Ergomed
The Study Start Up and Regulatory Affairs Specialist leads and coordinates activities to achieve site initiation readiness, ensuring regulatory compliance and serving as a liaison between internal teams, clients, and external stakeholders. The role involves managing study start-up and regulatory milestones, preparing and reviewing essential documentation, and developing regulatory strategies and plans. This position requires expertise in ICH-GCP and country-specific regulations to support complex clinical trials in rare disease and oncology.
Ergomed Group is a global clinical development partner and contract research organization that helps biotech and pharmaceutical companies bring medicines to market. With a background in co‑development, it offers integrated services including clinical trial management, regulatory affairs, pharmacovigilance, medical affairs and patient recruitment across multiple therapeutic areas. Ergomed positions itself to accelerate development responsibly by combining scientific expertise with operational delivery and flexible partnership models for sponsors worldwide.
Headquarters
San Francisco, CA
Company Size
201-500 employees
Founded
2018
Industry
Technology
Glassdoor Rating
4.2 / 5
Sarah Johnson
Chief Executive Officer
Michael Chen
Chief Technology Officer
Emily Williams
VP of Engineering
David Rodriguez
VP of Product
Jessica Thompson
Chief Financial Officer
Andrew Park
VP of Sales
View leadership team, funding history,
and employee contacts for Ergomed.
Ergomed didn’t post a salary, so this is our estimate from similar listings.
4% below the average for this role
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