Ergomed

The Senior Director / Executive Director Medical Writing is a senior management position member of the Senior Leadership Team; Acts as Head of PV Medical Writing Group and has primary responsibility to ensure the contracted PV activities are appropriately performed in line with compan

The Senior Director / Executive Director Medical Writing is a senior management position member of the Senior Leadership Team; Acts as Head of PV Medical Writing Group and has primary responsibility to ensure the contracted PV activities are appropriately performed in line with compan

The Senior Director / Executive Director Medical Writing is a senior management position member of the Senior Leadership Team; Acts as Head of PV Medical Writing Group and has primary responsibility to ensure the contracted PV activities are appropriately performed in line with compan

The Senior Director / Executive Director Medical Writing is a senior management position member of the Senior Leadership Team; Acts as Head of PV Medical Writing Group and has primary responsibility to ensure the contracted PV activities are appropriately performed in line with compan

The Senior Manager Regulatory and PV Delivery is responsible for providing franchise liaison between Ergomed Plc and client on a multiple projects program and actively assist senior management in securing new business by participating to BDMs and contributing to proposals/budgets. The

The Senior Manager Regulatory and PV Delivery is responsible for providing franchise liaison between Ergomed Plc and client on a multiple projects program and actively assist senior management in securing new business by participating to BDMs and contributing to proposals/budgets. The

The Senior Director / Executive Director Medical Writing is a senior management position member of the Senior Leadership Team; Acts as Head of PV Medical Writing Group and has primary responsibility to ensure the contracted PV activities are appropriately performed in line with compan

The Senior Director / Executive Director Medical Writing is a senior management position member of the Senior Leadership Team; Acts as Head of PV Medical Writing Group and has primary responsibility to ensure the contracted PV activities are appropriately performed in line with compan

The Senior Director / Executive Director Medical Writing is a senior management position member of the Senior Leadership Team; Acts as Head of PV Medical Writing Group and has primary responsibility to ensure the contracted PV activities are appropriately performed in line with compan

The Senior Director / Executive Director Medical Writing is a senior management position member of the Senior Leadership Team; Acts as Head of PV Medical Writing Group and has primary responsibility to ensure the contracted PV activities are appropriately performed in line with compan

The Senior Director / Executive Director Medical Writing is a senior management position member of the Senior Leadership Team; Acts as Head of PV Medical Writing Group and has primary responsibility to ensure the contracted PV activities are appropriately performed in line with compan

The Senior Director / Executive Director Medical Writing is a senior management position member of the Senior Leadership Team; Acts as Head of PV Medical Writing Group and has primary responsibility to ensure the contracted PV activities are appropriately performed in line with compan

Acting as the primary contact point for project-related matters Managing clients expectations to make sure the client is satisfied with services of PrimeVigilance and that the work PrimeVigilance delivers meets or even exceeds the clients expectations. Preparing project scope and obje

Acting as the primary contact point for project-related matters Managing clients expectations to make sure the client is satisfied with services of PrimeVigilance and that the work PrimeVigilance delivers meets or even exceeds the clients expectations. Preparing project scope and obje

The Global People Services Associate acts as a support in a central hub for transactional HR activities.  The Global People Services Associate provides efficient consistent support to all employees and managers.Employee Support: Responding to HR-related questions from employees and ma

The Global People Services Associate acts as a support in a central hub for transactional HR activities.  The Global People Services Associate provides efficient consistent support to all employees and managers.Employee Support: Responding to HR-related questions from employees and ma

Study Start Up Specialist coordinates and oversees all activities related to achieving the goal of site activations in accordance with the contract trial protocol and other study specific requirements ICH-GCP all applicable SOPs and regulatory requirements. Study Start Up Specialist t

Study Start Up Specialist coordinates and oversees all activities related to achieving the goal of site activations in accordance with the contract trial protocol and other study specific requirements ICH-GCP all applicable SOPs and regulatory requirements. Study Start Up Specialist t

Providing support to other activities undertaken by the project team on behalf of the client and the company Performing activities in the scope of ICSR management unit within agreed extent and timeframe (including but not limited to): Processing Individual Case Safety Reports (ICSRs)

Providing support to other activities undertaken by the project team on behalf of the client and the company Performing activities in the scope of ICSR management unit within agreed extent and timeframe (including but not limited to): Processing Individual Case Safety Reports (ICSRs)

Carries out assigned administrative duties to support clinical trial conductSets up Investigator Site File according to SOPs provided either by the Sponsor or by ERGOMED and distribute to sitesCoordinates and attends project meetings (e.g. investigator kick-off team etc.) with the PM/

Carries out assigned administrative duties to support clinical trial conductSets up Investigator Site File according to SOPs provided either by the Sponsor or by ERGOMED and distribute to sitesCoordinates and attends project meetings (e.g. investigator kick-off team etc.) with the PM/

PrimeVigilance is looking for a Medical Information Associate with Italian language to be responsible for supporting the Medical Information team in handling initial adverse event and medical information inquiries. Responsibilities: To provide approved responses to medical enquiries f

PrimeVigilance is looking for a Medical Information Associate with Italian language to be responsible for supporting the Medical Information team in handling initial adverse event and medical information inquiries. Responsibilities: To provide approved responses to medical enquiries f

Key Responsibilities:Prepare and manage marketing authorization (MA) submissions including the preparation of local administrative documents quality control (QC) and compilation. Provide ad hoc regulatory advice on submission packages in the post-authorization stage of the medicinal p

Key Responsibilities:Prepare and manage marketing authorization (MA) submissions including the preparation of local administrative documents quality control (QC) and compilation. Provide ad hoc regulatory advice on submission packages in the post-authorization stage of the medicinal p

 Performing activities in the scope of ICSR management unit within agreed extent and timeframe:Processing Individual Case Safety Reports (ICSRs) from all sources in compliance with applicable regulations PrimeVigilance procedures and in accordance with client specific requirements and

 Performing activities in the scope of ICSR management unit within agreed extent and timeframe:Processing Individual Case Safety Reports (ICSRs) from all sources in compliance with applicable regulations PrimeVigilance procedures and in accordance with client specific requirements and

Key Responsibilities:Prepare and manage marketing authorization (MA) submissions including the preparation of local administrative documents quality control (QC) and compilation. Provide ad hoc regulatory advice on submission packages in the post-authorization stage of the medicinal p

Key Responsibilities:Prepare and manage marketing authorization (MA) submissions including the preparation of local administrative documents quality control (QC) and compilation. Provide ad hoc regulatory advice on submission packages in the post-authorization stage of the medicinal p

Engaging in everyday tasks working on tickets and maintaining oversight of personal and group tickets to ensure timely resolution.Closing and meticulously documenting resolutions or workarounds in the internal knowledgebase to facilitate knowledge sharing and improve future problem-so

Engaging in everyday tasks working on tickets and maintaining oversight of personal and group tickets to ensure timely resolution.Closing and meticulously documenting resolutions or workarounds in the internal knowledgebase to facilitate knowledge sharing and improve future problem-so

The Principal Biostatistician is responsible for the design analysis and/or interpretation of clinical studies as a lead (or contributing team members) for clinical this role the Principal Biostatistician will be part of a collaborative team that works with the sponsor PM clinical te

The Principal Biostatistician is responsible for the design analysis and/or interpretation of clinical studies as a lead (or contributing team members) for clinical this role the Principal Biostatistician will be part of a collaborative team that works with the sponsor PM clinical te

 Performing activities in the scope of ICSR management unit within agreed extent and timeframe:Processing Individual Case Safety Reports (ICSRs) from all sources in compliance with applicable regulations PrimeVigilance procedures and in accordance with client specific requirements and

 Performing activities in the scope of ICSR management unit within agreed extent and timeframe:Processing Individual Case Safety Reports (ICSRs) from all sources in compliance with applicable regulations PrimeVigilance procedures and in accordance with client specific requirements and

 Performing activities in the scope of ICSR management unit within agreed extent and timeframe:Processing Individual Case Safety Reports (ICSRs) from all sources in compliance with applicable regulations PrimeVigilance procedures and in accordance with client specific requirements and

 Performing activities in the scope of ICSR management unit within agreed extent and timeframe:Processing Individual Case Safety Reports (ICSRs) from all sources in compliance with applicable regulations PrimeVigilance procedures and in accordance with client specific requirements and

The PV Assistant will be working as part of a project team performing and supporting contracted pharmacovigilance activities on behalf of PrimeVigilance. Previous work experience in pharmacovigilance is not required as you will receive all necessary training from us. If you join Prime

The PV Assistant will be working as part of a project team performing and supporting contracted pharmacovigilance activities on behalf of PrimeVigilance. Previous work experience in pharmacovigilance is not required as you will receive all necessary training from us. If you join Prime