Dieses Jobangebot ist archiviert und steht nicht mehr zur Verfügung.
Vakante Jobangebote finden Sie unter Projekte.
Vakante Jobangebote finden Sie unter Projekte.
Senior Clinical Operations Manager (m/f)
Eingestellt von Hays aus Mannheim, Universitätsstadt
Gesuchte Skills: Support
Projektbeschreibung
REFERENZNUMMER:
376667/11
IHRE AUFGABEN:
-Directs the planning, set-up and conduct of trials (phase 1 to phase 3)
-Prepares trial budgets, forecasts, timelines, and project plans
-Negotiates contracts and budgets for assigned clinical trials
-Support close CRO surveillance and management of other third party vendors
-Reviews clinical study protocols and provides input
-Prepares clinical trial supplies projections and ensures the availability of a supply chain during the whole conduct of the trial
-Supervises training programs to assure consistency and compliance in conduct and monitoring of clinical trials
-Prepares status reports for assigned clinical trials
-Participates in internal/external audits
IHRE QUALIFIKATIONEN:
-Profound and progressively increasing clinical development experience within the pharmaceutical industry
-Experience in clinical operations/clinical trial management especially in outsourced global phase 3 trials
-Monitoring experience
-Advanced academic degree (M.S., PhD or MD) is preferred; at the minimum an academic degree in Life Sciences, Pharmacy or Medicine is required
-Communication skills (fluency in English mandatory)
WEITERE QUALIFIKATIONEN:
Clinical project manager
376667/11
IHRE AUFGABEN:
-Directs the planning, set-up and conduct of trials (phase 1 to phase 3)
-Prepares trial budgets, forecasts, timelines, and project plans
-Negotiates contracts and budgets for assigned clinical trials
-Support close CRO surveillance and management of other third party vendors
-Reviews clinical study protocols and provides input
-Prepares clinical trial supplies projections and ensures the availability of a supply chain during the whole conduct of the trial
-Supervises training programs to assure consistency and compliance in conduct and monitoring of clinical trials
-Prepares status reports for assigned clinical trials
-Participates in internal/external audits
IHRE QUALIFIKATIONEN:
-Profound and progressively increasing clinical development experience within the pharmaceutical industry
-Experience in clinical operations/clinical trial management especially in outsourced global phase 3 trials
-Monitoring experience
-Advanced academic degree (M.S., PhD or MD) is preferred; at the minimum an academic degree in Life Sciences, Pharmacy or Medicine is required
-Communication skills (fluency in English mandatory)
WEITERE QUALIFIKATIONEN:
Clinical project manager
Projektdetails
Geforderte Qualifikationen
-
Kategorie:
Sonstiges