Description
Ergomed is hiring a Specialist, Study Start Up and Regulatory Affairs to lead and coordinate site initiation readiness for medium-complexity rare-disease and oncology clinical trials. The role owns regulatory compliance, ICH-GCP documentation, country-specific requirements, site agreements, translations, risk escalation, and regulatory strategy, while serving as a liaison between internal teams, clients, and external stakeholders. Candidates need a graduate degree in Chemistry, Life Sciences, Nursing, or an equivalent combination, plus at least two years of experience in pharmaceutical or CRO industry or a regulatory body.
