PSI CRO

Clincial Data Manager plays a critical role in the clinical research project. If you are detail-oriented and committed to quality able to work with large volume of clinical or medical data you might be the professional we are looking for.Please submit your CV in EnglishResponsibilitie

Clincial Data Manager plays a critical role in the clinical research project. If you are detail-oriented and committed to quality able to work with large volume of clinical or medical data you might be the professional we are looking for.Please submit your CV in EnglishResponsibilitie

Clincial Data Manager plays a critical role in the clinical research project. If you are detail-oriented and committed to quality able to work with large volume of clinical or medical data you might be the professional we are looking for.Please submit your CV in EnglishResponsibilitie

Clincial Data Manager plays a critical role in the clinical research project. If you are detail-oriented and committed to quality able to work with large volume of clinical or medical data you might be the professional we are looking for.Please submit your CV in EnglishResponsibilitie

Clincial Data Manager plays a critical role in the clinical research project. If you are detail-oriented and committed to quality able to work with large volume of clinical or medical data you might be the professional we are looking for.Please submit your CV in EnglishResponsibilitie

Clincial Data Manager plays a critical role in the clinical research project. If you are detail-oriented and committed to quality able to work with large volume of clinical or medical data you might be the professional we are looking for.Please submit your CV in EnglishResponsibilitie

Clincial Data Manager plays a critical role in the clinical research project. If you are detail-oriented and committed to quality able to work with large volume of clinical or medical data you might be the professional we are looking for.Please submit your CV in EnglishResponsibilitie

Clincial Data Manager plays a critical role in the clinical research project. If you are detail-oriented and committed to quality able to work with large volume of clinical or medical data you might be the professional we are looking for.Please submit your CV in EnglishResponsibilitie

Join our team of experts in regulatory and ethics submissions of clinical studies.  You will focus on facilitating the start of research projects of novel medicinal products while taking a step further in your professional career.Your role:Prepare clinical trial submission dossiers fo

Join our team of experts in regulatory and ethics submissions of clinical studies.  You will focus on facilitating the start of research projects of novel medicinal products while taking a step further in your professional career.Your role:Prepare clinical trial submission dossiers fo

Join our team of experts in regulatory and ethics submissions of clinical studies.  You will focus on facilitating the start of research projects of novel medicinal products while taking a step further in your professional career.Your role:Prepare clinical trial submission dossiers fo

Join our team of experts in regulatory and ethics submissions of clinical studies.  You will focus on facilitating the start of research projects of novel medicinal products while taking a step further in your professional career.Your role:Prepare clinical trial submission dossiers fo

Start your career in clinical research streamlining communication maintaining systems and managing documents.The scope of responsibilities will include:Maintenance of databases and tracking systemsWork with large amount of documents including their compiling procurement processing tra

Start your career in clinical research streamlining communication maintaining systems and managing documents.The scope of responsibilities will include:Maintenance of databases and tracking systemsWork with large amount of documents including their compiling procurement processing tra

Start your career in clinical research streamlining communication maintaining systems and managing documents.The scope of responsibilities will include:Maintenance of databases and tracking systemsWork with large amount of documents including their compiling procurement processing tra

Start your career in clinical research streamlining communication maintaining systems and managing documents.The scope of responsibilities will include:Maintenance of databases and tracking systemsWork with large amount of documents including their compiling procurement processing tra

At PSI Proposal Manager coordinates all phases of PSIs proposal process while maintaining the companys win rate of 30% and higher. You will contribute to everything from RFP strategy to bid defense slide decks.  You will partner with global teams of subject matter experts from Feasibi

At PSI Proposal Manager coordinates all phases of PSIs proposal process while maintaining the companys win rate of 30% and higher. You will contribute to everything from RFP strategy to bid defense slide decks.  You will partner with global teams of subject matter experts from Feasibi

At PSI Proposal Manager coordinates all phases of PSIs proposal process while maintaining the companys win rate of 30% and higher. You will contribute to everything from RFP strategy to bid defense slide decks.  You will partner with global teams of subject matter experts from Feasibi

At PSI Proposal Manager coordinates all phases of PSIs proposal process while maintaining the companys win rate of 30% and higher. You will contribute to everything from RFP strategy to bid defense slide decks.  You will partner with global teams of subject matter experts from Feasibi

We are looking for an experienced freelance Sr. CRA to support us with the following responsibilities in Canada:Conduct and report SIV RMV COV onsite monitoring visitsPerform CRF review source document verification and query resolutionBe responsible for site communication and manageme

We are looking for an experienced freelance Sr. CRA to support us with the following responsibilities in Canada:Conduct and report SIV RMV COV onsite monitoring visitsPerform CRF review source document verification and query resolutionBe responsible for site communication and manageme

We are looking for an experienced freelance Sr. CRA to support us with the following responsibilities in Canada:Conduct and report SIV RMV COV onsite monitoring visitsPerform CRF review source document verification and query resolutionBe responsible for site communication and manageme

We are looking for an experienced freelance Sr. CRA to support us with the following responsibilities in Canada:Conduct and report SIV RMV COV onsite monitoring visitsPerform CRF review source document verification and query resolutionBe responsible for site communication and manageme

Hybrid role in Bucharest RomaniaThe Medical Monitoring Support Specialist plays a key role in supporting the day-to-day operations of the Medical Monitoring department. The position is responsible for coordinating administrative activities maintaining departmental reports and tracking

Hybrid role in Bucharest RomaniaThe Medical Monitoring Support Specialist plays a key role in supporting the day-to-day operations of the Medical Monitoring department. The position is responsible for coordinating administrative activities maintaining departmental reports and tracking

Hybrid role in Bucharest RomaniaThe Medical Monitoring Support Specialist plays a key role in supporting the day-to-day operations of the Medical Monitoring department. The position is responsible for coordinating administrative activities maintaining departmental reports and tracking

Hybrid role in Bucharest RomaniaThe Medical Monitoring Support Specialist plays a key role in supporting the day-to-day operations of the Medical Monitoring department. The position is responsible for coordinating administrative activities maintaining departmental reports and tracking