PSI CRO

The Site/Study Coordinator supports a medical institution in clinical trial-related activities. Protocol-specific tasks will be determined by the Principal Investigator considering all local and federal laws and regulations and upon review of competencies observed and documented by Mi المزيد...

The Site Administrator is an integral part of the SEO Operations team and supports the daily operations of clinical trials supporting onsite and remote Milestone One staff as assigned. Study-specific delegated tasks will be determined by the Principal Investigator (if applicable) cons المزيد...

The Lead Site/Study Coordinator supports an assigned group of medical institutions for activities involving clinical trial conduct. Support for staff on protocol-specific tasks will be determined by the Principal Investigator considering all local and federal laws and regulations and 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.Hybrid in Kyiv UkraineThe scope of responsibilities will include:Supervised responsibility for troubleshooting المزيد...

Join our international team and be the key support to clinical research projects streamlining communication maintaining systems and managing documents & information.This role is based in Athens GreeceCommunication and Site ManagementExchanges data documents and other project relev المزيد...

This role supports our Business Development team in building and expanding the sites network as well promotes and supports attracting new projects for Milestone One.In this role you will Build and sustain long-lasting relationships with Investigators and Medical In المزيد...

Start your career in clinical research streamlining communication maintaining systems and managing documents.The scope of responsibilities will include:Maintenance of databases and tracking systemsWork with large amount of documents including their compiling procurement processin المزيد...

The Site Administrator is an integral part of the SEO Operations team and supports the daily operations of clinical trials by assisting in data collection/entry patient interactions (i.e. scheduling and patient flow) and compliance with study protocols. Study-specific delegated tasks 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.Office-based in ZagrebYour role:Prepare clinical t المزيد...

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).Suppor المزيد...

Business Development Representative supports our Business Development team in building and expanding the Milestone One network by identifying and supporting new site partners.   In this role you will:Build and sustain long-lasting relationships with Investigat المزيد...

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 المزيد...

The Lead Site Coordinator supports an assigned group of medical institutions within a geographical area for activities involving clinical trial conduct. Support for staff on protocol-specific tasks will be determined by the Principal Investigator considering all local and federal laws المزيد...

The Site Administrator is an integral part of the SEO Operations team and supports the daily operations of clinical trials by assisting in data collection/entry patient interactions (i.e. scheduling and patient flow) and compliance with study protocols. Study-specific delegated tasks المزيد...

The Site Coordinator supports a medical institution in clinical trial-related activities. Protocol-specific tasks will be determined by the Principal Investigator considering all local and federal laws and regulations and upon review of competencies observed and documented by Mileston المزيد...

Join our international team and be the key support to clinical research projects part of the start-up team working in a dynamic multi-functional environment gaining unique skills from various disciplines relevant to clinical research.This is a hybrid work arrangement that combines wor المزيد...

 Coordinates investigator/ site feasibility and identification process as well as study startup.Monitors project timelines and patient enrollment implements respective corrective and preventive measures.Reviews monitoring visit reports for all visit types and ensures reporting co المزيد...

The Regional Project Lead 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 project team on a country and regional level.Ensures plann المزيد...

The Lead Data Manager is responsible for all data management activities in assigned clinical trials under supervision.Acts as primary communication point for project teams and company departments regarding clinical data managementActs as primary communication point for clients/vendors المزيد...

As a Lead Project Manager your role will consist of two parts: Project Management and Corporate/Departmental Assignments. Project Management responsibilities include:Management of small (<5 countries and/or limited services) and medium sized (5-15 countries and/or full service المزيد...