Ergomed

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

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

The PrimeVigilance medical writer position offers a unique opportunity to further develop your career in the field of drug safety.Key ResponsibilitiesIndependent authoring editing and reviewing of various regulatory/clinical documents (e.g. aggregate reports risk management plans and

The PrimeVigilance medical writer position offers a unique opportunity to further develop your career in the field of drug safety.Key ResponsibilitiesIndependent authoring editing and reviewing of various regulatory/clinical documents (e.g. aggregate reports risk management plans and

If you join PrimeVigilance you will work with teams of various sizes from small clinical trial projects to large post-marketing teams.We seek proactive capable and motivated individuals who aim to exceed expectations.PrimeVigilanceにご入社いただくと臨床試験から市販後までさまざまな規模のチームでご活躍いただきます当社では主体的で能力が高

If you join PrimeVigilance you will work with teams of various sizes from small clinical trial projects to large post-marketing teams.We seek proactive capable and motivated individuals who aim to exceed expectations.PrimeVigilanceにご入社いただくと臨床試験から市販後までさまざまな規模のチームでご活躍いただきます当社では主体的で能力が高

The Associate Director Start Up and Regulatory Affairs oversees and contributes to the day-to-day start-up and regulatory operations provides input on new business development opportunities develop and maintain relationships with clients and provide guidance and support in regards to

The Associate Director Start Up and Regulatory Affairs oversees and contributes to the day-to-day start-up and regulatory operations provides input on new business development opportunities develop and maintain relationships with clients and provide guidance and support in regards to

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

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

The Quality Assurance Coordinator works with the PrimeVigilance Quality Assurance group  to support the group with quality activities related to administrative tasks including compiling tracking and retrieval of information planning department organisation and archiving. Role and Resp

The Quality Assurance Coordinator works with the PrimeVigilance Quality Assurance group  to support the group with quality activities related to administrative tasks including compiling tracking and retrieval of information planning department organisation and archiving. Role and Resp

Reception duties and administrative tasksAnswering phone callsGreeting and assisting guestsHandling incoming and outgoing mailCoordination with suppliersMonitoring and ordering office suppliesPerforming other office-related tasksQualifications : Availability at least 20 hours per wee

Reception duties and administrative tasksAnswering phone callsGreeting and assisting guestsHandling incoming and outgoing mailCoordination with suppliersMonitoring and ordering office suppliesPerforming other office-related tasksQualifications : Availability at least 20 hours per wee

The PrimeVigilance medical writer position offers a unique opportunity to further develop your career in the field of drug safety.Key ResponsibilitiesIndependent authoring editing and reviewing of various regulatory/clinical documents (e.g. aggregate reports risk management plans and

The PrimeVigilance medical writer position offers a unique opportunity to further develop your career in the field of drug safety.Key ResponsibilitiesIndependent authoring editing and reviewing of various regulatory/clinical documents (e.g. aggregate reports risk management plans and

The Associate Director Start Up and Regulatory Affairs oversees and contributes to the day-to-day start-up and regulatory operations provides input on new business development opportunities develop and maintain relationships with clients and provide guidance and support in regards to

The Associate Director Start Up and Regulatory Affairs oversees and contributes to the day-to-day start-up and regulatory operations provides input on new business development opportunities develop and maintain relationships with clients and provide guidance and support in regards to

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

The Data Manager within the ERGOMED Data Management (DM) is responsible for database testing query management management of lab reference ranges serious adverse event reconciliation vendor data reconciliation and other tasks related to data management. The Data Manager represents a po

The Data Manager within the ERGOMED Data Management (DM) is responsible for database testing query management management of lab reference ranges serious adverse event reconciliation vendor data reconciliation and other tasks related to data management. The Data Manager represents a po

The Associate Director Start Up and Regulatory Affairs oversees and contributes to the day-to-day start-up and regulatory operations provides input on new business development opportunities develop and maintain relationships with clients and provide guidance and support in regards to

The Associate Director Start Up and Regulatory Affairs oversees and contributes to the day-to-day start-up and regulatory operations provides input on new business development opportunities develop and maintain relationships with clients and provide guidance and support in regards to

The Local Country Person Responsible for Pharmacovigilance and Regulatory Affairs (LCPPV/LCPRA) serves as the primary local representative to ensure compliance with national pharmacovigilance and regulatory requirements. This dual-role position is responsible for executing PV and RA a

The Local Country Person Responsible for Pharmacovigilance and Regulatory Affairs (LCPPV/LCPRA) serves as the primary local representative to ensure compliance with national pharmacovigilance and regulatory requirements. This dual-role position is responsible for executing PV and RA a

The Associate Director Start Up and Regulatory Affairs oversees and contributes to the day-to-day start-up and regulatory operations provides input on new business development opportunities develop and maintain relationships with clients and provide guidance and support in regards to

The Associate Director Start Up and Regulatory Affairs oversees and contributes to the day-to-day start-up and regulatory operations provides input on new business development opportunities develop and maintain relationships with clients and provide guidance and support in regards to

The PrimeVigilance medical writer position offers a unique opportunity to further develop your career in the field of drug safety.Key ResponsibilitiesIndependent authoring editing and reviewing of various regulatory/clinical documents (e.g. aggregate reports risk management plans and

The PrimeVigilance medical writer position offers a unique opportunity to further develop your career in the field of drug safety.Key ResponsibilitiesIndependent authoring editing and reviewing of various regulatory/clinical documents (e.g. aggregate reports risk management plans and

The Quality Assurance Coordinator works with the PrimeVigilance Quality Assurance group  to support the group with quality activities related to administrative tasks including compiling tracking and retrieval of information planning department organisation and archiving. Role and Resp

The Quality Assurance Coordinator works with the PrimeVigilance Quality Assurance group  to support the group with quality activities related to administrative tasks including compiling tracking and retrieval of information planning department organisation and archiving. Role and Resp

The PrimeVigilance Senior Medical Writer role offers a unique opportunity to further develop your career in the field of drug safety. You will be working in an international team of experienced aggregate report writers contributing to further departmental growth. Key ResponsibilitiesI

The PrimeVigilance Senior Medical Writer role offers a unique opportunity to further develop your career in the field of drug safety. You will be working in an international team of experienced aggregate report writers contributing to further departmental growth. Key ResponsibilitiesI

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

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