PSI CRO

In this role you will:Lead all biostatistics activities related to clinical trials as responsible project statisticianCommunicate with project teams clients and vendors on statistical questionsDevelop and review statistical sections of protocols including sample size calculationsDevel

In this role you will:Lead all biostatistics activities related to clinical trials as responsible project statisticianCommunicate with project teams clients and vendors on statistical questionsDevelop and review statistical sections of protocols including sample size calculationsDevel

In this role you will:Lead all biostatistics activities related to clinical trials as responsible project statisticianCommunicate with project teams clients and vendors on statistical questionsDevelop and review statistical sections of protocols including sample size calculationsDevel

In this role you will:Lead all biostatistics activities related to clinical trials as responsible project statisticianCommunicate with project teams clients and vendors on statistical questionsDevelop and review statistical sections of protocols including sample size calculationsDevel

In this role you will:Lead all biostatistics activities related to clinical trials as responsible project statisticianCommunicate with project teams clients and vendors on statistical questionsDevelop and review statistical sections of protocols including sample size calculationsDevel

In this role you will:Lead all biostatistics activities related to clinical trials as responsible project statisticianCommunicate with project teams clients and vendors on statistical questionsDevelop and review statistical sections of protocols including sample size calculationsDevel

We are looking for a knowledgeable and proactive Pharmacovigilance Coordinator to join our enthusiastic and vibrant team.In this role you will provide day-to-day support to the companys global Pharmacovigilance Department and In-country Clinical Caretaker (ICCC) in clinical trials wit

We are looking for a knowledgeable and proactive Pharmacovigilance Coordinator to join our enthusiastic and vibrant team.In this role you will provide day-to-day support to the companys global Pharmacovigilance Department and In-country Clinical Caretaker (ICCC) in clinical trials wit

We are looking for a knowledgeable and proactive Pharmacovigilance Coordinator to join our enthusiastic and vibrant team.In this role you will provide day-to-day support to the companys global Pharmacovigilance Department and In-country Clinical Caretaker (ICCC) in clinical trials wit

We are looking for a knowledgeable and proactive Pharmacovigilance Coordinator to join our enthusiastic and vibrant team.In this role you will provide day-to-day support to the companys global Pharmacovigilance Department and In-country Clinical Caretaker (ICCC) in clinical trials wit

In this role you will:Lead all biostatistics activities related to clinical trials as responsible project statisticianCommunicate with project teams clients and vendors on statistical questionsDevelop and review statistical sections of protocols including sample size calculationsDevel

In this role you will:Lead all biostatistics activities related to clinical trials as responsible project statisticianCommunicate with project teams clients and vendors on statistical questionsDevelop and review statistical sections of protocols including sample size calculationsDevel

We are looking for an experienced Senior CRA to support us with the following responsibilities in North Macedonia:Conduct and report SIV RMV COV onsite monitoring visitsPerform CRF review source document verification and query resolutionBe responsible for site communication and manage

We are looking for an experienced Senior CRA to support us with the following responsibilities in North Macedonia:Conduct and report SIV RMV COV onsite monitoring visitsPerform CRF review source document verification and query resolutionBe responsible for site communication and manage

Join our Clinical Operations team and help support the successful delivery of global clinical trials. As a Clinical Operations Administrative Support (COAS) you will provide administrative and operational support to clinical trial project teams helping ensure studies are conducted eff

Join our Clinical Operations team and help support the successful delivery of global clinical trials. As a Clinical Operations Administrative Support (COAS) you will provide administrative and operational support to clinical trial project teams helping ensure studies are conducted eff

Join our Clinical Operations team and help support the successful delivery of global clinical trials. As a Clinical Operations Administrative Support (COAS) you will provide administrative and operational support to clinical trial project teams helping ensure studies are conducted eff

Join our Clinical Operations team and help support the successful delivery of global clinical trials. As a Clinical Operations Administrative Support (COAS) you will provide administrative and operational support to clinical trial project teams helping ensure studies are conducted eff

We are seeking a motivated and detail-oriented Junior IT Systems Administrator to join our IT team in King of Prussia PA. This opportunity is ideal for a current student pursuing a degree in Information Technology Computer Science Information Systems Cybersecurity Networking or a rela

We are seeking a motivated and detail-oriented Junior IT Systems Administrator to join our IT team in King of Prussia PA. This opportunity is ideal for a current student pursuing a degree in Information Technology Computer Science Information Systems Cybersecurity Networking or a rela

The Event Design & Production Specialist supports the creation designing and delivery of clear wellstructured visual materials for corporate and project events trainings and events worldwide.The role offers the opportunity to contribute to highimpact meetings by ensuring all event ass

The Event Design & Production Specialist supports the creation designing and delivery of clear wellstructured visual materials for corporate and project events trainings and events worldwide.The role offers the opportunity to contribute to highimpact meetings by ensuring all event ass

The Event Design & Production Specialist supports the creation designing and delivery of clear wellstructured visual materials for corporate and project events trainings and events worldwide.The role offers the opportunity to contribute to highimpact meetings by ensuring all event ass

The Event Design & Production Specialist supports the creation designing and delivery of clear wellstructured visual materials for corporate and project events trainings and events worldwide.The role offers the opportunity to contribute to highimpact meetings by ensuring all event ass

 Coordinates investigator/ site feasibility and identification process as well as study startup.Monitors project timelines and patient enrollment implements respective corrective and preventive measures.Reviews monitoring visit reports for all visit types and ensures reporting complia

 Coordinates investigator/ site feasibility and identification process as well as study startup.Monitors project timelines and patient enrollment implements respective corrective and preventive measures.Reviews monitoring visit reports for all visit types and ensures reporting complia

We are now expanding Operations and looking for a dynamic and knowledgeable Coordinator to join PSI Grants Expense Management division.Based in Bucharest RomaniaIn this role your goal will be to ensure that physicians and hospitals receive on time and accurate payments for their parti

We are now expanding Operations and looking for a dynamic and knowledgeable Coordinator to join PSI Grants Expense Management division.Based in Bucharest RomaniaIn this role your goal will be to ensure that physicians and hospitals receive on time and accurate payments for their parti

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

As part of PSIs Medical Monitoring team you will join our international group of medical professionals build a career on the frontline of medical science and use your knowledge and expertise to help bring new medications to patients that need them.Full-time employmentPSI Medical Monit

As part of PSIs Medical Monitoring team you will join our international group of medical professionals build a career on the frontline of medical science and use your knowledge and expertise to help bring new medications to patients that need them.Full-time employmentPSI Medical Monit

As a Clinical Research Associate I 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 a

As a Clinical Research Associate I 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 a

Chcesz mieć realny wpływ na rozwój nowoczesnej medycynyDo naszego ośrodka badań klinicznych w Jeleniej Górze poszukujemy osoby która będzie wspierać realizację międzynarodowych badań klinicznych. Jeśli masz już doświadczenie jako Koordynator Badań Klinicznych świetnie! Jeśli natomias

Chcesz mieć realny wpływ na rozwój nowoczesnej medycynyDo naszego ośrodka badań klinicznych w Jeleniej Górze poszukujemy osoby która będzie wspierać realizację międzynarodowych badań klinicznych. Jeśli masz już doświadczenie jako Koordynator Badań Klinicznych świetnie! Jeśli natomias

What Youll DoBuild our presence in the marketDevelop and execute the country expansion strategy.Represent the company within the local clinical research community.Build relationships with key investigators healthcare institutions sponsors CROs and other industry stakeholders.Identify

What Youll DoBuild our presence in the marketDevelop and execute the country expansion strategy.Represent the company within the local clinical research community.Build relationships with key investigators healthcare institutions sponsors CROs and other industry stakeholders.Identify