Publié il y a 4 heures
Senior Clinical Research Associate
@ PSI CRO
Calgary, Alberta
En bref
PSI CRO is hiring a Senior Clinical Research Associate for full-time work monitoring clinical studies across several therapeutic areas. The role involves onsite monitoring visits, source document verification, site management and audit preparation. The posting requires independent on-site monitoring experience, a life sciences degree or equivalent, full working proficiency in English and French, and the ability to travel.
Salaire :
120 000 $–150 000 $ par année
Responsabilités :
- Conduct SIV, RMV and COV onsite monitoring visits
- Perform CRF review, source document verification and query resolution
- Manage site communication and act as point of contact
- Support regulatory team with study submission documents
- Prepare for and participate in audits and inspections
Résumé des exigences :
- College or university degree in life sciences or equivalent
- Independent on-site monitoring experience in Phase II and/or III
- Oncology experience an asset
- Full working proficiency in English and French
- Valid driver's licence and ability to travel
Outils et compétences
Source et dates
Site carrière / système de candidatures · smartrecruiters
- Date publiée par l’employeur
- 2026-11-10
- Première détection par notre source
- 2026-11-10
- Mise à jour du dossier source
- 2026-11-10
Ces dates décrivent le dossier source, pas une vérification en direct du recrutement. Consultez l’offre originale.
Détails du poste
| Niveau | Senior |
| Domaine | Professions paramédicales |
| Heures par semaine | 40 (estimé) |
| Déplacements | route : modérés |
| Milieu de travail | Chez les clients, Bureau |
| Position | Assis et debout |
| Exigences physiques | physique faible · ordinateur élevé |
| Langues | English, French |
| Permis de conduire | exigé |
| Formation | Baccalauréat (exigé) |
| Domaines d’études | Life Sciences |
Résumé et détails rédigés par l’IA à partir de l’offre; l’offre de l’employeur fait foi.
PSI CRO
Profil d’entreprise sauvegardé
Renseignements historiques provenant d’un profil The Jobs API sauvegardé (champs LinkedIn/Crunchbase). Ils ne sont pas vérifiés en temps réel; les chiffres peuvent avoir changé. Les valeurs manquantes restent inconnues.
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.
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…
| Champ | Valeur |
|---|---|
| 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 |
| Offres sur Jobsy | 7 |
| Voir la page |
Company Description
PSI is a leading Contract Research Organization with 30 years in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications.
Job Description
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 SIV, RMV, COV onsite monitoring visits
- Perform CRF review, source document verification and query resolution
- Be responsible for site communication and management
- Be a point of contact for in-house support services and vendors
- Communicate with internal project teams regarding study progress
- Participate in feasibility research
- Support regulatory team in preparing documents for study submissions
- Prepare and particiapte on audits and inspections
Qualifications
- College/University degree in Life Sciences or an equivalent combination of education, training & experience
- Independent on-site monitoring experience
- Experience in all types of monitoring visits in Phase II and/or III
- Experience in Oncology is a plus
- Full working proficiency in English and French is essential.
- Proficiency in MS Office applications
- Ability to plan, multitask and work in a dynamic team environment
- Communication, collaboration, and problem-solving skills
- Ability to travel
- Valid driver’s license
Additional Information
This is a great opportunity for you to further develop your skills, widen your therapeutic area experience, and become an expert in clinical research.
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