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Risk Management Plans Manager
Eingestellt von Harvey Nash IT Recruitment Switzerland
Gesuchte Skills: Client, Network
Projektbeschreibung
For our Client in ROTKREUZ, we are looking for a RISK MANAGEMENT PLANS MANAGER/MEDICAL INFORMATION CENTER MANAGER (RMP MANAGER, MIC MANAGER), for a 12 MONTHS contract.
Duration: 16/07/2018 to 16/06/2019
Location: Rotkreuz
Workload 100%
Job purpose:
The Medical Information Center (MIC) is the entry point for all medical and scientific questions and issues for non-promoted brands. Drives and monitors the local implementation of global Safety Risk Management Plans (RMP) and local amendments to these plans as required.
Major Responsibilities for RMP:
- Drives the local execution of the RMP for all Gen Med, Oncology Pharma and Vaccines products in the Swiss CPO
- Manage/oversee CPO RMP commitment status tracking activities in COSTA (Commitment Status Tracking Application)
- Provides input as required by Global RMP Office, DS&E Management and QPPV on implementation status of local RMP commitments
- As member of the Global/Regional RMP Network, provides input to global RMP Office and CPOs/countries
Major Responsibilities for MIC:
- Set up and roll out MI Strategy.
- Enhance customer focused MI according to the company's standards.
- Quality check and review of BPI/CDS update implementation in the CPO in collaboration with DRA for non-promoted products.
- Provide reports for reconciliation.
- Act as Medical Expert for established products of the therapeutic area in cooperation with the global Medical Expert.
- Continued professional development via keeping up-to-date on trends and developments in the wider MI function, including information resources.
- Prepare a long-term plan for MI activities aligned with the needs of internal and external customers through annual analysis of customer needs.
- Is core member of the Established Medicines Committee (EMC).
- Represent the company's MIC in Pharma Industry events to network and learn.
Candidate's Profile:
Linguistic background:
- LANGUAGE GERMAN & FRENCH ARE A MUST (WRITTEN & SPOKEN),
- ENGLISH B/C1
Work experience:
MUST-HAVES:
- PHARMACEUTICAL BACKGROUND
- CLIENT ORIENTATION
- KNOW-HOW IN DIFFERENT SYSTEMS, MUTLI-CLINICAL TOPICS (DIGITAL)
- KNOWLEDGE OF NATIONAL AND INTERNATIONAL REGULATIONS FOR PHARMACOVIGILANCE
- KNOWLEDGE OF PHARMACOLOGICAL AND MEDICAL TERMINOLOGY.
- Excellent communications, interpersonal and negotiation skills
- Quality and focus oriented
- Computer knowledge
- Additional educational requirements as may be man-dated by national requirements
Education: A degree in medicine, veterinary medicine, pharmacy, health discipline or life sciences
For further details please contact Aleksandra Sztajerowska.
Duration: 16/07/2018 to 16/06/2019
Location: Rotkreuz
Workload 100%
Job purpose:
The Medical Information Center (MIC) is the entry point for all medical and scientific questions and issues for non-promoted brands. Drives and monitors the local implementation of global Safety Risk Management Plans (RMP) and local amendments to these plans as required.
Major Responsibilities for RMP:
- Drives the local execution of the RMP for all Gen Med, Oncology Pharma and Vaccines products in the Swiss CPO
- Manage/oversee CPO RMP commitment status tracking activities in COSTA (Commitment Status Tracking Application)
- Provides input as required by Global RMP Office, DS&E Management and QPPV on implementation status of local RMP commitments
- As member of the Global/Regional RMP Network, provides input to global RMP Office and CPOs/countries
Major Responsibilities for MIC:
- Set up and roll out MI Strategy.
- Enhance customer focused MI according to the company's standards.
- Quality check and review of BPI/CDS update implementation in the CPO in collaboration with DRA for non-promoted products.
- Provide reports for reconciliation.
- Act as Medical Expert for established products of the therapeutic area in cooperation with the global Medical Expert.
- Continued professional development via keeping up-to-date on trends and developments in the wider MI function, including information resources.
- Prepare a long-term plan for MI activities aligned with the needs of internal and external customers through annual analysis of customer needs.
- Is core member of the Established Medicines Committee (EMC).
- Represent the company's MIC in Pharma Industry events to network and learn.
Candidate's Profile:
Linguistic background:
- LANGUAGE GERMAN & FRENCH ARE A MUST (WRITTEN & SPOKEN),
- ENGLISH B/C1
Work experience:
MUST-HAVES:
- PHARMACEUTICAL BACKGROUND
- CLIENT ORIENTATION
- KNOW-HOW IN DIFFERENT SYSTEMS, MUTLI-CLINICAL TOPICS (DIGITAL)
- KNOWLEDGE OF NATIONAL AND INTERNATIONAL REGULATIONS FOR PHARMACOVIGILANCE
- KNOWLEDGE OF PHARMACOLOGICAL AND MEDICAL TERMINOLOGY.
- Excellent communications, interpersonal and negotiation skills
- Quality and focus oriented
- Computer knowledge
- Additional educational requirements as may be man-dated by national requirements
Education: A degree in medicine, veterinary medicine, pharmacy, health discipline or life sciences
For further details please contact Aleksandra Sztajerowska.
Projektdetails
Geforderte Qualifikationen
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Kategorie:
IT Entwicklung