PSI CRO

Were looking for a rockstar Office Administrator/Receptionist to join our Bucharest office! Your mission will include:Manage office operations including supplies equipment and facilitiesProvide exceptional reception services: answer calls greet visitors and handle inquiriesCoordinate More...

We are looking for an experienced CRA ready to train and coordinate junior CRAs on site. Here you will have the opportunity to develop yourself as a trainer mentor and leader. We are committed to develop our employees in their careers by providing tailored courses and mentoring.Respon More...

In this role you will build focus on line management and mentoring of Monitors on project-specific activities.Office-Based in Vienna AustriaThe scope of responsibilities will include:Prepare conduct and report site selection initiation routine monitoring and closeout visits. More...

The Site Administrator is an integral part of the SEO Operations team and supports the daily operations of clinical trials supporting onsite and remote Milestone One staff as assigned. Study-specific delegated tasks will be determined by the Principal Investigator (if applicable) cons More...

OperationsDevelops global enrollment and retention solutions to increase patient screening randomization and complianceBuilds and manages patient engagement service offerings and associated costs for global bids including vendor and in-house resource allocationDesigns and implements p More...

Hybrid role in King of Prussia PA Site ManagementEnsures exchange of information and documentation with sites and vendorsEnsures order receipt inventory storage distribution return/recall and reconciliation of clinical suppliesEnsures regulatory and ethics committee submissions a More...

Hybrid role in Durham NCSite ManagementEnsures exchange of information and documentation with sites and vendorsEnsures order receipt inventory storage distribution return/recall and reconciliation of clinical suppliesEnsures regulatory and ethics committee submissions and notification More...

The Site/Study Coordinator supports a medical institution in clinical trial-related activities. Protocol-specific tasks will be determined by the Principal Investigator considering all local and federal laws and regulations and upon review of competencies observed and documented by Mi More...

The Lead Site/Study Coordinator supports an assigned group of medical institutions for activities involving clinical trial conduct. Support for staff on protocol-specific tasks will be determined by the Principal Investigator considering all local and federal laws and regulations and More...

Office-based in Tbilisi GeorgiaFull-Cycle AccountingProcess all daily accounting transactions including vendor invoices payments bank entries journal postings and intercompany transactions.Maintain accurate records across general ledger accounts payable accounts receivable fixed asset More...

Join our international team and be the key support to clinical research projects as part of the start-up team working in a dynamic multi-functional environment gaining unique skills from various disciplines relevant to clinical research.Office-based or remote in TrkiyeYou will:Co More...

Join our international team and be the key support to clinical research projects streamlining communication maintaining systems and managing documents & information.The scope of responsibilities will include:Maintenance of databases and tracking systemsServes as the primary sites More...

As a Senior CRA at PSI you will enjoy a variety of monitoring tasks and work on clinical studies in different therapeutic indications maintaining the highest quality standards in the industry.Office-based/Hybrid in Seoul South KoreaResponsibilitiesPrepare conduct and report site More...

Were searching for a knowledgeable team-oriented Senior CRA to manage the clinical aspects of full-service global projects in Malaysia. As a Senior CRA at PSI you will work on the frontline of communication with project stakeholders ensuring the successful conduct of clinical tri More...

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.Were looking for a Regulatory Specialist on a More...

As a Therapeutic Strategy Lead you will be responsible for the strategic development of PSIs core indications and serves as a core support function to the Associate and Director Therapeutic Strategy.Therapeutic Area SupportSupport indication-specific strategy planning and implementati More...

Were searching for a knowledgeable team-oriented CRA II to manage the clinical aspects of full-service global projects in Australia. As a CRA II at PSI you will work on the frontline of communication with project stakeholders ensuring timelines targets and standards of clini More...

As a Clinical Research Associate at PSI you will enjoy a variety of monitoring tasks and work on clinical studies in different therapeutic indications maintaining the highest quality standards in the industry.You will:Conduct and report SIV RMV COV onsite monitoring vis More...

The Lead Site/Study Coordinator supports an assigned group of medical institutions for activities involving clinical trial conduct. Support for staff on protocol-specific tasks will be determined by the Principal Investigator considering all local and federal laws and regulations and More...

The Site/Study Coordinator supports a medical institution in clinical trial-related activities. Protocol-specific tasks will be determined by the Principal Investigator considering all local and federal laws and regulations and upon review of competencies observed and documented by Mi More...