PSI CRO

Manages the full cycle recruitment process on a regional scaleDevelops posts and maintains job advertisements and recruitment materials tailored to the position and media platformsProactively sources potential candidates via job boards and social media Organizes conducts and reports o

Manages the full cycle recruitment process on a regional scaleDevelops posts and maintains job advertisements and recruitment materials tailored to the position and media platformsProactively sources potential candidates via job boards and social media Organizes conducts and reports o

As Legal Counsel you will provide strategic and hands-on legal support across multiple jurisdictions focusing on corporate employment and clinical trial contracting matters. You will work closely with our global teams and local stakeholders to ensure legal compliance risk mitigation a

As Legal Counsel you will provide strategic and hands-on legal support across multiple jurisdictions focusing on corporate employment and clinical trial contracting matters. You will work closely with our global teams and local stakeholders to ensure legal compliance risk mitigation a

Hybrid role in Mississauga ON CanadaSite 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

Hybrid role in Mississauga ON CanadaSite 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

Hybrid role in Munich GermanyYour responsibilities will involve:Providing administrative support to Medical Affairs departmentPreparing intradepartmental announcements newsletters departmental surveys and presentationsMaintaining departmental tracking and metrics toolsCoordinating dep

Hybrid role in Munich GermanyYour responsibilities will involve:Providing administrative support to Medical Affairs departmentPreparing intradepartmental announcements newsletters departmental surveys and presentationsMaintaining departmental tracking and metrics toolsCoordinating dep

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

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

In this role you will streamline activities of project teams and ensure consistency of Clinical Operations processes across Asia Pacific region. You will ensure meeting study milestones by project teams on a country level report study progress to clients and global stakeholders.The sc

In this role you will streamline activities of project teams and ensure consistency of Clinical Operations processes across Asia Pacific region. You will ensure meeting study milestones by project teams on a country level report study progress to clients and global stakeholders.The sc

The Regional Project Lead is a senior level clinical trial manager who oversees manages and coordinates activities of project teams in designated countries and ensures consistency of Clinical Operations processes across regions. They ensure meeting study milestones are met by the proj

The Regional Project Lead is a senior level clinical trial manager who oversees manages and coordinates activities of project teams in designated countries and ensures consistency of Clinical Operations processes across regions. They ensure meeting study milestones are met by the proj

As a Lead Clinical Research Associate you will hold a leadership role within the study team overseeing and guiding the clinical team while driving trial activities at a country or regional level. You will ensure high-quality execution compliance and timely delivery. You will act as a

As a Lead Clinical Research Associate you will hold a leadership role within the study team overseeing and guiding the clinical team while driving trial activities at a country or regional level. You will ensure high-quality execution compliance and timely delivery. You will act as a

Business Development Representative supports our Business Development team in building and expanding the network of clients.In this role you will Build and sustain long-lasting relationships with existing and potential clients (sponsors CROs medical institutions).Support Site Developm

Business Development Representative supports our Business Development team in building and expanding the network of clients.In this role you will Build and sustain long-lasting relationships with existing and potential clients (sponsors CROs medical institutions).Support Site Developm

The Global Compensation and Benefits Manager is responsible for implementing managing and continuously improving our compensation and benefits programs - supporting our employees and key internal stakeholders. The individual responsible will oversee the day-to-day analysis execution a

The Global Compensation and Benefits Manager is responsible for implementing managing and continuously improving our compensation and benefits programs - supporting our employees and key internal stakeholders. The individual responsible will oversee the day-to-day analysis execution a

The Global Compensation and Benefits Manager is responsible for implementing managing and continuously improving our compensation and benefits programs - supporting our employees and key internal stakeholders. The individual responsible will oversee the day-to-day analysis execution a

The Global Compensation and Benefits Manager is responsible for implementing managing and continuously improving our compensation and benefits programs - supporting our employees and key internal stakeholders. The individual responsible will oversee the day-to-day analysis execution a

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

The Global Compensation and Benefits Manager is responsible for implementing managing and continuously improving our compensation and benefits programs - supporting our employees and key internal stakeholders. The individual responsible will oversee the day-to-day analysis execution a

The Global Compensation and Benefits Manager is responsible for implementing managing and continuously improving our compensation and benefits programs - supporting our employees and key internal stakeholders. The individual responsible will oversee the day-to-day analysis execution a

The Global Compensation and Benefits Manager is responsible for implementing managing and continuously improving our compensation and benefits programs - supporting our employees and key internal stakeholders. The individual responsible will oversee the day-to-day analysis execution a

The Global Compensation and Benefits Manager is responsible for implementing managing and continuously improving our compensation and benefits programs - supporting our employees and key internal stakeholders. The individual responsible will oversee the day-to-day analysis execution a

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

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