Clinical Trial Monitoring
Site selection, initiation, routine monitoring, and close-out across Phase II-IV studies.
Senior Clinical Research Associate
Clinical trials run safely, compliantly, and on track
I help sponsors and study sites deliver multinational Phase II-IV trials through rigorous monitoring, audit readiness, and cross-functional collaboration.
Get in touchWhat I do
How I can help
A focused look at where I create the most value.
Regulatory Compliance
Oversight aligned with ICH-GCP, ISO 14155:2020, EU-CTR, and FDA requirements.
Data & Audit Readiness
SDV, eCRF review, eTMF documentation, CAPA follow-up, and inspection preparation.
About
14+ Years in Clinical Research
Nadine Obermair — Senior Clinical Research Associate
With 14+ years as a Senior CRA, I have monitored multinational Phase II-IV trials across oncology, allergology, dermatology, autoimmune disease, hematology, respiratory medicine, and neurology.
My approach combines rigorous site oversight, clear cross-functional communication, and hands-on support for audit readiness, regulatory submissions, patient safety, and data integrity.
- Based in
- Holzkirchen, Germany
- Background
- Bioinformatics, biochemistry, clinical research
- Languages
- French, German, English, Spanish
- Focus
- Freelance clinical trial monitoring
Previously at
Clin-Sol GmbH · OPIS GmbH · Syneos Health · SynteractHCR · Roche Pharma · MSD Sharp & Dohme
Contact
Let’s talk
Seeking freelance clinical research collaborations where quality and patient safety matter.
Get in touchHolzkirchen, Germany