Pharmacovigilance Manager

Your responsibilities include, but not limited to:Leadership:Build strong relationships with relevant functions in the affiliate organization (including but not limited to regulatory affairs, medical affairs, quality assurance, marketing and sales, clinical development and others), in collaboration with the Director Patient Safety HUB/ Associated Director...

Please note, this role is a 2-year contracting position.The PV Intern is responsible for undertaking specified PV activities, including projects, with oversight by their manager or a designated PV colleague.Specific details of tasks may be further described in an addendum to this job description. Activities listed below are applicable for all supported...

Job DescriptionImportant: This role is for a 2-year contract.The PV Intern Role involves specific PV activities, overseen by a manager or designated PV colleague.Tasks may be detailed in an addendum. Activities listed are relevant for all supported countries and can vary based on assignment. Supports local PV processes and activities in collaboration with...

Relevant skills required include:Good verbal and written communication skills with knowledge of medicalterminology.Strong organizational skills, attention to detail and accuracy are important.and resources.Able to build and maintain a network of company contacts and resources to support the Local Safety Unit and its objectives.Acquires knowledge of Global,...

Summary of position: Regulatory: Responsible for:preparation of good quality dossiers and submissions according to specified timelines, in designated countries, to ensure earliest registrations and approvals.preparation, review and approval of product labelling.review and approval of product promotional materials.management of local pharmacovigilance...

With support of other Clinical Research Managers and/or Therapeutic Area Head/Clinical Research Director, this role is accountable for the end-to-end performance and project management for assigned protocols in a country in compliance with ICH/GCP and country regulations, company policies and procedures, quality standards and adverse event reporting...

Gauteng, Midrand- (Market related)Deputy PharmacistMinimum Requirements: Essential: BPharm Qualification. Essential: Registered with The South African Pharmacy Council. At least 2 years of experience in Quality Assurance Management. Experience in submitting dossiers in the CTD (Common Technical Document) format. A minimum of 2 years of experience as a...

Our Clinical Research and Pharmacovigilance team push the boundaries of global healthcare through research and innovation. Through clinical trials and surveillance, we ensure the safety and efficacy of our existing and pipeline products to produce safe, effective, innovative medicine.It is critical that, for all company-sponsored clinical trials, patient...

Our Clinical Research and Pharmacovigilance team push the boundaries of global healthcare through research and innovation. Through clinical trials and surveillance, we ensure the safety and efficacy of our existing and pipeline products to produce safe, effective, innovative medicine.Brief Description of PositionThis role will be key to further develop the...

This role is accountable for performance and compliance for assigned protocols in a country in compliance with ICH/Good Clinical Practice and country regulations, company policies and procedures, quality standards and adverse event reporting requirements internally and externally. Under the oversight of the Sr. Clinical Operations Manager, Head COMs or...

Brief Description of PositionWith support of SrCRA/CRA and/or CRA Manager, acts as primary site contact and site manager throughout all phases of a clinical research study, taking responsibility of allocated sites. - Develops strong site relationships and ensures continuity of site relationships through all phases of the trial. Performs clinical study site...

The role is accountable for performance and compliance for assigned protocols and sites in a country.Under the oversight of the CRA Manager, the person ensures compliance of study conduct with Good Clinical Practice and country regulations, company policies and procedures, quality standards and adverse event reporting requirements internally and...

Brief Description of Position:This role is accountable for performance and compliance for assigned protocols in SOUTH AFRICA and OTHER AFRICAN COUNTRIES in compliance with ICH/GCP and country regulations, our Company's policies and procedures,quality standards and adverse event reporting requirements internally and externally.Under the oversight of the Sr....

Brief Description of Position:This role is accountable for performance and compliance for assigned protocols in a country in compliance with ICH/GCP and country regulations, our Company's policies and procedures, quality standards and adverse event reporting requirements internally and externally. Under the oversight of the Sr. COM, Head COMs or CRD, the...

Job DescriptionThis role is accountable for performance and compliance for assigned protocols in South Africa and Other African Countries in compliance with ICH/GCP and country regulations, our company's policies and procedures, quality standards and adverse event reporting requirements internally and externally. Under the oversight of the COM lead, Head...

Job DescriptionBrief Description of Position:This role is accountable for performance and compliance for assigned protocols in a country in compliance with ICH/GCP and country regulations, company policies and procedures, quality standards and adverse event reporting requirements internally and externally. Under the oversight of the COM Lead, Head COMs or...

Job DescriptionBrief Description of Position:This role is accountable for performance and compliance for assigned protocols in a country in compliance with ICH/GCP and country regulations, company policies and procedures, quality standards and adverse event reporting requirements internally and externally. Under the oversight of the COM Lead, Head COMs or...

Job DescriptionThe role is accountable for performance and compliance for assigned protocols and sites in a country.Under the oversight of the CRA Manager, the person ensures compliance of study conduct with Good Clinical Practice and country regulations, company policies and procedures, quality standards and adverse event reporting requirements internally...

The role is accountable for performance and compliance for assigned protocols and sites in a country. Under the oversight of the CRA Manager, the person ensures compliance of study conduct with Good Clinical Practice and country regulations, company policies and procedures, quality standards and adverse event reporting requirements internally and externally....

Job DescriptionThe role is accountable for performance and compliance for assigned protocols and sites in a country.Under the oversight of the CRA Manager, the person ensures compliance of study conduct with Good Clinical Practice and country regulations, company policies and procedures, quality standards and adverse event reporting requirements internally...