Ergomed

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 Vendor Management Contracts Associate supports the end-to-end administration of vendor contracts and supplier records ensuring contracts are accurately maintained tracked and managed in accordance with company policies and governance requirements. Working closely with Vendor Manag

The Vendor Management Contracts Associate supports the end-to-end administration of vendor contracts and supplier records ensuring contracts are accurately maintained tracked and managed in accordance with company policies and governance requirements. Working closely with Vendor Manag

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 Vendor Management Contracts Associate supports the end-to-end administration of vendor contracts and supplier records ensuring contracts are accurately maintained tracked and managed in accordance with company policies and governance requirements. Working closely with Vendor Manag

The Vendor Management Contracts Associate supports the end-to-end administration of vendor contracts and supplier records ensuring contracts are accurately maintained tracked and managed in accordance with company policies and governance requirements. Working closely with Vendor Manag

The Operations Manager is responsible for optimizing resource planning utilization and operational delivery across consulting implementation managed services and product development engagements. This role serves as the primary link between sales forecasts project delivery and workforc

The Operations Manager is responsible for optimizing resource planning utilization and operational delivery across consulting implementation managed services and product development engagements. This role serves as the primary link between sales forecasts project delivery and workforc

Performs on-site or remote Pre-Study Initiation Interim and Close-Out monitoring visit activities in both Spain and Portugal to ensure that facilities and staff at the investigational site continue to be adequate for the conduct of the studyIdentifies the investigators and verifies th

Performs on-site or remote Pre-Study Initiation Interim and Close-Out monitoring visit activities in both Spain and Portugal to ensure that facilities and staff at the investigational site continue to be adequate for the conduct of the studyIdentifies the investigators and verifies th

Performs on-site or remote Pre-Study Initiation Interim and Close-Out monitoring visit activities in both Spain and Portugal to ensure that facilities and staff at the investigational site continue to be adequate for the conduct of the studyIdentifies the investigators and verifies th

Performs on-site or remote Pre-Study Initiation Interim and Close-Out monitoring visit activities in both Spain and Portugal to ensure that facilities and staff at the investigational site continue to be adequate for the conduct of the studyIdentifies the investigators and verifies th

The Specialist Local RA & PV Network 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 Austral

The Specialist Local RA & PV Network 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 Austral

The Specialist Local RA & PV Network 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 Austral

The Specialist Local RA & PV Network 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 Austral

The Specialist Local RA & PV Network 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 Austral

The Specialist Local RA & PV Network 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 Austral

The Specialist Local RA & PV Network 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 Austral

The Specialist Local RA & PV Network 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 Austral

The Specialist Local RA & PV Network 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 Austral

The Specialist Local RA & PV Network 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 Austral

The Specialist Local RA & PV Network 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 Austral

The Specialist Local RA & PV Network 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 Austral

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.  Responsibilities  To provide approved responses to medical enquiries (healthcare

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.  Responsibilities  To provide approved responses to medical enquiries (healthcare

PrimeVigilance is looking for a Medical Information Assistant to be responsible for supporting the Medical Information team in handling various administrative duties.  Responsibilities Administration support for meetings invoice activities generating reports Maintenance of Medical Inf

PrimeVigilance is looking for a Medical Information Assistant to be responsible for supporting the Medical Information team in handling various administrative duties.  Responsibilities Administration support for meetings invoice activities generating reports Maintenance of Medical Inf

PrimeVigilance is looking for a Medical Information Assistant to be responsible for supporting the Medical Information team in handling various administrative duties.  Responsibilities Administration support for meetings invoice activities generating reports Maintenance of Medical Inf

PrimeVigilance is looking for a Medical Information Assistant to be responsible for supporting the Medical Information team in handling various administrative duties.  Responsibilities Administration support for meetings invoice activities generating reports Maintenance of Medical Inf

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.  Responsibilities  To provide approved responses to medical enquiries (healthcare

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.  Responsibilities  To provide approved responses to medical enquiries (healthcare

The Site Manager (SM) is engaged in facilitating the conduct of clinical studies. Specific focus is put onpatient related site support with the aim to maximise the utilisation of site staff designated to a givenstudy (e.g. study site coordinator study nurse sub-investigator) through p

The Site Manager (SM) is engaged in facilitating the conduct of clinical studies. Specific focus is put onpatient related site support with the aim to maximise the utilisation of site staff designated to a givenstudy (e.g. study site coordinator study nurse sub-investigator) through p

The Site Manager (SM) is engaged in facilitating the conduct of clinical studies. Specific focus is put onpatient related site support with the aim to maximise the utilisation of site staff designated to a givenstudy (e.g. study site coordinator study nurse sub-investigator) through p

The Site Manager (SM) is engaged in facilitating the conduct of clinical studies. Specific focus is put onpatient related site support with the aim to maximise the utilisation of site staff designated to a givenstudy (e.g. study site coordinator study nurse sub-investigator) through p