Ergomed Group is seeking a Study Start Up and Regulatory Affairs Specialist (2+ years) for full-time work within our global regulatory unit. You will lead activities to achieve site initiation readiness and ensure regulatory compliance across assigned countries.
You will draft, review and QC regulatory/start-up documentation, liaise with clients and sites, and contribute to SSU strategy while managing timelines and quality standards.
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Regulatory Start-Up Specialist | Rare Disease & Oncology in Guildford employer: Ergomed Group
Ergomed Group is an exceptional employer that fosters a collaborative and innovative work culture, making it an ideal place for professionals in the life sciences field. With a strong commitment to employee growth, we offer comprehensive training and development opportunities, ensuring that our team members can advance their careers while contributing to meaningful projects in the pharmaceutical industry. Located in a vibrant area, Ergomed provides a supportive environment where your expertise in study start-up and regulatory affairs will be valued and rewarded.
