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RMP Manager & MIC Manager
Eingestellt von Harvey Nash IT Recruitment Switzerland
Projektbeschreibung
Harvey Nash is looking for a RMP Manager & MIC Manager for a 1 + month project in Switzerland.
The role is for a candidate to drive and monitor the local implementation of global Safety Risk Management Plans (RMP) and to be responsible for the provision of timely, accurate and balanced medical/scientific and technical information to external and internal customers
As RMP Manager you are responsible for:
. Driving the local execution of the RMP for all Gen Med, Oncology Pharma and Vaccines products in the Swiss CPO
. Managing/overseeing CPO RMP commitment status tracking activities in COSTA (Commitment Status Tracking Application)
. Providing input as required by Global RMP Office, DS Reviewing response with supervisor or Medical Expert as appropriate
. Managing MI Databases: Reviewing standard answers on a regular basis, doing quality check of data bases and developing new standard documents as appropriate
. Providing reports for reconciliation with QA and DS good working knowledge of local language; knowledge of other languages desirable
. Knowledge of national and international regulations for pharmacovigilance
. Knowledge of pharmacological and medical terminology
For more information, please contact:
Moritz Dewald
The role is for a candidate to drive and monitor the local implementation of global Safety Risk Management Plans (RMP) and to be responsible for the provision of timely, accurate and balanced medical/scientific and technical information to external and internal customers
As RMP Manager you are responsible for:
. Driving the local execution of the RMP for all Gen Med, Oncology Pharma and Vaccines products in the Swiss CPO
. Managing/overseeing CPO RMP commitment status tracking activities in COSTA (Commitment Status Tracking Application)
. Providing input as required by Global RMP Office, DS Reviewing response with supervisor or Medical Expert as appropriate
. Managing MI Databases: Reviewing standard answers on a regular basis, doing quality check of data bases and developing new standard documents as appropriate
. Providing reports for reconciliation with QA and DS good working knowledge of local language; knowledge of other languages desirable
. Knowledge of national and international regulations for pharmacovigilance
. Knowledge of pharmacological and medical terminology
For more information, please contact:
Moritz Dewald
Projektdetails
Geforderte Qualifikationen
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Kategorie:
Sonstiges