documents, performs quality control review, manages renewals.
Tracks study site and overall study metrics including but not limited to enrollment, deviations, adverse events, trial master file maintenance.
Attends internal and external meetings as required.
Provides all job-related progress reports and visit documentation as required.
May support safety activities such as narrative writing, managing the CEC/DSMB, etc.
OUS: Prepares and coordinates submissions to regulatory authorities.
May perform other activities as assigned.

Requirements

What you’ll need

Must be fluent in French residing in one of the locations noted above preference is the UK given our client portfolio.
Fluency in English and local language, if different, required.
Higher education degree or equivalent education, training, and experience.
Preferred 2 years clinical trial experience or medical device.
Required 3-5 years monitoring experience.
Able to work independently once trained.
Good verbal and written communication skills.
Strong organizational skills.
Basic computer proficiency.
Understanding of clinical research processes and regulations.
Certifications such as Society of Clinical Research Associates (SoCRA) or Association of Clinical Research Professionals (ACRP) Certification preferred but not required.

Benefits

Comp & perks

Want to work for NAMSA? Here’s what you get:
Work for a collaborative company culture where you can thrive
Competitive salary
25 days of vacation
Opportunities for personal development and training
Employee wellness program
Chance to make an impact in the medtech industry
Opportunities for advancement within a growing company