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Grants Expense Coordinator
Summary:
We are now expanding Operations in the UK and looking for a dynamic and knowledgeable Coordinator to join PSI Grants Expense Management division. 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 clinicEmployment Type: Full-time
Experience Level: Associate
Site Management Associate
Summary:
Join our international team as a key support for clinical research projects. Your responsibilities will include: Maintain databases, tracking systems, and manage large volumes of documents Serve as the primary communication point for investigative sites and internal departments Coordinate site-speciEmployment Type: Full-time
Experience Level: Entry Level
Clinical Site Technology Specialist (Nuclear Medicine)
Summary:
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 technology (Nuclear mEmployment Type: Full-time
Experience Level: Associate
Tags: Other Pharmaceuticals
Clinical Research Associate II
Summary:
As a Clinical Research Associate at PSI you will be involved in improving patients' lives while enjoying a variety of monitoring tasks and working on clinical studies in different therapeutic indications, maintaining the highest quality standards in the industry. Home-based in Portugal You will: ConEmployment Type: Full-time
Experience Level: Associate
Tags: Other Pharmaceuticals
IT Compliance Specialist
Summary:
In this role, you will focus on compliance matters related to in-house IT systems and processes. You will work with documents to make sure that PSI meets standards, industry requirements, and internal policies. Create, update and process internal IT documents (change control, risk assessment, computEmployment Type: Full-time
Experience Level: Associate
IT Systems Administrator
Summary:
We are looking for professional, qualified and enthusiastic candidates to take up a full-time position of an IT Systems Administrator to provide daily technical support in our Munich/Planegg office . The scope of responsibilities will include: Troubleshooting and diagnosing desktop computer systemsEmployment Type: Full-time
Experience Level: Entry Level
IT Compliance Specialist
Summary:
In this role, you will focus on compliance matters related to in-house IT systems and processes. You will work with documents to make sure that PSI meets standards, industry requirements, and internal policies. Create, update and process internal IT documents (change control, risk assessment, computEmployment Type: Full-time
Experience Level: Associate
Site Identification Specialist
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. Hybrid role in Budapest, Hungary This is the main responsibility of a site ID specialist CommunicateEmployment Type: Full-time
Experience Level: Associate
Tags: Other Pharmaceuticals
Site Identification Specialist
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. Hybrid role in Budapest, Hungary This is the main responsibility of a site ID specialist CommunicateEmployment Type: Full-time
Experience Level: Associate
Tags: Other Pharmaceuticals
AI Business Analyst
Summary:
Only CV's in English will be considered Key Responsibilities Become a subject matter expert in all of our internal AI Applications and their capabilities. Apply prompt engineering and prompt engineering frameworks to optimize AI output for different business needs. Create marketing materials, includEmployment Type: Full-time
Experience Level: Associate
Tags: Other Pharmaceuticals
Grants Expense Coordinator
Summary:
We are now expanding Operations and looking for a dynamic and knowledgeable Coordinator to join PSI Grants Expense Management division. Based in Poland In this role, your goal will be to ensure that physicians and hospitals receive on time and accurate payments for their participation in the globalEmployment Type: Full-time
Experience Level: Entry Level
Tags: Analyst Pharmaceuticals
Site Management Associate (Clinical Trial)
Summary:
Join our international team and be the key support to clinical research projects, streamlining communication, maintaining systems and managing documents & information. The scope of responsibilities will include: Maintenance of databases and tracking systems. Serves as the primary sites’ contact poinEmployment Type: Full-time
Experience Level: Entry Level
Document Management Specialist (Clinical Trial)
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
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. The scope of responsibilities will include: Maintenance of databases and tracking systems Serves as the primary sites’ contact pointEmployment Type: Full-time
Experience Level: Entry Level
Site Contract Specialist
Summary:
Join our international team and be the key support to clinical research projects, as part of the start-up team, working in a dynamic multi-functional environment, gaining unique skills from various disciplines relevant to clinical research. This role is hybrid - Based in Budapest You will: CoordinatEmployment Type: Full-time
Experience Level: Associate
Tags: Other Pharmaceuticals
IT Compliance Specialist
Summary:
In this role, you will focus on compliance matters related to in-house IT systems and processes. You will work with documents to make sure that PSI meets standards, industry requirements, and internal policies. Create, update and process internal IT documents (change control, risk assessment, computEmployment Type: Full-time
Experience Level: Associate
Site Management Associate (Japanese Speaking)
Summary:
Join our international team and be the key support to clinical research projects, streamlining communication, maintaining systems and managing documents & information. The scope of responsibilities will include: Maintenance of databases and tracking systems Serves as the primary sites’ contact pointEmployment Type: Full-time
Experience Level: Entry Level
Receptionist / Office Management Coordinator
Summary:
We are looking for a professional, qualified and enthusiastic candidate to take up the full-time position of Receptionist (Office Management Coordinator) to support our well-established PSI Prague office. As the ideal candidate, you have the ability to juggle multiple tasks and act as the voice andEmployment Type: Full-time
Experience Level: Associate
Tags: Other Pharmaceuticals
Translator/Interpreter
Summary:
We're looking for an in-house language professional dedicated to producing high-quality translations, providing interpreting support, and using their skills in an international setting. You might be the language expert we're looking for. This role is hybrid - Based in Budapest As an in-house translaEmployment Type: Full-time
Experience Level: Associate
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
Document Management 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
Site Management Associate (SMA)
Summary:
Join our international team and be the key support to clinical research projects, streamlining communication, maintaining systems and managing documents & information. You will focus on facilitating research projects of novel medicinal products, while taking a step further in your professional careeEmployment Type: Full-time
Experience Level: Entry Level