Global Study Start-Up & Regulatory Lead
Washington, District of Columbia, 20022, USA
Listed on 2026-10-06
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Healthcare
Ergomed Group is seeking a Specialist, Study Start Up and Regulatory Affairs to lead and coordinate activities ensuring site initiation readiness across assigned regions. You will provide expert regulatory input and ensure compliance with ICH-GCP and country-specific requirements.
You will draft, review, and manage regulatory submissions, site agreements, translations, and essential documents while guiding internal teams, clients, and external stakeholders to timely delivery.
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We aim to respond to suitable candidates as soon as possible.
Full responsibilities and requirements are described in the listing above.
Learn more about the Global Study Start-Up & Regulatory Lead role in the description above.
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