Ergomed

ADAMAS Consulting is looking for PV Auditor on a freelance basis to cover audits across Europe. Both full and part time (0.6 FTE) will be considered Planning preparation conduct reporting and follow up (including CAPA plans) of various types of Pharmacovigilance (PV) audits according

ADAMAS Consulting is looking for PV Auditor on a freelance basis to cover audits across Europe. Both full and part time (0.6 FTE) will be considered Planning preparation conduct reporting and follow up (including CAPA plans) of various types of Pharmacovigilance (PV) audits according

ADAMAS Consulting is looking for PV Auditor on a freelance basis to cover audits across Europe. Both full and part time (0.6 FTE) will be considered Planning preparation conduct reporting and follow up (including CAPA plans) of various types of Pharmacovigilance (PV) audits according

ADAMAS Consulting is looking for PV Auditor on a freelance basis to cover audits across Europe. Both full and part time (0.6 FTE) will be considered Planning preparation conduct reporting and follow up (including CAPA plans) of various types of Pharmacovigilance (PV) audits according

The RA & PV specialist will act as Local Country Person Responsible for Pharmacovigilance and Regulatory Affairs (LCPPV/LCPRA) and serves as the primary local RA&PV representative to ensure compliance with national pharmacovigilance and regulatory requirements in Australia. This posit

The RA & PV specialist will act as Local Country Person Responsible for Pharmacovigilance and Regulatory Affairs (LCPPV/LCPRA) and serves as the primary local RA&PV representative to ensure compliance with national pharmacovigilance and regulatory requirements in Australia. This posit

The RA & PV specialist will act as Local Country Person Responsible for Pharmacovigilance and Regulatory Affairs (LCPPV/LCPRA) and serves as the primary local RA&PV representative to ensure compliance with national pharmacovigilance and regulatory requirements in Australia. This posit

The RA & PV specialist will act as Local Country Person Responsible for Pharmacovigilance and Regulatory Affairs (LCPPV/LCPRA) and serves as the primary local RA&PV representative to ensure compliance with national pharmacovigilance and regulatory requirements in Australia. This posit

Bridges the gap between individual project delivery and overarching program strategy managing clusters of related projects.ROLE AND RESPONSIBILITIES Coordinate PMO activities as directed Manage project scope schedule and costs Maintain good client relations Oversee task delivery and i

Bridges the gap between individual project delivery and overarching program strategy managing clusters of related projects.ROLE AND RESPONSIBILITIES Coordinate PMO activities as directed Manage project scope schedule and costs Maintain good client relations Oversee task delivery and i

Work closely with Line Managers to develop a strong understanding of the open positions and maintain communication regarding vacancy status Create enticing job adverts and publish them across multiple job boards in multiple regions using the ATS one click publishing tool.Execute an ap

Work closely with Line Managers to develop a strong understanding of the open positions and maintain communication regarding vacancy status Create enticing job adverts and publish them across multiple job boards in multiple regions using the ATS one click publishing tool.Execute an ap

Assists with set up and maintenance of the Trial Master File (TMF). Serves as main point of contact for all TMF-related activities for assigned projects. Processing and indexing of project documents for the TMF in accordance with project-specific guidelines and relevant SOPs. Upon stu

Assists with set up and maintenance of the Trial Master File (TMF). Serves as main point of contact for all TMF-related activities for assigned projects. Processing and indexing of project documents for the TMF in accordance with project-specific guidelines and relevant SOPs. Upon stu

PrimeVigilance is looking for a Medical Information Associate to be responsible for supporting the Medical Information team in handling initial adverse event and medical information inquiries in English.  Key Responsibilities  To provide approved responses to medical enquiries from ex

PrimeVigilance is looking for a Medical Information Associate to be responsible for supporting the Medical Information team in handling initial adverse event and medical information inquiries in English.  Key Responsibilities  To provide approved responses to medical enquiries from ex

PrimeVigilance is looking for a Medical Information Associate 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 (healthcare profession

PrimeVigilance is looking for a Medical Information Associate 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 (healthcare profession

We are looking to strengthen our growing Medical Information Management Team. The role will be focused on supporting a Medical Information Team in the delivery of Medical Information Services.  The successful applicant will be responsible for client communication and service delivery

We are looking to strengthen our growing Medical Information Management Team. The role will be focused on supporting a Medical Information Team in the delivery of Medical Information Services.  The successful applicant will be responsible for client communication and service delivery

Ensure that projects are delivered on time within budget and agreed scope maintaining the appropriate industry sponsor and Ergomed quality standards Liaise with project team members provide training where needed and ensure correct allocation to tasks Develop review and edit project pl

Ensure that projects are delivered on time within budget and agreed scope maintaining the appropriate industry sponsor and Ergomed quality standards Liaise with project team members provide training where needed and ensure correct allocation to tasks Develop review and edit project pl

PrimeVigilance is looking for a Medical Information Associate with Dutch 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 fro

PrimeVigilance is looking for a Medical Information Associate with Dutch 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 fro

PrimeVigilance is looking for a Medical Information Associate with Dutch 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 fro

PrimeVigilance is looking for a Medical Information Associate with Dutch 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 fro

PrimeVigilance is looking for a Medical Information Associate with Dutch 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 fro

PrimeVigilance is looking for a Medical Information Associate with Dutch 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 fro

The role is ideal for a confident and enthusiastic individual with an understanding of Medical Information who is looking to develop or build on their knowledge and gain exposure in assisting in the growth of a medical information department in the service provider industry. Knowledge

The role is ideal for a confident and enthusiastic individual with an understanding of Medical Information who is looking to develop or build on their knowledge and gain exposure in assisting in the growth of a medical information department in the service provider industry. Knowledge

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) from all sources in compliance with applicable regulations PrimeVigilance procedures and in accordance with c

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) from all sources in compliance with applicable regulations PrimeVigilance procedures and in accordance with c

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) from all sources in compliance with applicable regulations PrimeVigilance procedures and in accordance with c

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) from all sources in compliance with applicable regulations PrimeVigilance procedures and in accordance with c

The Senior Specialist Study Start Up and Regulatory Affairs leads and coordinates all activities related to achieving site initiation readiness. The role provides subject matter expertise ensures regulatory compliance and serves as a key liaison between internal teams clients and exte

The Senior Specialist Study Start Up and Regulatory Affairs leads and coordinates all activities related to achieving site initiation readiness. The role provides subject matter expertise ensures regulatory compliance and serves as a key liaison between internal teams clients and exte

Due to the continued growth of our Global Study Start Up Group we are now seeking a Site Contracts Manager who will be responsible for overseeing the negotiation process of clinical study agreements on assigned trials and who will act as a subject matter expert to our sponsors and sta

Due to the continued growth of our Global Study Start Up Group we are now seeking a Site Contracts Manager who will be responsible for overseeing the negotiation process of clinical study agreements on assigned trials and who will act as a subject matter expert to our sponsors and sta

The Senior Specialist Study Start Up and Regulatory Affairs leads and coordinates all activities related to achieving site initiation readiness. The role provides subject matter expertise ensures regulatory compliance and serves as a key liaison between internal teams clients and exte

The Senior Specialist Study Start Up and Regulatory Affairs leads and coordinates all activities related to achieving site initiation readiness. The role provides subject matter expertise ensures regulatory compliance and serves as a key liaison between internal teams clients and exte