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Clinical Trial Assistant (m/f)
Eingestellt von Hays aus Mannheim, Universitätsstadt
Gesuchte Skills: Support
Projektbeschreibung
REFERENZNUMMER:
249191/11
IHRE AUFGABEN:
-Support the Global Clinical Project Management Team administratively in all phases of the conduct of a clinical trial
-Assist in the coordination of Global Clinical Project Management Team meetings, Clinical Trial Team meetings, and other meetings (e.g., Investigator meetings) by developing the agendas, preparing materials/presentations, and preparing meeting minutes
-Set-up and maintain protocol and site level trackers (e.g., Investigator list, regulatory documents, secrecy agreements, monitoring visits)
-Track and distribute trial supplies (e.g. digital pens, Case Report Forms, bulk supplies)
-Support the Global Clinical Project Management team by preparing and maintaining trial communication tools (e.g. website, newsletters, pocket brochures, safety letters, enrollment graphs)
-Generate and distribute regulatory packages
-Provide administrative support to the TDS group as needed
-Assist in the coordination of meetings with the Global Event group and the Clinical Trial team
-Other duties, activities, and projects as assigned
IHRE QUALIFIKATIONEN:
-Clinical research related experience with knowledge of applicable regulations and guidelines
-Ability to implement team decisions
-Good problem-solving skills
-Superior organizational skills with ability to organize own time and the workload of others
-Ability to coordinate activities efficiently under pressure
WEITERE QUALIFIKATIONEN:
Clinical trial assistant
249191/11
IHRE AUFGABEN:
-Support the Global Clinical Project Management Team administratively in all phases of the conduct of a clinical trial
-Assist in the coordination of Global Clinical Project Management Team meetings, Clinical Trial Team meetings, and other meetings (e.g., Investigator meetings) by developing the agendas, preparing materials/presentations, and preparing meeting minutes
-Set-up and maintain protocol and site level trackers (e.g., Investigator list, regulatory documents, secrecy agreements, monitoring visits)
-Track and distribute trial supplies (e.g. digital pens, Case Report Forms, bulk supplies)
-Support the Global Clinical Project Management team by preparing and maintaining trial communication tools (e.g. website, newsletters, pocket brochures, safety letters, enrollment graphs)
-Generate and distribute regulatory packages
-Provide administrative support to the TDS group as needed
-Assist in the coordination of meetings with the Global Event group and the Clinical Trial team
-Other duties, activities, and projects as assigned
IHRE QUALIFIKATIONEN:
-Clinical research related experience with knowledge of applicable regulations and guidelines
-Ability to implement team decisions
-Good problem-solving skills
-Superior organizational skills with ability to organize own time and the workload of others
-Ability to coordinate activities efficiently under pressure
WEITERE QUALIFIKATIONEN:
Clinical trial assistant
Projektdetails
Geforderte Qualifikationen
-
Kategorie:
Sonstiges