Munich, Bavaria, Germany · On-site
Company Description We are the company that cares – for our staff, for our clients, for our partners and for the quality of work we do. A dynamic, global company founded in 1995, we bring together more than 2,700 driven,…
Skills: Biostatistics, Clinical trials, SAS programming, Statistical analysis, CDISC ADaM
Toronto, Ontario, Canada · On-site
Company Description We are the company that cares – for our staff, for our clients, for our partners and for the quality of work we do. A dynamic, global company founded in 1995, we bring together more than 2,700 driven,…
Skills: Biostatistics, Clinical trials, SAS programming, Statistical analysis, Protocol development
Saint-Maur-des-Fossés, Ile-de-France, France · On-site
Company Description We are the company that cares – for our staff, for our clients, for our partners and for the quality of work we do. A dynamic, global company founded in 1995, we bring together more than 2,700 driven,…
Skills: Biostatistics, Clinical trials, SAS programming, Statistical analysis, Protocol development
Lima, Lima, Peru · On-site
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: Pharmacovigilance, Clinical research, Data entry, Safety reporting, Japanese language
Buenos Aires, Argentina · On-site
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: Pharmacovigilance, Clinical research, Data entry, Safety reporting, Japanese language
São Paulo, São Paulo, Brazil · On-site
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: Pharmacovigilance, Clinical research, Data entry, Safety reporting, Japanese language
Bogotá, Bogota D.C., Colombia · 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 2,800 dri…
Skills: Clinical research, Clinical trial administration, Document management, Regulatory compliance, CTMS
Santiago, Santiago Metropolitan Region, Chile · 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 2,800 dri…
Skills: Clinical research, Clinical trial management, Document management, Regulatory compliance, Site management
King of Prussia, Pennsylvania, 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 than 2,800 dri…
Skills: Desktop Support, Troubleshooting, Hardware Maintenance, Software Configuration, Asset Management
Skopje, North Macedonia · 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, mid-size company founded in 1995, we bring together more than…
Skills: Clinical Research Associate, Monitoring Visits, CRF Review, Source Document Verification, Query Resolution
King of Prussia, Pennsylvania, 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 than 3,000 dri…
Skills: Clinical operations, Clinical trials, Administrative support, Regulatory submissions, Ethics committee submissions
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 than 3,000 dri…
Skills: Clinical operations, Clinical trials, Administrative support, Regulatory submissions, Ethics committee submissions
Tokyo, Japan · On-site
Company Description PSI is a leading full-service global Contract Research Organization providing a wide range of clinical trial services to the pharmaceutical and biotechnology industry, mainly for the development of cl…
Skills: Contract Drafting, Contract Negotiation, Legal Advice, Compliance, Legal Research
Toronto, Ontario, Canada · On-site
$124k–$153k/yr
Company Description PSI is a leading Contract Research Organization with more 30 years in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering qu…
Skills: Site Monitoring, Clinical Trial Management, Oncology, Regulatory Compliance, Project Coordination
United States · Remote OK
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: On-site Monitoring, Source Data Verification, Clinical Trial Management, Oncology, Gastrointestinal Research
United States · Remote OK
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 2,800 dri…
Skills: Onsite Monitoring, CRF Review, Source Document Verification, Site Management, Quality Control
West Coast Division, The Gambia · Remote OK
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 2,800 dri…
Skills: Clinical research, Onsite monitoring, Oncology, Site management, Source document verification
Ciudad de México, Mexico · 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 2,500 dri…
Skills: Clinical Monitoring, CRF Review, Source Document Verification, Site Management, Query Resolution
Tallinn, Estonia · 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: Graphic Design, Visual Communications, Event Production, Presentation Design, Adobe InDesign
Tbilisi, Georgia · 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: Graphic Design, Visual Communications, Event Production, Presentation Design, Adobe InDesign
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Lead biostatistics activities for clinical trials, including protocol development, statistical analysis plans, and SAS programming. Collaborate with project teams, clients, and vendors to ensure high-quality statistical deliverables and regulatory compliance.
Requires an MSc in Statistics or equivalent with expert knowledge of clinical research statistical principles and SAS programming. Must possess strong experience with CDISC ADaM standards and relevant regulatory guidelines like FDA and EMA.
We are the company that cares – for our staff, for our clients, for our partners and for the quality of work we do. A dynamic, global company founded in 1995, we bring together more than 2,700 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them.
Our mission is to be the best CRO in the world as measured by our employees, clients, sites, and vendors. Our recruitment process is easy and straightforward, and we’ll be there with you every step of the way.
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
