Ergomed

For the Client:To review and approve post-marketing 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/

For the Client:To review and approve post-marketing 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/

For the Client:To review and approve post-marketing 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/

For the Client:To review and approve post-marketing 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/

For the Client:To review and approve post-marketing 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/

For the Client:To review and approve post-marketing 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/

For the Client:To review and approve post-marketing 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/

For the Client:To review and approve post-marketing 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/

Support Project Managers in managing finance of multiple projects. Coordination with vendors Project team and finance team for timely receipt and posting of transactions. Budgeting and tracking the budget spend monthly annually or complete life of the project. Find gaps if any betwee

Support Project Managers in managing finance of multiple projects. Coordination with vendors Project team and finance team for timely receipt and posting of transactions. Budgeting and tracking the budget spend monthly annually or complete life of the project. Find gaps if any betwee

For the Client:To review and approve post-marketing 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/

For the Client:To review and approve post-marketing 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/

This role requires working and supporting group of Project Managers who lead one or several pharmacovigilance (PV) project teams performing contracted pharmacovigilance activities on behalf of PrimeVigilance clients.Role and ResponsibilitiesManagement and support of a team of Project

This role requires working and supporting group of Project Managers who lead one or several pharmacovigilance (PV) project teams performing contracted pharmacovigilance activities on behalf of PrimeVigilance clients.Role and ResponsibilitiesManagement and support of a team of Project

Performs on-site or remote Pre-Study Initiation Interim and Close-Out monitoring visit activities to ensure that facilities and staff at the investigational site continue to be adequate for the conduct of the study Identifies the investigators and verifiesthat the investigator has ade

Performs on-site or remote Pre-Study Initiation Interim and Close-Out monitoring visit activities to ensure that facilities and staff at the investigational site continue to be adequate for the conduct of the study Identifies the investigators and verifiesthat the investigator has ade

Performs on-site or remote Pre-Study Initiation Interim and Close-Out monitoring visit activities to ensure that facilities and staff at the investigational site continue to be adequate for the conduct of the study Identifies the investigators and verifiesthat the investigator has ade

Performs on-site or remote Pre-Study Initiation Interim and Close-Out monitoring visit activities to ensure that facilities and staff at the investigational site continue to be adequate for the conduct of the study Identifies the investigators and verifiesthat the investigator has ade

Performs on-site or remote Pre-Study Initiation Interim and Close-Out monitoring visit activities to ensure that facilities and staff at the investigational site continue to be adequate for the conduct of the study Identifies the investigators and verifiesthat the investigator has ade

Performs on-site or remote Pre-Study Initiation Interim and Close-Out monitoring visit activities to ensure that facilities and staff at the investigational site continue to be adequate for the conduct of the study Identifies the investigators and verifiesthat the investigator has ade

Performs on-site or remote Pre-Study Initiation Interim and Close-Out monitoring visit activities to ensure that facilities and staff at the investigational site continue to be adequate for the conduct of the study Identifies the investigators and verifiesthat the investigator has ade

Performs on-site or remote Pre-Study Initiation Interim and Close-Out monitoring visit activities to ensure that facilities and staff at the investigational site continue to be adequate for the conduct of the study Identifies the investigators and verifiesthat the investigator has ade

The Data Manager within the ERGOMED Data Management (DM) is responsible for database testing query management management of lab reference ranges serious adverse event reconciliation vendor data reconciliation and other tasks related to data management. The Data Manager represents a po

The Data Manager within the ERGOMED Data Management (DM) is responsible for database testing query management management of lab reference ranges serious adverse event reconciliation vendor data reconciliation and other tasks related to data management. The Data Manager represents a po

Main responsibilities:Assume leadership and functional representation for projects of medium/high complexity ensuring effective and rapid coordination and management of regulatory deliverables driving the team to meet the agreed targets and to comply with the agreed procedures tracker

Main responsibilities:Assume leadership and functional representation for projects of medium/high complexity ensuring effective and rapid coordination and management of regulatory deliverables driving the team to meet the agreed targets and to comply with the agreed procedures tracker

The position is primarily responsible for the creation and maintenance of client Pharmacovigilance System Master Files in line with global regulations legislation PrimeVigilance and Client requirements.The position will maintain and manage PSMF for clientsActivities will include PSMF:

The position is primarily responsible for the creation and maintenance of client Pharmacovigilance System Master Files in line with global regulations legislation PrimeVigilance and Client requirements.The position will maintain and manage PSMF for clientsActivities will include PSMF:

The position is primarily responsible for the creation and maintenance of client Pharmacovigilance System Master Files in line with global regulations legislation PrimeVigilance and Client requirements.The position will maintain and manage PSMF for clientsActivities will include PSMF:

The position is primarily responsible for the creation and maintenance of client Pharmacovigilance System Master Files in line with global regulations legislation PrimeVigilance and Client requirements.The position will maintain and manage PSMF for clientsActivities will include PSMF:

The position is primarily responsible for the creation and maintenance of client Pharmacovigilance System Master Files in line with global regulations legislation PrimeVigilance and Client requirements.The position will maintain and manage PSMF for clientsActivities will include PSMF:

The position is primarily responsible for the creation and maintenance of client Pharmacovigilance System Master Files in line with global regulations legislation PrimeVigilance and Client requirements.The position will maintain and manage PSMF for clientsActivities will include PSMF:

Assures and exerts activities leading to effective cooperation with clients in the area of ICSR ManagementContributes to achieving companys goals and objectivesWorks under supervision of more experienced colleagueProviding support to other activities undertaken by the project team on

Assures and exerts activities leading to effective cooperation with clients in the area of ICSR ManagementContributes to achieving companys goals and objectivesWorks under supervision of more experienced colleagueProviding support to other activities undertaken by the project team on

The position is primarily responsible for the creation and maintenance of client Pharmacovigilance System Master Files in line with global regulations legislation PrimeVigilance and Client requirements.The position will maintain and manage PSMF for clientsActivities will include PSMF:

The position is primarily responsible for the creation and maintenance of client Pharmacovigilance System Master Files in line with global regulations legislation PrimeVigilance and Client requirements.The position will maintain and manage PSMF for clientsActivities will include PSMF:

The position is primarily responsible for the creation and maintenance of client Pharmacovigilance System Master Files in line with global regulations legislation PrimeVigilance and Client requirements.The position will maintain and manage PSMF for clientsActivities will include PSMF:

The position is primarily responsible for the creation and maintenance of client Pharmacovigilance System Master Files in line with global regulations legislation PrimeVigilance and Client requirements.The position will maintain and manage PSMF for clientsActivities will include PSMF:

The position is primarily responsible for the creation and maintenance of client Pharmacovigilance System Master Files in line with global regulations legislation PrimeVigilance and Client requirements.The position will maintain and manage PSMF for clientsActivities will include PSMF:

The position is primarily responsible for the creation and maintenance of client Pharmacovigilance System Master Files in line with global regulations legislation PrimeVigilance and Client requirements.The position will maintain and manage PSMF for clientsActivities will include PSMF: