Ergomed

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

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

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

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

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

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

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

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

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

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

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

The EDC Developer within the ERGOMED Data Management (DM) department is responsible for all tasks linked to the building of the EDC application for complex projects. The EDC Developer represents a position under direction of the Director of Data Management with oversight by the Projec

The EDC Developer within the ERGOMED Data Management (DM) department is responsible for all tasks linked to the building of the EDC application for complex projects. The EDC Developer represents a position under direction of the Director of Data Management with oversight by the Projec