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Senior Clinical Research Associate
Summary:
As a Senior CRA 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. Office-based/Hybrid in Seoul, South Korea Responsibilities Prepare, conduct, and report site selection, inEmployment Type: Full-time
Experience Level: Associate
Tags: Other Pharmaceuticals
Document Specialist
Summary:
If you are keen to provide administrative, document management support to pharmaceutical research projects, and be involved in something new, outstanding and challenging, this job opportunity is perfect for you! The scope of responsibilities will include: Review, maintain and archive essential studyEmployment Type: Full-time
Experience Level: Entry Level
Regulatory Officer
Summary:
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, Romania Your role: Prepare cEmployment Type: Full-time
Experience Level: Associate
Tags: Other Pharmaceuticals
Site Management Associate
Summary:
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, Greece Communication and Site Management Exchanges data, documents and other project relevant informatEmployment Type: Full-time
Experience Level: Associate
Senior Workday Lead
Summary:
Hybrid work in Bucharest The Workday HCM Senior Lead will serve as the internal system owner and strategic lead for Workday HCM and Core Compensation, acting as the primary liaison between internal stakeholders and external Workday consultants. This role is responsible for overseeing post go-live stEmployment Type: Full-time
Experience Level: Associate
Senior Workday Lead
Summary:
Hybrid work in Oxford The Workday HCM Senior Lead will serve as the internal system owner and strategic lead for Workday HCM and Core Compensation, acting as the primary liaison between internal stakeholders and external Workday consultants. This role is responsible for overseeing post go-live stabiEmployment Type: Full-time
Experience Level: Associate
Senior Workday Lead
Summary:
Hybrid work in Sofia The Workday HCM Senior Lead will serve as the internal system owner and strategic lead for Workday HCM and Core Compensation, acting as the primary liaison between internal stakeholders and external Workday consultants. This role is responsible for overseeing post go-live stabilEmployment Type: Full-time
Experience Level: Associate
Senior Workday Lead
Summary:
Hybrid work in Madrid The Workday HCM Senior Lead will serve as the internal system owner and strategic lead for Workday HCM and Core Compensation, acting as the primary liaison between internal stakeholders and external Workday consultants. This role is responsible for overseeing post go-live stabiEmployment Type: Full-time
Experience Level: Associate
Clinical Research Associate
Summary:
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. Full-time office-based in Tbilisi, Georgia You will: Conduct and report all types of onsEmployment Type: Full-time
Experience Level: Associate
Tags: Research Pharmaceuticals
Clinical Regional Project Lead
Summary:
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 planning, implementEmployment Type: Full-time
Experience Level: Mid-Senior Level
Tags: Management Pharmaceuticals
Clinical Regional Project Lead
Summary:
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 planning, implementEmployment Type: Full-time
Experience Level: Mid-Senior Level
Tags: Management Pharmaceuticals
Clinical Regional Project Lead
Summary:
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 planning, implementEmployment Type: Full-time
Experience Level: Mid-Senior Level
Tags: Management Pharmaceuticals
Clinical Regional Project Lead
Summary:
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 planning, implementEmployment Type: Full-time
Experience Level: Mid-Senior Level
Tags: Management Pharmaceuticals
Clinical Regional Project Lead
Summary:
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 planning, implementEmployment Type: Full-time
Experience Level: Mid-Senior Level
Tags: Management Pharmaceuticals
Site Identification Specialist (Feasibility)
Summary:
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. This is a home-based position in Slovakia. General Responsibilities: Maintain and refine internal siEmployment Type: Full-time
Experience Level: Associate
Tags: Other Pharmaceuticals
Site Identification Specialist (Feasibility)
Summary:
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. General Responsibilities: Maintain and refine internal site databases in cooperation with Study StarEmployment Type: Full-time
Experience Level: Associate
Tags: Other Pharmaceuticals
Site Contract Specialist I
Summary:
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- and site-specific agreements and orgaEmployment Type: Full-time
Experience Level: Associate
Tags: Research Pharmaceuticals
Site Contract Specialist I
Summary:
The Site Contract Specialist can be based anywhere in Canada. 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- and site-specific agreements and organizing theiEmployment Type: Full-time
Experience Level: Associate
Tags: Research Pharmaceuticals
Study Startup Specialist I
Summary:
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. Home-based in Canada You will: Supports all processes critical for site activation.Employment Type: Full-time
Experience Level: Associate
Clinical Research Associate II
Summary:
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, sponsor, and thEmployment Type: Full-time
Experience Level: Associate
Tags: Research Pharmaceuticals
Clinical Research Associate II
Summary:
If you are currently a CRA I looking forward to the next step of your career, this might be the right position for you! 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 qualEmployment Type: Full-time
Experience Level: Mid-Senior Level
Tags: Research Pharmaceuticals
Lead Clinical Research Associate
Summary:
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 compliance of the MEmployment Type: Full-time
Experience Level: Mid-Senior Level
Tags: Management Pharmaceuticals