Top Job - Luzern - 125.000 - 150.000

Senior Pharmacovigilance Strategy Lead. Senior Pharmacovigilance Strategy Lead Votre mission Your mission ? ? Develop and implement a GVP risk based strategy to deliver an audit program and quality assurance oversight model. This includes contributes to development of a risk assessment methodology

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Top Job - Meilen

Zulassungsbehörden, Beantwortung von Behördenfragen Zusammenarbeit und Vertretung anderer Stellen im regulatorischen Bereich (z.B. Pharmacovigilance, Werbemittelfreigabe) Aktive Zusammenarbeit mit anderen Abteilungen Sicherstellung der Compliance

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Top Job - Glattbrugg - 60.000 - 80.000

Candidates is holding a university degree in pharmacovigilance or life sciences field in addition to the following experience - 1-drug safety operations - Fluency in English, French and one additional language

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Gestern - Luzern - Spring Professional

For our client, based in Luzern, Spring professional is looking for a highly motivated individual for the role of Pharmacovigilance Specialist in Human Health. The Pharmacovigilance (PV) Specialist is responsible for the day-to-day case management activities in Switzerland, including compliance

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09.02.18 - Luzern

Our partner company, a pharmaceutical market leader is currently looking for a Senior Pharmacovigilance Strategy Lead. Senior Pharmacovigilance Strategy Lead Votre mission Your mission ? ? Develop and implement a GVP risk based strategy to deliver an audit program and quality assurance oversight

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Gestern - Meilen, Zürich - Stettler Consulting AG

Zulassungsbehörden, Beantwortung von Behördenfragen Zusammenarbeit und Vertretung anderer Stellen im regulatorischen Bereich (z.B. Pharmacovigilance, Werbemittelfreigabe) Aktive Zusammenarbeit mit anderen Abteilungen Sicherstellung der Compliance

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Gestern - Genève - Spring Professional

Update and review internal regulatory SOPs. • Assist in answering to medical information requests. • Assist in reviewing and approving promotional materials for Switzerland. • Assist in preparing product's reimbursement dossiers for Switzerland. • Assist the Local Safety Officer in pharmacovigilance

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19.02.18 - Lausanne

Ensures adherence to Good Clinical Practices, pharmacovigilance standards, standard operating procedures and to all other quality standards in conducting research PROFILE Medical Doctor (M.D.) or equivalent of M.D. degree At least 3 years of clinical trial experience in the pharmaceutical industry

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19.02.18 - Lausanne - 200.000 +

In these activities as required - Ensures adherence to Good Clinical Practices, pharmacovigilance standards, standard operating procedures and to all other quality standards in conducting research - Medical Doctor (M.D.) or equivalent of M.D. degree​ - At least 3 years of clinical trial experience in

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19.02.18 - Basel (Basel-Stadt) - 200.000 +

Biosimilar trial execution. - Develop expertise and ensure quality and compliance with GCP and Pharmacovigilance requirements. - Provide oversight on quality and compliance in collaboration with Clinical Quality Assurance and ensure coordination of responses to audit issues. - Lead Clinical Trial Teams in

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18.02.18 - Neuchâtel - 100.000 - 125.000

3-years experience in medical safety/ pharmacovigilance as safety associate Good knowledge in EU pharmacovigilance (GVP) Experience in using a Safety database (e.g. Argus) Very detail-oriented Excellent organization, communication, and inter-personal skills Bsc in Life Science or equivalent acquired

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18.02.18 - Lausanne - 200.000 +

Acts as a clinical interface and actively solicits opinion leader interactions related to the study partners with Medical Affairs, Commercial and other functions in these activities as required Ensures adherence to Good Clinical Practices, pharmacovigilance standards, standard operating procedures and

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18.02.18 - Basel (Basel-Stadt) - 80.000 - 100.000

Standards and processes related to clinical development and safety/pharmacovigilance. To develop Standards, Policies and SOPs, from identification of needs, to execution of development and deployment of outputs and materials. Main Responsibilities Support establishment of GxP Standards, Policies & SOP

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Top Job - Neuchâtel - 80.000 - 100.000

Assessment - Keeping working documents for operational activities up-to-date - Organizing and conducting safety training for successful implementation of collection channel Requirements - 3-years experience in medical safety/ pharmacovigilance as safety associate - Good knowledge in EU pharmacovigilance

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Top Job - Basel (Basel-Stadt)

United Kingdom, England, Welwyn Garden City, Hertfordshire Switzerland, Basel-Town, Basel Germany, Baden Württemberg, Grenzach Pharmacovigilance (PV) Governance & Policy is responsible for Regulatory Requirement Intelligence and governance of the PV System as well as supporting the QPPV in

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