At ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance...
Jobs Apply on website Save jobClick to add the job to your shortlist Send job Job summaryChildren and Family Health Devon (CFHD) is the place to be! We are developing an innovative, integrated model of childrens community services and looking for enthusiastic individuals to join our friendly ...
•1 - 5 years’ experience as a clinical data manager in the pharmaceutical industry, especially in global pharma or CRO. •Experience in Phase 1-3 clinical trials, preferably in Oncology and vaccine •Experience in SAS programming required ...
Clario is proud to work with the best in the clinical trial and research pharmacovigilance industry. Learn more about our jobs.
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2. Regulatory Documentation - Independently resolves protocol questions with the Project Manager (PM) and patient related issues with the Medical Monitor (MM). Maintains a record of all contacts with the PM or MM concerning protocol deviations and clarifications. ...
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Regulatory Clinical Affairs Manager 职位 25+ 个职位Regulatory Affairs, Sr. Supervisor/Associate Manager Novo Nordisk 北京市 Regulatory Affairs, Sr. Supervisor/Associate Manager Category: Reg Affairs & Safety Pharmacovigilance Location: Beijing, Beijing, CN... Regulatory Affairs; • Regulatory Compliance;...
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To assist the Quality Manager (QM) and R&D staff in the partner institutions to ensure that all trials sponsored or co-sponsored by the partner organisations are conducted in accordance with the current UK and EU Clinical Trial legislations and the KHP-CTO SOPs. ...