PSI CRO

Reporting to the Associate Director RiskBased and Centralized Monitoring the Clinical Data Scientist is an integral part of our team here at PSI. You will work with clinical trials patient and operational data develop new data solutions and set up Riskbased Monitoring systems in Proce المزيد...

Reporting to the Associate Director RiskBased and Centralized Monitoring the Clinical Data Scientist is an integral part of our team here at PSI. You will work with clinical trials patient and operational data develop new data solutions and set up Riskbased Monitoring systems in Proce المزيد...

Reporting to the Associate Director RiskBased and Centralized Monitoring the Clinical Data Scientist is an integral part of our team here at PSI. You will work with clinical trials patient and operational data develop new data solutions and set up Riskbased Monitoring systems in Proce المزيد...

The scope of responsibilities will include:Responsible for correctness and adequateness of company books and bank accountsResponsible for Accounts Receivables i.e. deposits credit card receipts invoicing payments etc.Responsible for billing such as tracking invoicing and followin المزيد...

The Lead Data Manager will be responsible for all data management activities in large complex studies under general supervision or working under minimal supervision on data management activities for small to medium sized projects.  CommunicationPrimary communication point fo المزيد...

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.Location: Bangalore المزيد...

The scope of responsibilities will includeStartup Responsibilities:Is involved with inhouse and onsite activities related to site identification and new clinical trial placement.Is involved in setting clinical trials related collaboration with medical professionals.Ensures comprehensi المزيد...

Please submit your CV in EnglishYou will contribute to statistical programming activities related to global clinical trials work closely with international teams of statisticians programmers and data managers program data sets and summaries.You will:Develop analysis data set المزيد...

Join our international team and be the key support to clinical research projects streamlining communication maintaining systems and managing documents & information. Only CVs in English will be accepted.You will be responsible for:Being the main point of contact between site المزيد...

In this role your goal will be to ensure that physicians and hospitals receive on time and accurate payments for their participation in the global clinical research programs. You will perform various calculations work with payment databases and be the focal point for PSI global teams المزيد...

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 المزيد...

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.Officebased role in Raanana  IsraelYou will:Prepare المزيد...

As a CRA II 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 investigators. Your f المزيد...

Therapeutic OversightIs involved in indicationspecific strategy planning and implementation across the assigned therapeutic areaDevelops best practices based on lessons learnedMentors trains and assists Operations staff in strategies and best practices within their assigned therapeuti المزيد...

Therapeutic OversightIs involved in indicationspecific strategy planning and implementation across the assigned therapeutic areaDevelops best practices based on lessons learnedMentors trains and assists Operations staff in strategies and best practices within their assigned therapeuti المزيد...

Therapeutic OversightIs involved in indicationspecific strategy planning and implementation across the assigned therapeutic areaDevelops best practices based on lessons learnedMentors trains and assists Operations staff in strategies and best practices within their assigned therapeuti المزيد...

Therapeutic OversightIs involved in indicationspecific strategy planning and implementation across the assigned therapeutic areaDevelops best practices based on lessons learnedMentors trains and assists Operations staff in strategies and best practices within their assigned therapeuti المزيد...

Milestone One Site Coordinator supports trial sites in all related activities according to ICHGCP protocol requirements within Study specific defined timelines and enrollment goals.In this role you will:Act as the main line of communication between the Sponsor or CRO and the site المزيد...

Milestone One Site Coordinator supports trial sites in all related activities according to ICHGCP protocol requirements within Study specific defined timelines and enrollment goals.In this role you will:Act as the main line of communication between the Sponsor or CRO and the site المزيد...

Please submit your CV in EnglishYou will contribute to statistical programming activities related to global clinical trials work closely with international teams of statisticians programmers and data managers program data sets and summaries.You will:Develop analysis data set المزيد...