Ergomed

At PrimeVigilance PV Officers are independent case processing team members who are expected to manage a variety of case processing services with full accountability.  If you join PrimeVigilance you can expect to work with teams of different sizes from small clinical trial to large gen

At PrimeVigilance PV Officers are independent case processing team members who are expected to manage a variety of case processing services with full accountability.  If you join PrimeVigilance you can expect to work with teams of different sizes from small clinical trial to large gen

The Senior Specialist Regulatory and PV Network is responsible for developing the strategy based on regulatory requirements and for driving regulatory and PV deliverables based on an established PV and regulatory plan. They also serve as a liaison between regulatory and other function

The Senior Specialist Regulatory and PV Network is responsible for developing the strategy based on regulatory requirements and for driving regulatory and PV deliverables based on an established PV and regulatory plan. They also serve as a liaison between regulatory and other function

The Senior Specialist Regulatory and PV Network is responsible for developing the strategy based on regulatory requirements and for driving regulatory and PV deliverables based on an established PV and regulatory plan. They also serve as a liaison between regulatory and other function

The Senior Specialist Regulatory and PV Network is responsible for developing the strategy based on regulatory requirements and for driving regulatory and PV deliverables based on an established PV and regulatory plan. They also serve as a liaison between regulatory and other function

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

Role and Responsibilities Supports Regional People Generalist or Regional People Advisor - Sending out contracts entering new hire data onto HR system.  Preparing induction packs for new joiners  Supporting with the probation review process Manage the leaver processes and coordinating

Role and Responsibilities Supports Regional People Generalist or Regional People Advisor - Sending out contracts entering new hire data onto HR system.  Preparing induction packs for new joiners  Supporting with the probation review process Manage the leaver processes and coordinating

As we continue to grow we are looking to hire a Junior Accountant to join our growing Finance Department in Zagreb.The Junior Accountant role is a varied one covering various accounting responsibilities:Posting business transactions process invoices employee expense claims and verify

As we continue to grow we are looking to hire a Junior Accountant to join our growing Finance Department in Zagreb.The Junior Accountant role is a varied one covering various accounting responsibilities:Posting business transactions process invoices employee expense claims and verify

Plan conduct and report GxP audits including technology focused and computerised systems audits as applicable across Pharma Biotech and Healthcare client base.Deliver consultancy services relating to regulated technologies including governance models system oversight risk assessments

Plan conduct and report GxP audits including technology focused and computerised systems audits as applicable across Pharma Biotech and Healthcare client base.Deliver consultancy services relating to regulated technologies including governance models system oversight risk assessments

The Benefit/Risk Officer should be a Life science / bio medical background graduate preferably pharmacist with an experience in signal detection and use of signal management tools. The Benefit/Risk Officer will be working as part of a project team performing and supporting contracted

The Benefit/Risk Officer should be a Life science / bio medical background graduate preferably pharmacist with an experience in signal detection and use of signal management tools. The Benefit/Risk Officer will be working as part of a project team performing and supporting contracted

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/

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/

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