Ergomed Group, based in the United Kingdom, is seeking a Study Start Up and Regulatory Affairs Specialist to lead and coordinate all activities to achieve site initiation readiness.
The role provides subject matter expertise in regulatory compliance and serves as a key liaison between internal teams, clients, and external stakeholders, with responsibility for multi-country delivery and timely, compliant documentation.
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Global Study Start-Up & Regulatory Lead 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.
