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Nathaelle Firmin

@nathaellefirmin

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Clinical research and healthcare professional with 10+ years expertise in clinical operations and patient safety.

France

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What I'm looking for

I seek clinical research roles that leverage my nursing and operations experience, emphasize patient-centered trials, regulatory compliance, and opportunities for multinational, remote collaboration.

I am a bilingual French/English clinical research and healthcare professional with over 10 years' experience across clinical trials, hospital care, and pharmaceutical settings in France, the United Kingdom, and Switzerland. I bring a background as a Registered Nurse with additional qualifications in pharmacy and medical representation, and I am completing a Master’s in Public Health and Ethics.

My core strengths include clinical site coordination, ICH-GCP and regulatory compliance, patient safety and AE/SAE reporting, study logistics and IMP management, and clinical data management using EDC platforms such as Medidata and Oracle. I have acted as primary liaison between investigators, sponsors, and study teams and supported multinational and remote clinical research operations.

I have proven experience in patient coordination, study start-up, protocol implementation, and multidisciplinary collaboration, with a consistent focus on quality, compliance, and participant-centered care. I seek roles where I can leverage clinical and operational expertise to improve trial conduct and patient outcomes.

Experience

Work history, roles, and key accomplishments

Community Nurse

Medicalis

Sep 2024 - Sep 2025 (1 year)

Conducted patient assessments, vital signs monitoring and medication administration while providing therapeutic education and ensuring continuity of care with multidisciplinary teams.

Clinical Documentation

Patient Coordinator

Freelance

Mar 2024 - Jun 2025 (1 year 3 months)

Coordinated patient pathways for remote and decentralized clinical studies as primary patient contact, managing onboarding, scheduling, follow-up and accurate documentation to support protocol compliance.

Patient Coordination Remote Clinical Trials Scheduling Documentation Patient Engagement Oracle

Clinical Site Manager

Ergomed

Jan 2023 - Sep 2024 (1 year 8 months)

Coordinated and supported multiple clinical trial sites across France, the UK, Belgium, and Sweden, ensuring protocol, SOP and ICH-GCP compliance and managing IMP logistics and site issue resolution.

Clinical Site Management ICH GCP IMP Management Regulatory Compliance Sponsor Liaison Remote Monitoring

Clinical Research Nurse

hVivo

Jan 2019 - Jan 2021 (2 years)

Organized and conducted clinical studies in compliance with GCP, managed participant scheduling and procedures, obtained informed consent and performed AE/SAE reporting to support study coordination.

GCP Informed Consent Forms Feasibility Assessment

Registered Nurse

Various Hospitals

Jan 2013 - Jan 2021 (8 years)

Delivered nursing care across acute and interventional radiology settings in the UK and France, coordinating multidisciplinary care, performing assessments, medication administration and clinical monitoring.

Acute Care Nursing Clinical Monitoring Care Coordination Clinical Documentation