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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
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. As an in-house translator, you will be expected to: TranslateEmployment Type: Full-time
Experience Level: Associate
Clinical Trial Liaison
Summary:
As part of the PSI team, you will have a fair degree of ownership and autonomy to make nuanced country-and department-specific adjustments while nurturing the global PSI culture that unites us across six continents. You will: Act as a specialized liaison to assist sites with a protocol-tailored apprEmployment Type: Full-time
Experience Level: Mid-Senior Level
Tags: Other Pharmaceuticals
Country Approval Specialist / 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. Office-based role in Ra'anana , Israel You will: Prepare clinical triEmployment Type: Full-time
Experience Level: Not Applicable
Junior IT Systems Administrator
Summary:
RESPONSIBILITIES 1.1. Supervised responsibility for troubleshooting and diagnosing desktop computer systems and peripheral equipment problems 1.2. Supervised responsibility for IT support operations, including but not limited to receiving and tracking user requests, assigning priority and responsiblEmployment Type: Full-time
Experience Level: Mid-Senior Level
HR Development Partner
Summary:
The Global HR Development Partner will collaborate closely with the Global HR Manager to design and implement key HR initiatives across all regions. This role focuses on employee assessment, leadership capability building, training program design, and providing regional HR expertise to ensure compliEmployment Type: Full-time
Experience Level: Associate
Tags: Research 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
Study Startup Specialist I/II
Summary:
Take your career to the next level and lead challenging study activation process on a country/regional level. You will support clinical research teams and ensure PSI projects start smoothly and on time. Office based in Taipei You will: Maintains study-specific and corporate startup tracking systemsEmployment Type: Full-time
Experience Level: Associate
Tags: Other Pharmaceuticals
Office Manager
Summary:
SCOPE OF RESPONSIBILITIES 1. Office Management 1.1. Responsible for new office site selection, decoration, vendor management and etc. 1.2. Coordinates the purchase and inventory of office supplies 1.3. Oversees office maintenance and management of the office vendors to ensure smooth operation of theEmployment Type: Full-time
Experience Level: Mid-Senior Level
Full-stack Developer (AI Solutions)
Summary:
We're looking for a full stack developer to join our growing Process Improvement team. If you're interested in AI solutions development and would like to further enhance your engineering skillset in a global company, then PSI might be the right choice for you. Full-time employment based in Spain YouEmployment Type: Full-time
Experience Level: Associate
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
Clinical Trial Liaison (Operating Room Nurse)
Summary:
We are looking for an Operating Room (OR) Nurse to join PSI as a Clinical Trial Liaison! In this role, a Clinical Trial Liaison: Acts as a specialized liaison to assist sites with a protocol-tailored approach to increase efficiency of the patient identification and recruitment process Assists sitesEmployment Type: Full-time
Experience Level: Mid-Senior Level
Tags: Other Pharmaceuticals
Site Management Associate (内勤モニター)
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
Study Startup / Site Activation Specialist - Temporary position
Summary:
Take your career to the next level and lead challenging study activation process on a country level. You will support clinical research teams and ensure PSI projects start smoothly and on time. You will mainly: Lead finalization of site/vendor agreements and budgets negotiation to ensure alignment tEmployment Type: Full-time
Experience Level: Associate
Tags: Other Pharmaceuticals
Submission Specialist / 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. Office-based role in Ra'anana , Israel You will: Prepare clinical triEmployment Type: Full-time
Experience Level: Not Applicable
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
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: Conduct and report all types of onsite monitoring visits Be involved in study sEmployment Type: Full-time
Experience Level: Associate
Tags: Research Pharmaceuticals
Principal Lead Data Manager
Summary:
Acts as primary communication point for project teams and company departments regarding clinical data management. Acts as primary communication point for clients/vendors for all data management aspects of clinical projects and clinical data management reporting. Responsible for the supervision of alEmployment Type: Full-time
Experience Level: Mid-Senior Level
Tags: Other Pharmaceuticals
Principal Lead Data Manager
Summary:
Acts as primary communication point for project teams and company departments regarding clinical data management. Acts as primary communication point for clients/vendors for all data management aspects of clinical projects and clinical data management reporting. Responsible for the supervision of alEmployment Type: Full-time
Experience Level: Mid-Senior Level
Tags: Other Pharmaceuticals
Clinical Trials Business Development Representative (Freelance)
Summary:
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). Support Site Development ManageEmployment Type: Contract
Experience Level: Mid-Senior Level
Tags: Research 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