Ergomed

The Sr. Director/Director Data Intelligence (ADDI) will support pre-award study feasibility strategy through targeted data gathering and analysis.ROLE AND RESPONSIBILITIES Supports overall operational strategy globally with a focus on our key therapeutic areas of Oncology and Rare Dis

The Sr. Director/Director Data Intelligence (ADDI) will support pre-award study feasibility strategy through targeted data gathering and analysis.ROLE AND RESPONSIBILITIES Supports overall operational strategy globally with a focus on our key therapeutic areas of Oncology and Rare Dis

The role is ideal for a confident and enthusiastic individual who is looking to develop their knowledge of Medical Information. They will assist in the growth of a medical information department in the service provider industry. Knowledge of pharmacovigilance is also an advantage.Resp

The role is ideal for a confident and enthusiastic individual who is looking to develop their knowledge of Medical Information. They will assist in the growth of a medical information department in the service provider industry. Knowledge of pharmacovigilance is also an advantage.Resp

The role is ideal for a confident and enthusiastic individual who is looking to develop their knowledge of Medical Information. They will assist in the growth of a medical information department in the service provider industry. Knowledge of pharmacovigilance is also an advantage.Resp

The role is ideal for a confident and enthusiastic individual who is looking to develop their knowledge of Medical Information. They will assist in the growth of a medical information department in the service provider industry. Knowledge of pharmacovigilance is also an advantage.Resp

The Sr. Director/Director Data Intelligence (ADDI) will support pre-award study feasibility strategy through targeted data gathering and analysis.ROLE AND RESPONSIBILITIES Supports overall operational strategy globally with a focus on our key therapeutic areas of Oncology and Rare Dis

The Sr. Director/Director Data Intelligence (ADDI) will support pre-award study feasibility strategy through targeted data gathering and analysis.ROLE AND RESPONSIBILITIES Supports overall operational strategy globally with a focus on our key therapeutic areas of Oncology and Rare Dis

The role is ideal for a confident and enthusiastic individual who is looking to develop their knowledge of Medical Information. They will assist in the growth of a medical information department in the service provider industry. Knowledge of pharmacovigilance is also an advantage.Resp

The role is ideal for a confident and enthusiastic individual who is looking to develop their knowledge of Medical Information. They will assist in the growth of a medical information department in the service provider industry. Knowledge of pharmacovigilance is also an advantage.Resp

The Sr. Director/Director Data Intelligence (ADDI) will support pre-award study feasibility strategy through targeted data gathering and analysis.ROLE AND RESPONSIBILITIES Supports overall operational strategy globally with a focus on our key therapeutic areas of Oncology and Rare Dis

The Sr. Director/Director Data Intelligence (ADDI) will support pre-award study feasibility strategy through targeted data gathering and analysis.ROLE AND RESPONSIBILITIES Supports overall operational strategy globally with a focus on our key therapeutic areas of Oncology and Rare Dis

The Client Quality Officer is primarily responsible for the implementation and maintenance of the quality system and training for their assigned client projects. Thus ensuring that the project maintains compliance with global regulations legislation PrimeVigilance and client requireme

The Client Quality Officer is primarily responsible for the implementation and maintenance of the quality system and training for their assigned client projects. Thus ensuring that the project maintains compliance with global regulations legislation PrimeVigilance and client requireme

To review and approve post-marketing Individual Case Safety Reports (lCSRs) and Serious Adverse Event (SAE) reports occurring in clinical trials for medical/causality assessment. Review includes coding assessment of seriousness expectedness and Company causality as well as writing of

To review and approve post-marketing Individual Case Safety Reports (lCSRs) and Serious Adverse Event (SAE) reports occurring in clinical trials for medical/causality assessment. Review includes coding assessment of seriousness expectedness and Company causality as well as writing of

Leads the team responsible for ICSR management for a selected project or group of projects as Team Leader Ensures adequate distribution of tasks for assigned projects and teams and oversees the workflow process Assures and exerts of activities leading to effective cooperation with cli

Leads the team responsible for ICSR management for a selected project or group of projects as Team Leader Ensures adequate distribution of tasks for assigned projects and teams and oversees the workflow process Assures and exerts of activities leading to effective cooperation with cli

PrimeVigilance is looking for a Medical Information Associate fluent in English and French to join our growing  Medical Information teamResponsibilities  To provide approved responses to medical enquiries from external customers (healthcare professionals patients pharmaceutical client

PrimeVigilance is looking for a Medical Information Associate fluent in English and French to join our growing  Medical Information teamResponsibilities  To provide approved responses to medical enquiries from external customers (healthcare professionals patients pharmaceutical client

PrimeVigilance is looking for a Medical Information Associate fluent in English and French to join our growing  Medical Information teamResponsibilities  To provide approved responses to medical enquiries from external customers (healthcare professionals patients pharmaceutical client

PrimeVigilance is looking for a Medical Information Associate fluent in English and French to join our growing  Medical Information teamResponsibilities  To provide approved responses to medical enquiries from external customers (healthcare professionals patients pharmaceutical client

PrimeVigilance is looking for a Medical Information Associate fluent in English and French to join our growing  Medical Information teamResponsibilities  To provide approved responses to medical enquiries from external customers (healthcare professionals patients pharmaceutical client

PrimeVigilance is looking for a Medical Information Associate fluent in English and French to join our growing  Medical Information teamResponsibilities  To provide approved responses to medical enquiries from external customers (healthcare professionals patients pharmaceutical client

The Associate Director Tax manages the Groups global tax strategy compliance and advisory functions. The role is responsible for ensuring that all tax obligations are met efficiently accurately and in compliance with applicable laws across multiple jurisdictions. The Associate Directo

The Associate Director Tax manages the Groups global tax strategy compliance and advisory functions. The role is responsible for ensuring that all tax obligations are met efficiently accurately and in compliance with applicable laws across multiple jurisdictions. The Associate Directo

To review and approve post-marketing Individual Case Safety Reports (lCSRs) and Serious Adverse Event (SAE) reports occurring in clinical trials for medical/causality assessment. Review includes coding assessment of seriousness expectedness and company causality as well as writing of

To review and approve post-marketing Individual Case Safety Reports (lCSRs) and Serious Adverse Event (SAE) reports occurring in clinical trials for medical/causality assessment. Review includes coding assessment of seriousness expectedness and company causality as well as writing of

Role and ResponsibilitiesStrategically support and lead the development preparation and tailoring of proposals including supporting strategy development and leading proposal strategy callsLead and assist in the preparation and response to requests for informationRequest screen and imp

Role and ResponsibilitiesStrategically support and lead the development preparation and tailoring of proposals including supporting strategy development and leading proposal strategy callsLead and assist in the preparation and response to requests for informationRequest screen and imp

Role and ResponsibilitiesStrategically support and lead the development preparation and tailoring of proposals including supporting strategy development and leading proposal strategy callsLead and assist in the preparation and response to requests for informationRequest screen and imp

Role and ResponsibilitiesStrategically support and lead the development preparation and tailoring of proposals including supporting strategy development and leading proposal strategy callsLead and assist in the preparation and response to requests for informationRequest screen and imp

The Senior Pharmacovigilance (PV) Physician I is responsible for medical review of ICSRs writing and/or reviewing signal detection reports writing and or reviewing aggregate reports (DSURS PSURS PBRERs. PADERS) reviewing risk management reports (RMPs) and mentoring junior PV Physician

The Senior Pharmacovigilance (PV) Physician I is responsible for medical review of ICSRs writing and/or reviewing signal detection reports writing and or reviewing aggregate reports (DSURS PSURS PBRERs. PADERS) reviewing risk management reports (RMPs) and mentoring junior PV Physician

Responsibilities include:To review and approve post-marketing Individual Case Safety Reports (lCSRs) and Serious Adverse Event (SAE) reports occurring in clinical trials for medical/causality assessment. Review includes coding assessment of seriousness listedness / expectedness and Co

Responsibilities include:To review and approve post-marketing Individual Case Safety Reports (lCSRs) and Serious Adverse Event (SAE) reports occurring in clinical trials for medical/causality assessment. Review includes coding assessment of seriousness listedness / expectedness and Co

Responsibilities include:To review and approve post-marketing Individual Case Safety Reports (lCSRs) and Serious Adverse Event (SAE) reports occurring in clinical trials for medical/causality assessment. Review includes coding assessment of seriousness listedness / expectedness and Co

Responsibilities include:To review and approve post-marketing Individual Case Safety Reports (lCSRs) and Serious Adverse Event (SAE) reports occurring in clinical trials for medical/causality assessment. Review includes coding assessment of seriousness listedness / expectedness and Co

Role and ResponsibilitiesStrategically support and lead the development preparation and tailoring of proposals including supporting strategy development and leading proposal strategy callsLead and assist in the preparation and response to requests for informationRequest screen and imp

Role and ResponsibilitiesStrategically support and lead the development preparation and tailoring of proposals including supporting strategy development and leading proposal strategy callsLead and assist in the preparation and response to requests for informationRequest screen and imp