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
PSI Medical Monitors provide medical input to global clinical studies and advise the teams and business partners while always focusing on patients safety and wellbeing.HomeBased in CanadaResponsibilities:Advise clients project teams sites data safety monitoring boards regulatory More...
Your role in the global Study Startup team will cover three main areas; Departmental support Quality Control and Assurance and Training. Departmental Responsibilities: Maintain trackers for the Study Startup departmentPrepare departmental reportsPlan organize and f More...
Your role in the global Study Startup team will cover three main areas; Departmental support Quality Control and Assurance and Training. Departmental Responsibilities: Maintain trackers for the Study Startup departmentPrepare departmental reportsPlan organize and f More...
Your role in the global Study Startup team will cover three main areas; Departmental support Quality Control and Assurance and Training. Departmental Responsibilities: Maintain trackers for the Study Startup departmentPrepare departmental reportsPlan organize and f More...
Join our international team and be the key support to clinical research projects streamlining communication maintaining systems and managing documents & information.Office location is at Macquarie Park Sydney (Hybrid)The scope of responsibilities will include:Maintenance of databa More...
We are in search of an experienced professional dedicated to developing strategic relationships with clinical research sites with the aim of optimizing and advancing the progress of clinical trials.Office is based in BangkokGeneral Responsibilities: Maintain and refine internal s More...
Your role in the global Study Startup team will cover three main areas; Departmental support Quality Control and Assurance and Training. Departmental Responsibilities: Maintain trackers for the Study Startup departmentPrepare departmental reportsPlan organize and f More...
Your role in the global Study Startup team will cover three main areas; Departmental support Quality Control and Assurance and Training. Departmental Responsibilities: Maintain trackers for the Study Startup departmentPrepare departmental reportsPlan organize and f More...
PSI Medical Monitors provide medical input to global clinical studies and advise the teams and business partners while always focusing on patients safety and wellbeing.HomeBased in the United StatesResponsibilities:Advise clients project teams sites data safety monitoring boards More...
Your role in the global Study Startup team will cover three main areas; Departmental support Quality Control and Assurance and Training.Departmental Responsibilities: Develop tracking tools for the Study Startup departmentPrepare departmental reportsPlan organise and fo More...
As a Senior CRA 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 investigato More...
In this role you will be responsible for managing and optimizing electronic Clinical Outcome Assessment (eCOA) systems for clinical trials. Your expertise will be vital in ensuring their smooth integration and effective implementation which will be key to the success of our projects.Y More...
As part of the PSI team you will have a fair degree of ownership and autonomy to make nuanced countryand departmentspecific adjustments while nurturing the global PSI culture that unites us across six continents. 30%50% travel required for this role approximateYou will:Act a More...
The Site Contract Specialist can be based anywhere in the United States. The core responsibilities of this role include:Facilitating negotiations of site agreements and budgets to ensure alignment with the site activation plan Customizing and preparing country More...
Hybrid position in So Paulo.Only CVs in English will be considered. What you will do:Support PSI in the review of Confidentiality Agreements in different countries including in the U.S.Support the local Legal team in reviewing and drafting simple legal documents (confidentiality More...
Take your career to the next level and be involved in study startup processes in Latam. You will provide direct operational support to project teams and ensure that PSI clinical projects start smoothly and on time. Hybrid position in Buenos AiresOnly CVs in English will be consid More...
Acts as a specialized liaison to assist sites with a protocoltailored approach to increase efficiency of the patient identification and recruitment process. You will be the serving as the face of PSI onsite and plays an important role in the clinical trial process. This is a fieldbase More...
Were searching for a knowledgeable teamoriented Senior CRA to manage the clinical aspects of fullservice 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 trial More...
The scope of responsibilities will include:Constantly maintain and generate relations with Investigative Sites;Maintain and refine the internal site database in cooperation with Study Startup Clinical Operations and Process Improvement;Participate in development of impr More...
Clinical Site Technology Specialist Nuclear Medicine
Not Disclosed
As a Site Technology Specialist you will work with clinical sites and provide technical support and expertise related to technology (Kidney imaging cell therapy radiology and renal ultrasounds).You will:Provide clinical sites with technical support and expertise related to techno More...
