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…
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Description complète de l’entreprise
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
Abonnés LinkedIn
329 384
Personnes associées sur LinkedIn
2 861
Bureaux déclarés
Baarerstrasse 113a, Zug, 6300, CH
Catégories d’activité
Business Information Systems
Health Care
Pharmaceutical
Autres noms enregistrés
PSI CRO
Spécialités
Number One Patient Enrollment CRO
Clinical Research
Clinical Trials
Oncology
Hematology
Multiple Sclerosis
Infectious Diseases
Patient Enrollment
Phase 2
Phase 3
Pivotal Trials
Global Clinical Trials
Full-Service Clinical Trials
and Radiopharmaceuticals
Le profil indique une agence de recrutement
Non
Investissement total déclaré
0
La devise et la date d’observation ne sont pas fournies; ce n’est ni une valorisation actuelle ni une ronde de financement.
Secteur
Pharmaceutical Manufacturing
Taille
1,001-5,000 employees
Siège social
Zug
Type d’organisation
Privately Held
Spécialités
Number One Patient Enrollment CROClinical ResearchClinical TrialsOncologyHematologyMultiple SclerosisInfectious DiseasesPatient EnrollmentPhase 2 Phase 3
PSI CRO a 7 offres ouvertes au Canada en date du 9 novembre 2026. Principaux lieux : Calgary, Vancouver et Toronto.
5+ ansCandidates need a life sciences degree or equivalent, 5+ years of independent on-site monitoring experience across phases I-III, and independent oncology and IBD trial experience. They must live on Canada's West Coast, travel up to 75%, and hold a valid driver's licence.
Candidates need a university degree in Life Sciences or equivalent experience, independent onsite monitoring experience in North America, and experience with Phase II or III monitoring visits. Full working proficiency in English and French and travel ability are also required.
10+ ansCandidates need a medical degree and Canada board certification in psychiatry, plus at least 10 years of practicing psychiatry. Clinical research experience is preferred, along with strong communication and analytical skills.
Candidates need a college or university degree in life sciences or equivalent experience, plus independent onsite monitoring experience in Phase II and/or III trials. Full English proficiency, MS Office skills, travel ability and a valid driver's licence are required.
2+ ansCandidates need a college or university degree or equivalent experience, at least two years in clinical research, and prior experience negotiating site budgets. Knowledge of clinical trial legal documents and medical terminology is a plus.
Negotiation, Clinical research, Medical terminology
10+ ansCandidates need an MD, Canada board certification in gastroenterology, and at least 10 years of practicing gastroenterology. Clinical research experience, MS Office skills, and strong communication and analytical abilities are preferred.
Candidates need a life sciences degree or equivalent experience, independent onsite monitoring experience in Phase II or III studies, and full working proficiency in English and French. Travel and a valid driver's licence are required.