Taipei, Taiwan · On-site
Company Description PSI is a leading Contract Research Organization (CRO) with 30 years of experience in the pharmaceutical industry. Originated in Switzerland, PSI is a privately owned, full-service CRO with a global re…
Skills: Medical Monitoring, Gastroenterology, Clinical Research, Pharmacovigilance, Clinical Development Plans
Taipei, Taiwan · On-site
Company Description PSI is a leading Contract Research Organization (CRO) with 30 years of experience in the pharmaceutical industry. Originated in Switzerland, PSI is a privately owned, full-service CRO with a global re…
Skills: Medical Monitoring, Clinical Research, Pharmacovigilance, Clinical Development Planning, Regulatory Compliance
Seoul, South Korea · On-site
Company Description PSI is a leading Contract Research Organization (CRO) with 30 years of experience in the pharmaceutical industry. Originated in Switzerland, PSI is a privately owned, full-service CRO with a global re…
Skills: Medical Monitoring, Gastroenterology, Clinical Research, Pharmacovigilance, Clinical Development Plans
Seoul, South Korea · On-site
Company Description PSI is a leading Contract Research Organization (CRO) with 30 years of experience in the pharmaceutical industry. Originated in Switzerland, PSI is a privately owned, full-service CRO with a global re…
Skills: Medical Monitoring, Clinical Research, Pharmacovigilance, Clinical Development Planning, Regulatory Compliance
Seoul, South Korea · On-site
Company Description PSI is a leading Contract Research Organization (CRO) with 30 years of experience in the pharmaceutical industry. Originated in Switzerland, PSI is a privately owned, full-service CRO with a global re…
Skills: Medical Monitoring, Clinical Research, Pharmacovigilance, Clinical Development Planning, Regulatory Compliance
Sydney, New South Wales, Australia · On-site
Company Description PSI is a leading Contract Research Organization (CRO) with 30 years of experience in the pharmaceutical industry. Originated in Switzerland, PSI is a privately owned, full-service CRO with a global re…
Skills: Medical Monitoring, Gastroenterology, Clinical Research, Pharmacovigilance, Clinical Development Plans
Sydney, New South Wales, Australia · On-site
Company Description PSI is a leading Contract Research Organization (CRO) with 30 years of experience in the pharmaceutical industry. Originated in Switzerland, PSI is a privately owned, full-service CRO with a global re…
Skills: Medical Monitoring, Clinical Research, Pharmacovigilance, Clinical Development Planning, Protocol Development
Durham, North Carolina, United States · On-site
Company Description We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together more 3,000 driven, …
Skills: Clinical Research, Document Management, Regulatory Submissions, TMF Management, EDC
Kuala Lumpur, Kuala Lumpur, Malaysia · On-site
Company Description We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together more than 3,000 dri…
Skills: Operational Strategies, Clinical Trials, Site Identification, Market Trends, Stakeholder Relationships
Leuven, Flanders, Belgium · On-site
Company Description We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together more 3,000 driven, …
Skills: Administrative Work, Communication, Document Management, Database Maintenance, Organizational Skills
United States · Hybrid
Company Description We are a fast-growing Site Enabling Organization operating globally in the field of clinical research. We are driven by quality, teamwork, and innovation. As we continue to expand our global operation…
Skills: Clinical Trial Management, Patient Recruitment, GCP Compliance, EDC Systems, Phlebotomy
United States · Hybrid
Company Description We are a fast-growing Site Enabling Organization operating globally in the field of clinical research. We are driven by quality, teamwork, and innovation. As we continue to expand our global operation…
Skills: Clinical Trial Management, Patient Recruitment, GCP Compliance, EDC/EMR Systems, Phlebotomy
United States · Hybrid
Company Description We are a fast-growing Site Enabling Organization operating globally in the field of clinical research. We are driven by quality, teamwork, and innovation. As we continue to expand our global operation…
Skills: Clinical Trial Management, Patient Recruitment, GCP Compliance, EDC Systems, Phlebotomy
Milan, Lombardy, Italy · On-site
$28k–$41k/yr
Company Description We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together more than 3000 driv…
Skills: Database Maintenance, Document Management, Clinical Research, Communication, Project Coordination
United States · Remote Solely
Company Description PSI is a leading Contract Research Organization with more than 30 years in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on deliveri…
Skills: Medical Monitoring, Patient Safety, Clinical Trial Management, Pharmacovigilance, Regulatory Compliance
Buenos Aires, Argentina · Remote Solely
Company Description PSI is a leading Contract Research Organization with more than 30 years in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on deliveri…
Skills: Medical Monitoring, Patient Safety, Clinical Trial Management, Pharmacovigilance, Regulatory Compliance
São Paulo, São Paulo, Brazil · Remote Solely
Company Description PSI is a leading Contract Research Organization with more than 30 years in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on deliveri…
Skills: Medical Monitoring, Patient Safety, Clinical Trial Management, Pharmacovigilance, Regulatory Compliance
Warsaw, Masovian Voivodeship, Poland · Hybrid
Company Description Why PSI? Because we are not a huge corporation and people still matter here. Our managers and employees have autonomy in making decisions and creating an engaging work environment. We provide the oper…
Skills: On-site Monitoring, Study Startup, CRF Review, Source Document Verification, Query Resolution
Warsaw, Masovian Voivodeship, Poland · Hybrid
Company Description Why PSI? Because we are not a huge corporation and people still matter here. Our managers and employees have autonomy in making decisions and creating an engaging work environment. We provide the oper…
Skills: On-site Monitoring, Study Startup, CRF Review, Source Document Verification, Query Resolution
Tallinn, Estonia · On-site
Company Description We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together more than 3,000 dri…
Skills: Expense Management, Financial Analysis, Accounting, Document Management, MS Excel
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Provide medical expertise to clients and project teams to ensure the safety of study participants and the accuracy of clinical data. Collaborate on the preparation of clinical development plans, protocols, and regulatory documents while managing program risks.
Requires a Medical Doctor degree with preferred board-certification in Gastroenterology and prior experience in clinical research. Candidates must be proficient in local regulations, ICH/GCP guidelines, and possess strong leadership and communication skills.
PSI is a leading Contract Research Organization (CRO) with 30 years of experience in the pharmaceutical industry. Originated in Switzerland, PSI is a privately owned, full-service CRO with a global reach, supporting clinical trials across multiple countries and continents. Our reputation for being highly selective about the projects we undertake highlights our commitment to delivering high-quality, timely services across a broad spectrum of therapeutic indications.
At PSI, we foster an environment where a diverse range of colleagues feel welcomed and valued. Our inclusive culture is a cornerstone of our success, enabling us to attract and retain top talent globally.
We are not just about conducting clinical trials; we are about building a community where every team member has the opportunity to thrive and contribute to groundbreaking advancements in the pharmaceutical industry.
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.
Join our highly dedicated team of clinical research professionals with 250+ Medical Doctors onboard, and make a tangible difference within a professional and energetic organization founded by scientists.
PSI is a leading full-service global Contract Research Organization whose key strength is predictable patient enrollment across multiple therapeutic areas. PSI is known in the industry as a CRO focused on ‘on-time project delivery’. This is achieved through investing substantial effort and MD resources into performing quality feasibility assessments that provide an accurate predictor of study timelines. PSI’s global reach allows us to run clinical trials across multiple continents, in 50+ countries around the world. PSI’s reputation is that of a 'no-nonsense' CRO focused on timely patient enrollment and project delivery. An exceptionally high repeat and referral business rates alongside low staff turnover are indicative of our commitment to be the best CRO in the world as measured by our clients and our employees. http://www.psi-cro.com
Offices: Baarerstrasse 113a, Zug, 6300, CH
PSI is a leading full-service global Contract Research Organization whose key strength is predictable patient enrollment across multiple therapeutic areas. PSI is known in the industry as a CRO focused on ‘on-time project delivery’. This is achieved through investing substantial effort and MD resources into performing quality feasibility assessments that provide an accurate predictor of study timelines. PSI’s global reach allows us to run clinical trials across multiple continents, in 50+ countries around the world. PSI’s reputation is that of a 'no-nonsense' CRO focused on timely patient enrollment and project delivery. An exceptionally high repeat and referral business rates alongside low staff turnover are indicative of our commitment to be the best CRO in the world as measured by our clients and our employees. http://www.psi-cro.com
Offices: Baarerstrasse 113a, Zug, 6300, CH
