Aktuelle Jobs im Zusammenhang mit Pharmacovigilance Professional - Zürich, Zürich - Cpl Healthcare
-
Zürich, Zürich, Schweiz Takeda VollzeitJob DescriptionTakeda is seeking a highly skilled Vaccines, Director PV Benefit-Risk and Signal Management Physician to join our team in Zurich, Switzerland. As a key member of our global organization, you will be responsible for providing medical support in monitoring the safety profile of assigned vaccine products, ensuring high accuracy and compliance...
-
Healthcare Regulatory Compliance Professional
Vor 4 Tagen
Zürich, Zürich, Schweiz Axiom VollzeitJob Responsibilities:This role involves providing expert advice on regulatory and compliance matters within the healthcare sector. The ideal candidate will have strong analytical and communication skills, proficiency in English, and knowledge of European languages.Key Responsibilities:Develop and implement effective compliance programs.Ensure adherence to...
-
Legal Advisor – Regulatory Affairs in Healthcare
Vor 4 Tagen
Zürich, Zürich, Schweiz Axiom VollzeitJob Overview:Axiom is a global leader in alternative legal services. We offer a highly competitive compensation package and professional development resources.Responsibilities:Provide expert advice on regulatory and compliance matters.Develop and implement compliance programs.Ensure adherence to pharmacovigilance and medical affairs...
-
Senior Manager PV Audits
Vor 7 Tagen
Zürich, Zürich, Schweiz Daiichi Sankyo Europe VollzeitPassion for Innovation. Compassion for Patients. With over 120 years of experience and more than 17,000 employees in over 20 countries, Daiichi Sankyo is dedicated to discovering, developing, and delivering new standards of care that enrich the quality of life around the world. In Europe, we focus on two areas: The goal of our Specialty Business...
-
Zürich, Zürich, Schweiz Axiom VollzeitResponsibilities: Advise on regulatory and compliance matters within the healthcare and pharmaceutical sectors. Develop and implement compliance programs. Ensure adherence to pharmacovigilance and medical affairs regulations. Provide legal counsel on a broad range of issues, including risk management and regulatory affairs. Minimum Qualifications:...
-
Zürich, Zürich, Schweiz Takeda VollzeitBy clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda's Privacy Notice and Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge.Job...
-
Medical Science Liaison Manager Oncology
Vor 4 Tagen
Zürich, Zürich, Schweiz Daiichi Sankyo VollzeitSelect how often (in days) to receive an alert:Medical Science Liaison Manager Oncology (m/f/x) - Region Western Switzerland -Date: 27 Mar 2025Passion for Innovation. Compassion for Patients.With over 120 years of experience and more than 17,000 employees in over 20 countries, Daiichi Sankyo is dedicated to discovering, developing, and delivering new...
-
Vaccine Pharmacovigilance Benefit-risk Scientist
vor 3 Wochen
Zürich, Schweiz Takeda Pharmaceutical Vollzeit**_ OBJECTIVES/PURPOSE: _** Responsible for providing support to Takeda’s Vaccine Pharmacovigilance Department in the monitoring of the safety profile of assigned products within agreed timeframes and to a high standard of accuracy, in compliance with Takeda’s business rules, standard operating procedures and global and local regulatory requirements. -...
-
Senior Manager PV Audits
vor 4 Wochen
Zürich, Schweiz TN Switzerland VollzeitSocial network you want to login/join with:col-narrow-leftClient:Location:Job Category:Other-col-narrow-rightJob Reference:a20cf10ebc9cJob Views:4Posted:03.03.2025Expiry Date:17.04.2025col-wideJob Description:Passion for Innovation. Compassion for Patients.With over 120 years of experience and more than 17,000 employees in over 20 countries, Daiichi Sankyo...
-
Senior Manager PV Audits
vor 2 Wochen
Zürich, Schweiz TN Switzerland VollzeitSocial network you want to login/join with:Client:Location:Job Category:OtherJob Reference:a20cf10ebc9cJob Views:3Posted:14.03.2025Expiry Date:28.04.2025Job Description:Passion for Innovation. Compassion for Patients.With over 120 years of experience and more than 17,000 employees in over 20 countries, Daiichi Sankyo is dedicated to discovering, developing,...
-
Zürich, Schweiz TN Switzerland VollzeitClient: AxiomLocation:Job Category:Job Reference: 0d2511479ccdJob Views: 19Posted: 06.03.2025Expiry Date: 20.04.2025Job Description:Responsibilities:Advise on regulatory and compliance matters within the healthcare and pharmaceutical sectors.Develop and implement compliance programs.Ensure adherence to pharmacovigilance and medical affairs...
-
Zürich, Schweiz WhatJobs VollzeitPassion for Innovation. Compassion for Patients. With over 120 years of experience and more than 17,000 employees in over 20 countries, Daiichi Sankyo is dedicated to discovering, developing, and delivering new standards of care that enrich the quality of life around the world.In Europe, we focus on two areas: The goal of our Specialty Business is to protect...
-
Zürich, Schweiz TN Switzerland VollzeitSocial network you want to login/join with:Client:TakedaLocation:Cambridge, MAJob Category:OtherJob Reference:365b75b92a34Job Views:16Posted:06.03.2025Expiry Date:20.04.2025Job Description:Job Title: Associate Director, Clinical Quality ComplianceAbout the role:As the Associate Director, Clinical Quality Compliance, you will provide quality oversight to the...
Pharmacovigilance Professional
vor 1 Woche
Cpl Healthcare is committed to delivering high-quality patient care, and we are seeking a Pharmacovigilance Professional to play a key role in achieving this goal. As a member of our pharmacovigilance team, you will be responsible for monitoring and evaluating adverse events, ensuring that all reports are submitted to regulatory authorities in compliance with international guidelines (ICH, GVP).
You will work closely with cross-functional teams to prepare and submit pharmacovigilance reports, including PSURs and RMPs. Your expertise in signal detection and trend analysis will enable you to identify and address safety concerns promptly.
This is an excellent opportunity to develop your skills and knowledge in pharmacovigilance and contribute to the delivery of high-quality patient care.
Key Responsibilities:- Monitor and evaluate adverse events, ensuring compliance with international guidelines (ICH, GVP).
- Prepare and submit pharmacovigilance reports, including PSURs and RMPs.
- Conduct signal detection and trend analysis to identify and address safety concerns promptly.
- Stay up-to-date with evolving pharmacovigilance regulations and support internal teams with compliance requirements.
