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You will be a contributor to a Global Team with collective responsibility for regulatory activities associated with global pharmacovigilance including electronic pharmacovigilance system, adverse drug experience (ADE) reports, trending reports, ADE
Support the Medical Information function at Idorsia and provide product specific expertise. Additionally, this role contributes to various Medical Information projects and processes such as content generation, enquiry escalation handling, metric reports,
The role includes hands on GVP QA activities such as support to our many stakeholders as well as performing audits alone or together with own team members or with support from neighboring teams. You will take the role as QA
Define medical strategy in line with company ambition and cluster scorecard/priorities. Assess, design, and lead all medical activities including research programs, clinical trials, RWE programs, data mining projects, and all data generation activities.
Ensuring the highest quality standards from subcontractors in line with current regulations and good practices (GxP), and delivery of reliable clinical data within agreed timelines. Oversight of early‑phase clinical trials (Phase I–II) in