Medical Data Officer

Excelya

. Collaborate closely with the Study Medical Reviewer .

Posted 10/10/2026full-timeBoulogne-Billancourt • FranceJunior💰 €3,800 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in managing and reviewing clinical data for accuracy and reliability, with a strong focus on medical coding and protocol adherence. Proficient in user acceptance testing and data extraction to support clinical trial milestones.

Highest-signal resume keywords

Medical CodingClinical Trials ExperienceUser Acceptance TestingData ManagementFluency in English

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Medical Coding of Adverse EventsDatabase ValidationClinical Data ReviewStudy Protocol ReviewData Extraction

Soft Skills

Interpersonal SkillsCommunication SkillsOrganizational SkillsCuriosityInvestigation Mindset

Tools & Technologies

ECRFsDatabase Specifications

Certifications & Qualifications

Medical DoctorPharmacist

Industry Keywords

Clinical TrialsTherapeutic DevelopmentSafety ManagementInclusion CriteriaStudy Design

About the role

Key responsibilities & impact

Collaborate closely with the Study Medical Reviewer
Manage and review the medical consistency of reported clinical data
Ensure medical data in databases are accurate, reliable, and analyzable
Review study protocols, especially safety management, coding needs, inclusion and selection criteria, study design, pathology, and mechanism of action of the IMP
Review database specifications and perform user acceptance testing on eCRFs and database validation tools
Participate in identifying and implementing Important Protocol Deviation detection methods, including specifications and UAT
Perform medical coding of adverse events, medical and surgical history, specific events, treatments, and treatment indications
Review medical data entered by investigators using available tools and processes
Create manual queries for clarification, confirmation, or correction when needed
Identify non-serious adverse events according to the study strategy
Handle data extraction to support important study milestones

Requirements

What you’ll need

Junior candidates or preferably 12 months of experience related to clinical trials and therapeutic development
Curiosity and investigation mindset
Good interpersonal and communication skills
Well organized and able to prioritize
Medical Doctor, Pharmacist, or scientist
Fluency in English

Benefits

Comp & perks

Inclusive environment where collaboration and individual growth are encouraged
Stimulating professional environment supporting personal and intellectual growth
Opportunity to evolve through diverse projects
Working alongside preeminent experts
Best employee experience
Community built on company values