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

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

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

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

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

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

This role supports our Business Development team in building and expanding the sites network as well promotes and supports attracting new projects for Milestone One.In this role you will Build and sustain long-lasting relationships with Investigators and Medical Institutions represent

This role supports our Business Development team in building and expanding the sites network as well promotes and supports attracting new projects for Milestone One.In this role you will Build and sustain long-lasting relationships with Investigators and Medical Institutions represent

The Milestone One Site Coordinator role supports a Clinical Study Site in clinical trial related activities according to ICH-GCP protocol requirements within Study specific defined timelines and enrollment goals.The function of the role may include but not limited to any/all of the fo

The Milestone One Site Coordinator role supports a Clinical Study Site in clinical trial related activities according to ICH-GCP protocol requirements within Study specific defined timelines and enrollment goals.The function of the role may include but not limited to any/all of the fo

The Milestone One Site Coordinator role supports a Clinical Study Site in clinical trial related activities according to ICH-GCP protocol requirements within Study specific defined timelines and enrollment goals.The function of the role may include but not limited to any/all of the fo

The Milestone One Site Coordinator role supports a Clinical Study Site in clinical trial related activities according to ICH-GCP protocol requirements within Study specific defined timelines and enrollment goals.The function of the role may include but not limited to any/all of the fo

This role supports our Business Development team in building and expanding the sites network as well promotes and supports attracting new projects for Milestone One.In this role you will Build and sustain long-lasting relationships with Investigators and Medical Institutions represent

This role supports our Business Development team in building and expanding the sites network as well promotes and supports attracting new projects for Milestone One.In this role you will Build and sustain long-lasting relationships with Investigators and Medical Institutions represent

As a CRA II you will work on the frontline of communication with project stakeholders ensuring timelines targets and standards of clinical research projects in a variety of therapeutic indications.  You will build and maintain relationships with clinical sites and investigators.  Your

As a CRA II you will work on the frontline of communication with project stakeholders ensuring timelines targets and standards of clinical research projects in a variety of therapeutic indications.  You will build and maintain relationships with clinical sites and investigators.  Your

As a CRA II you will work on the frontline of communication with project stakeholders ensuring timelines targets and standards of clinical research projects in a variety of therapeutic indications.  You will build and maintain relationships with clinical sites and investigators.  Your

As a CRA II you will work on the frontline of communication with project stakeholders ensuring timelines targets and standards of clinical research projects in a variety of therapeutic indications.  You will build and maintain relationships with clinical sites and investigators.  Your

We are looking for a Senior Compensation Analyst on a fixed-term contract (6-12 months) to implement manage and improve our compensation and benefits programs. The individual responsible will oversee the day-to-day analysis execution and communication of global pay and benefits.Respon

We are looking for a Senior Compensation Analyst on a fixed-term contract (6-12 months) to implement manage and improve our compensation and benefits programs. The individual responsible will oversee the day-to-day analysis execution and communication of global pay and benefits.Respon

We are looking for a Senior Compensation Analyst (6-12 months fixed-term contract) to implement manage and improve our compensation and benefits programs. The individual responsible will oversee the day-to-day analysis execution and communication of global pay and benefits.Responsibil

We are looking for a Senior Compensation Analyst (6-12 months fixed-term contract) to implement manage and improve our compensation and benefits programs. The individual responsible will oversee the day-to-day analysis execution and communication of global pay and benefits.Responsibil

We are looking for a Senior Compensation Analyst (6-12 months fixed-term contract) to implement manage and improve our compensation and benefits programs. The individual responsible will oversee the day-to-day analysis execution and communication of global pay and benefits.Responsibil

We are looking for a Senior Compensation Analyst (6-12 months fixed-term contract) to implement manage and improve our compensation and benefits programs. The individual responsible will oversee the day-to-day analysis execution and communication of global pay and benefits.Responsibil

We are looking for a Senior Compensation Analyst (6-12 months fixed-term contract) to implement manage and improve our compensation and benefits programs. The individual responsible will oversee the day-to-day analysis execution and communication of global pay and benefits.Responsibil

We are looking for a Senior Compensation Analyst (6-12 months fixed-term contract) to implement manage and improve our compensation and benefits programs. The individual responsible will oversee the day-to-day analysis execution and communication of global pay and benefits.Responsibil

We are looking for a Senior Compensation Analyst (6-12 months fixed-term contract) to implement manage and improve our compensation and benefits programs. The individual responsible will oversee the day-to-day analysis execution and communication of global pay and benefits.Responsibil

We are looking for a Senior Compensation Analyst (6-12 months fixed-term contract) to implement manage and improve our compensation and benefits programs. The individual responsible will oversee the day-to-day analysis execution and communication of global pay and benefits.Responsibil