About PSI CRO
PSI is a leading full-service global Contract Research Organization whose key strength is predictable patient enrollment across multiple therapeutic areas. PSI is known in the industry as a CRO focused on on-time project delivery. This is achieved through investing substantial effort and MD resources into performing quality feasibility assessments that provide an accurate predictor of study timelines. PSIs global reach allows us to run clinical trials across multiple continents, in 50+ countries around the world. PSIs reputation is that of a 'no-nonsense'? CRO focused on timely patient enrollment and project delivery. An exceptionally high repeat and referral business rates alongside low staff turnover are indicative of our commitment to be the best CRO in the world as measured by our clients and our employees. http://www.psi-cro.com
320 Job openings in Psi Cro
Join our international team and support regulatory aspects of clinical research projects streamlining communication maintaining electronic systems and managing documents.OfficeBased in RaananaYou will:Be the point of contact for clinical project teams and support services on regu More...
Freelance Cra Experienced Clinical Trials Professional
Not Disclosed
Were looking for experienced clinical trials professional to coordinate clinical trials on site and support our Business Development team in building and expanding the network of clients.In this role you will:Act as the main line of communication between the Sponsor or CRO and th More...
Hybrid role in King of Prussia PASite 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 not More...
Clincial Data Manager plays a critical role in the clinical research project. If you are detailoriented and committed to quality able to work with large volume of clinical or medical data you might be the professional we are looking for.Responsibilities will include:Track database set More...
If you are a qualified enthusiastic legal professional you may be the expert we are looking for to join our dynamic team in Toronto Canada.This role supports PSIs legal with a primary focus on contracts related to clinical research. As an Associate Legal Counsel you will work closely More...
Hybrid role in Research Triangle Park 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 More...
Clincial Data Manager plays a critical role in the clinical research project. If you are detailoriented and committed to quality able to work with large volume of clinical or medical data you might be the professional we are looking for.Responsibilities will include:Track database set More...
We are currently growing in Bulgaria and looking for a Clinical Data Manager to join our global team.Clincial Data Manager plays a critical role in the clinical research project. If you are detailoriented and committed to quality able to work with large volume of clinical or medical d More...
Actively prospects and leverages potential new business opportunities within specified Customer/Accounts.Cultivates strong longterm relationships with key decisionmakers with Account and develops deep knowledge of the Customer/Account organization.Analyzes potential opportunitie More...
Actively prospects and leverages potential new business opportunities within specified Customer/Accounts.Cultivates strong longterm relationships with key decisionmakers with Account and develops deep knowledge of the Customer/Account organization.Analyzes potential opportunitie 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 all types of onsite monitoring visitsBe involved More...
Take your career to the next level and manage clinical study startup activities in Japan. You will share your expert knowledge develop clinical project startup strategies provide operational support and ensure that PSI projects start smoothly and on time. Office based in Shanghai More...
With the industry moving forward the central monitoring function has become a top priority at PSI. We are looking for a person who would lead the riskbased monitoring approach implementation on the clinical study and program level to ensure patient safety and data integrity.You will:L More...
Take your career to the next level and be involved in study startup processes in the US. You will provide direct operational support to project teams and ensure that PSI clinical projects start smoothly and on time. HomebasedYou will:Supports all processes critical for site activ More...
We are looking for experienced clinical trials monitoring professionals to support us with new sites activation identification and onsite trial coordinating. Your tasks:Act as the main line of communication between the Sponsor or CRO and the site.Ensure response to feas 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.Hybrid working arrangement in Bucharest RomaniaYou More...
With the industry moving forward the central monitoring function has become a top priority at PSI. We are looking for a person who would lead the riskbased monitoring approach implementation on the clinical study and program level to ensure patient safety and data integrity.You will:L More...
If you are ready to manage the feasibility process within deliverable timelines act as an expert regarding clinical site capacities ensure high standards of feasibility assessment and patient recruitment strategies and be involved in something new outstanding and challenging this job More...
With the industry moving forward the central monitoring function has become a top priority at PSI. We are looking for a person who would lead the riskbased monitoring approach implementation on the clinical study and program level to ensure patient safety and data integrity.You will:L More...
With the industry moving forward the central monitoring function has become a top priority at PSI. We are looking for a person who would lead the riskbased monitoring approach implementation on the clinical study and program level to ensure patient safety and data integrity.You will:L More...
