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Clinical Trial Associate (m/f)
Eingestellt von Hays aus Mannheim, Universitätsstadt
Gesuchte Skills: Support
Projektbeschreibung
REFERENZNUMMER:
343175/11
IHRE AUFGABEN:
-Effectively support Clinical Trial Managers in daily operational activities related to clinical trials with external Vendors (CRO) and internal stakeholders
-Generate, finalise and distribute study team agendas and meeting minutes in a timely fashion
-Collect, verify and submit clinical study documents on the eTMF/eRoom under the responsibility of the Clinical Trial Manager and ensure eTMF inspection readiness
-Follow up of study budget, preparation and update of purchase orders including management of study invoices
-Update of tracking/reporting and planning tools (e.g. MS Project)
IHRE QUALIFIKATIONEN:
-University/college degree level or equivalent in a relevant discipline
-Profound experience as CTA or comparable operating experience in Pharma/CRO/healthcare with good knowledge of budget and invoicing requirement, as well as drug development process and medical terminology
-Excellent spoken and written English and French
-Team spirit and strong customer service orientation
-Ability to communicate with cross-functional teams
-Strong organizational skills with ability to manage stress, pressure and deadlines
-Good to advanced computer skills with requirement of MS applications
WEITERE QUALIFIKATIONEN:
Qualification/validation specialist
343175/11
IHRE AUFGABEN:
-Effectively support Clinical Trial Managers in daily operational activities related to clinical trials with external Vendors (CRO) and internal stakeholders
-Generate, finalise and distribute study team agendas and meeting minutes in a timely fashion
-Collect, verify and submit clinical study documents on the eTMF/eRoom under the responsibility of the Clinical Trial Manager and ensure eTMF inspection readiness
-Follow up of study budget, preparation and update of purchase orders including management of study invoices
-Update of tracking/reporting and planning tools (e.g. MS Project)
IHRE QUALIFIKATIONEN:
-University/college degree level or equivalent in a relevant discipline
-Profound experience as CTA or comparable operating experience in Pharma/CRO/healthcare with good knowledge of budget and invoicing requirement, as well as drug development process and medical terminology
-Excellent spoken and written English and French
-Team spirit and strong customer service orientation
-Ability to communicate with cross-functional teams
-Strong organizational skills with ability to manage stress, pressure and deadlines
-Good to advanced computer skills with requirement of MS applications
WEITERE QUALIFIKATIONEN:
Qualification/validation specialist
Projektdetails
Geforderte Qualifikationen
-
Kategorie:
Sonstiges