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Site Management Associate (Japanese Skill required)
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 Management Associate
Summary:
Join our international team and be the key support to clinical research projects, streamlining communication, maintaining systems and managing documents & information. Only CVs in English will be accepted. Hybrid position in Mexico City. You will be responsible for: Being the main point of contact bEmployment Type: Full-time
Experience Level: Entry Level
Medical Monitor (Gastroenterology)
Summary:
As part of PSI's Medical Monitoring team, you will join our international group of medical professionals, build a career on the frontline of medical science and use your knowledge and expertise to help bring new medications to patients that need them. Full-time employment based in Bangkok ResponsibiEmployment Type: Full-time
Experience Level: Associate
Tags: Research Pharmaceuticals
Medical Monitor (Gastroenterology)
Summary:
As part of PSI's Medical Monitoring team, you will join our international group of medical professionals, build a career on the frontline of medical science and use your knowledge and expertise to help bring new medications to patients that need them. Full-time employment, Office location: Tokyo orEmployment Type: Full-time
Experience Level: Associate
Tags: Research Pharmaceuticals
Medical Monitor (Gastroenterology)
Summary:
As part of PSI's Medical Monitoring team, you will join our international group of medical professionals, build a career on the frontline of medical science and use your knowledge and expertise to help bring new medications to patients that need them. Full-time employment based in Singapore ResponsiEmployment Type: Full-time
Experience Level: Associate
Tags: Research Pharmaceuticals
Medical Monitor (Gastroenterology)
Summary:
As part of PSI's Medical Monitoring team, you will join our international group of medical professionals, build a career on the frontline of medical science and use your knowledge and expertise to help bring new medications to patients that need them. Full-time employment based in Australia ResponsiEmployment Type: Full-time
Experience Level: Associate
Tags: Research Pharmaceuticals
Medical Monitor (Gastroenterology)
Summary:
As part of PSI's Medical Monitoring team, you will join our international group of medical professionals, build a career on the frontline of medical science and use your knowledge and expertise to help bring new medications to patients that need them. Full-time employment based in Seoul ResponsibiliEmployment Type: Full-time
Experience Level: Associate
Tags: Research Pharmaceuticals
Medical Monitor (Gastroenterology)
Summary:
As part of PSI's Medical Monitoring team, you will join our international group of medical professionals, build a career on the frontline of medical science and use your knowledge and expertise to help bring new medications to patients that need them. Full-time employment based in Taipei ResponsibilEmployment Type: Full-time
Experience Level: Associate
Tags: Research Pharmaceuticals
Medical Monitor (Gastroenterology)
Summary:
As part of PSI's Medical Monitoring team, you will join our international group of medical professionals, build a career on the frontline of medical science and use your knowledge and expertise to help bring new medications to patients that need them. Full-time employment based in Hong Kong ResponsiEmployment Type: Full-time
Experience Level: Associate
Tags: Research Pharmaceuticals
Medical Monitor (Gastroenterology)
Summary:
As part of PSI's Medical Monitoring team, you will join our international group of medical professionals, build a career on the frontline of medical science and use your knowledge and expertise to help bring new medications to patients that need them. Please provide your CV in English ResponsibilitiEmployment Type: Full-time
Experience Level: Mid-Senior Level
Medical Monitor (Gastroenterology)
Summary:
As part of PSI's Medical Monitoring team, you will join our international group of medical professionals, build a career on the frontline of medical science and use your knowledge and expertise to help bring new medications to patients that need them. Full-time employment based in Malaysia ResponsibEmployment Type: Full-time
Experience Level: Mid-Senior Level
Tags: Other Pharmaceuticals
Data Manager for Clinical Trials
Summary:
Clincial Data Manager plays a critical role in the clinical research project. If you are detail-oriented and committed to quality, able to work with large volume of clinical or medical data, you might be the professional we are looking for. Please submit your CV in English Responsibilities will inclEmployment Type: Full-time
Experience Level: Associate
Tags: Analyst Pharmaceuticals
Study Startup Specialist I
Summary:
Take your career to the next level and be involved in study startup processes in Türkiye. You will provide direct operational support to project teams and ensure that PSI clinical projects start smoothly and on time. Office-Based in Ankara You will: Support site identification and selection processEmployment Type: Full-time
Experience Level: Associate
Tags: Other Pharmaceuticals
Site Management Associate I
Summary:
Join our international team and be the key support to clinical research projects, streamlining communication, maintaining systems and managing documents & information. Office-based in Munich/Planegg The scope of responsibilities will include: Maintenance of databases and tracking systems Work with lEmployment Type: Full-time
Experience Level: Entry Level
Senior Clinical Site Coordinator
Summary:
Please submit CV in English. The Milestone One Senior Clinical Site Coordinator is a key member of the Operations team, taking hands-on responsibility for the preparation, activation, and day-to-day coordination of clinical trial activities at Milestone One-supported investigator sites in Argentina,Employment Type: Full-time
Experience Level: Associate
Medical Reviewer
Summary:
We are seeking a detail-oriented and analytical Medical Reviewer to join our team in Zagreb, Croatia. In this role, you will be responsible for reviewing and evaluating medical content, ensuring accuracy, consistency, and compliance with regulatory standards. Conduct medical review of clinical databEmployment Type: Full-time
Experience Level: Associate
Tags: Other Pharmaceuticals
Events Manager
Summary:
As Events Manager you will oversee the planning and execution of international meetings - from coordinating logistics and managing vendors to supporting budgets, travel, compliance, and post‑event processes. You’ll ensure smooth, well‑organized events and serve as a key partner to internal teams andEmployment Type: Full-time
Experience Level: Mid-Senior Level
Tags: Other Pharmaceuticals
Regulatory Officer (Clinical Trial Submissions)
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 in Kazakhstan, while taking a step further in your professional career. Office-based in Almaty You will: Prepare clinical trialEmployment Type: Full-time
Experience Level: Associate
Tags: Other Pharmaceuticals
Regulatory Affairs Assistant
Summary:
Join our international team and support regulatory aspects of clinical research projects, streamlining communication, maintaining electronic systems and managing documents. Full-time employment based in Almaty, Kazakhstan You will: Be the point of contact for clinical project teams and support serviEmployment Type: Full-time
Experience Level: Associate
Tags: Other Pharmaceuticals
Clinical Regional Project Lead
Summary:
In this role you will streamline activities of project teams in China and ensure consistency of Clinical Operations processes across regions. You will ensure meeting study milestones by project teams on a country level, report study progress to clients and global stakeholders. The scope of responsibEmployment Type: Full-time
Experience Level: Mid-Senior Level
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
Site Management Associate II
Summary:
Start your career in clinical research, streamlining communication, maintaining systems and managing documents. The scope of responsibilities will include: Main site contact for all non-trial-participant related and non-protocol related issues, including vendors, trial supplies and access managementEmployment Type: Full-time
Experience Level: Entry Level