PSI CRO

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.Were looking for a Regulatory Specialist on a المزيد...

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:Act as the main line of communication between the project team spon المزيد...

OperationsDevelops global enrollment and retention solutions to increase patient screening randomization and complianceBuilds and manages patient engagement service offerings and associated costs for global bids including vendor and in-house resource allocationDesigns and implements p المزيد...

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 المزيد...

As a Therapeutic Strategy Lead you will be responsible for the strategic development of PSIs core indications and serves as a core support function to the Associate and Director Therapeutic Strategy.Therapeutic Area SupportSupport indication-specific strategy planning and implementati المزيد...

Office-based in Tbilisi GeorgiaFull-Cycle AccountingProcess all daily accounting transactions including vendor invoices payments bank entries journal postings and intercompany transactions.Maintain accurate records across general ledger accounts payable accounts receivable fixed asset المزيد...

Were searching for a knowledgeable team-oriented CRA II to manage the clinical aspects of full-service global projects in Taiwan. As a CRA II at PSI you will work on the frontline of communication with project stakeholders ensuring timelines targets and standards of clinical المزيد...

Were searching for a knowledgeable team-oriented and proactive leader to supervise the clinical aspects of full-service global projects in Korea. As a Lead CRA at PSI you will work on the frontline of communication with project stakeholders ensuring the successful conduct of المزيد...

Were searching for a knowledgeable team-oriented CRA II to manage the clinical aspects of full-service global projects in Australia. As a CRA II at PSI you will work on the frontline of communication with project stakeholders ensuring timelines targets and standards of clini المزيد...

As a Clinical Supplies Specialist you will be contributing to the smooth conduct of global clinical trials ensuring high-quality clinical supplies flow and be involved in something new outstanding and challenging.Hybrid role in Kyiv UkraineResponsibilities:Clinical study sup المزيد...

Were searching for a knowledgeable team-oriented Senior CRA to manage the clinical aspects of full-service 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 tri المزيد...

We are looking for professional qualified and enthusiastic candidates to take up a full-time position of a Coordinator of the Project Expense Management department. Full-time employment in Tbilisi GeorgiaScope of responsibilitiesVerification and processing of country expense المزيد...

Are you an experienced Clinical Research Professional looking for new development opportunities This might be a great opportunity for you!We have an exciting opening for a Referral Network Specialist which is a dynamic role designed to take your career to the next level. Use your expe المزيد...

As a Clinical Supplies Specialist you will be contributing to the smooth conduct of global clinical trials ensuring high-quality clinical supplies flow and be involved in something new outstanding and challenging.Hybrid role in Prague the Czech RepublicResponsibilities:Clini المزيد...

Assesses feasibility of research protocols based on knowledge and experience and in accordance with designated criteria to select the most suitable studies for the clinical site.  Supervises the conduct of clinical trials in accordance with ICH GCP applicable regulations pro المزيد...

As a Clinical Supplies Specialist you will be contributing to the smooth conduct of global clinical trials ensuring high-quality clinical supplies flow and be involved in something new outstanding and challenging.Hybrid role in Kiev UkraineResponsibilities:Clinical study sup المزيد...

As a Clinical Supplies Specialist you will be contributing to the smooth conduct of global clinical trials ensuring high-quality clinical supplies flow and be involved in something new outstanding and challenging.Hybrid role Sofia BulgariaResponsibilities:Clinical study supp المزيد...

As a Clinical Supplies Specialist you will be contributing to the smooth conduct of global clinical trials ensuring high-quality clinical supplies flow and be involved in something new outstanding and challenging.Hybrid role in Budapest HungaryResponsibilities:Clinical study المزيد...

We are looking for professional qualified and enthusiastic candidates to take up a full-time position of a Junior IT Systems Administrator to provide daily technical support.This is a hybrid role with 2 days per week required in our Oxfordshire officeThe scope of responsibilities will المزيد...

As a Clinical Supplies Specialist you will be contributing to the smooth conduct of global clinical trials ensuring high-quality clinical supplies flow and be involved in something new outstanding and challenging.Hybrid role Bucharest RomaniaResponsibilities:Clinical study s المزيد...