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حول Ergomed
We are PrimeVigilance (part of Ergomed Group), a specialised mid-size pharmacovigilance service provider initially established in 2008. We are proud to have achieved global organic growth year after year, with staff based across Europe, North America and Asia all covering services within: Medical Information, Pharmacovigilance, Regulatory Affairs and Quality Assurance.
PrimeVigilance provides first class support to our small to large pharmaceutical and biotechnology partners maintaining long lasting relationships and becoming one of the global leaders in its fields. We cover all therapy areas including medical devices.
We love investing in our staff by providing an excellent training and development platform. We value employee experience, well-being and mental health and we acknowledge that a healthy work life balance is a critical factor for employee satisfaction and in turn nurtures an environment from which a high-quality client service can be achieved.
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123 فرصة عمل في Ergomed
For the Client:To review and approve postmarketing Individual Case Safety Reports (ICSRs) and Serious Adverse Event (SAE) reports occurring in clinical trials for medical/causality assessment. The review includes coding seriousness assessment Company causality and comment listedness/e المزيد...
Provide intelligence on pharmacovigilance requirements and contribute to the development of the strategy and set up activities for projects.Perform regular screening/quality control of regulatory legislative requirements updates worldwide and ensure maintenance of the regula المزيد...
Assures and exerts activities leading to effective cooperation with clients in the area of literature monitoringContributes to achieving companys goals and objectivesEnsures that the Literature Screening responsibilities and activities are managed in a costefficient manner of the high المزيد...
The Specialist/Senior Specialist Study Start Up and Regulatory is responsible for completing study startup and regulatory deliverables based on an established SSU RA management plan. They also serve as a liaison between SSU/regulatory project team authorities vendors and investi المزيد...
The Specialist/Senior Specialist Study Start Up and Regulatory is responsible for completing study startup and regulatory deliverables based on an established SSU RA management plan. They also serve as a liaison between SSU/regulatory project team authorities vendors and investi المزيد...
Due to growth Ergomed is recruiting for an experience CRO Business Development Dircetor.Duties and responsibilitiesInitiates coordinates and develops strategic plans and sales strategies within a specified territory or accounts.Develop account strategies & implementation plans and المزيد...
For the Client:To review and approve postmarketing Individual Case Safety Reports (ICSRs) and Serious Adverse Event (SAE) reports occurring in clinical trials for medical/causality assessment. The review includes coding seriousness assessment Company causality and comment listedness/e المزيد...
The Manager Project Finance is responsible for managing a team of project financial analysts to provide financial and analytical support to the Department Heads and Project Management teams through performance reporting and financial analysis. The Manager will serve as the liaison bet المزيد...
The Manager Project Finance is responsible for managing a team of project financial analysts to provide financial and analytical support to the Department Heads and Project Management teams through performance reporting and financial analysis. The Manager will serve as the liaison bet المزيد...
Manager Project Finance Cropharma Experience Required
The Manager Project Finance is responsible for managing a team of project financial analysts to provide financial and analytical support to the Department Heads and Project Management teams through performance reporting and financial analysis. The Manager will serve as the liaison bet المزيد...
At Ergomed Group we view graphic design as visual storytelling that engages informs and inspires. We seek a skilled Graphic Designer to transform ideas and concepts into compelling visual representations across various media including print digital and social platforms. The ideal cand المزيد...
The Senior Manager of Quality Management is responsible for leading one or more teams within Quality Management in line with global strategic objectives. The Senior Manager of Quality Management collaborates with global operational functions to ensure Pharmacovigilance and Medical Inf المزيد...
Clinical Site Manager Fluent German Speaker Required
Training consultation and support of Study Site Coordinators /Research Nurses on clinical studiesProviding nonoperational site support to ensure progress of clinical study and to ensure that it is conducted recorded and reported in accordance with the protocol standard operating proce المزيد...
Training consultation and support of Study Site Coordinators /Research Nurses on clinical studiesProviding nonoperational site support to ensure progress of clinical study and to ensure that it is conducted recorded and reported in accordance with the protocol standard operating proce المزيد...
The Specialist Regulatory and PV Network is responsible for providing the strategy based on regulatory requirements and for completing regulatory and PV deliverables based on an established PV and regulatory plan. They also serve as a liaison between regulatory and other functional ar المزيد...
Pharmacovigilance Physician Ii - Endocrincology Experience
The Senior Pharmacovigilance (PV) Physician II is responsible for medical review of ICSRs writing and reviewing signal detection reports writing and/or reviewing aggregate reports (DSURS PSURS/PBRERs/PADERS ACOs responses to regulatory authority requests) writing and/or reviewing risk المزيد...
The Senior PV Associate should be a Life science / bio medical background graduate or have other healthcare related degree qualification (chemistry biology biotechnology veterinary science etc.) This is an opportunity for new graduates to start and develop their career within drug saf المزيد...
This is an opportunity for new graduates to start and develop their career within drug safety. The Medical Writing Assistant will be working as part of a medical writing team performing and supporting contracted pharmacovigilance activities on behalf of PrimeVigilanceHandling (trackin المزيد...
This is an opportunity for new graduates to start and develop their career within drug safety. The Medical Writing Assistant will be working as part of a medical writing team performing and supporting contracted pharmacovigilance activities on behalf of PrimeVigilanceHandling (trackin المزيد...
Clinical Site Manager Fluent German Speaker Required
Training consultation and support of Study Site Coordinators /Research Nurses on clinical studiesProviding nonoperational site support to ensure progress of clinical study and to ensure that it is conducted recorded and reported in accordance with the protocol standard operating proce المزيد...
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