Postuler

Publié il y a 18 jours

Senior Clinical Research Associate

@ PSI CRO

Toronto, Ontario

120k–150k $/anTélétravailTemps plein
Postuler
SIGNAUX

En bref

PSI CRO is hiring a freelance Senior Clinical Research Associate in Canada to conduct onsite monitoring visits and manage study sites for clinical trials. The role requires independent monitoring experience in Phase II and/or III studies, with travel and a valid driver's licence. PSI states it does not sponsor work visas.

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 for vendors
  • 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 onsite monitoring experience
  • Experience in all monitoring visit types in Phase II and/or III
  • Full working English proficiency
  • 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
2026-10-23
Première détection par notre source
2026-10-23
Mise à jour du dossier source
2026-10-23

Ces dates décrivent le dossier source, pas une vérification en direct du recrutement. Consultez l’offre originale.

Détails du poste

NiveauSenior
DomaineProfessions paramédicales
Heures par semaine40 (estimé)
Déplacementsroute : modérés
Milieu de travailChez les clients, Bureau
PositionAssis et debout
Exigences physiquesphysique faible · ordinateur élevé
LanguesEnglish
Permis de conduireexigé
FormationBaccalauréat (exigé)
Domaines d’étudesLife 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…

ChampValeur
SecteurPharmaceutical Manufacturing
Taille1,001-5,000 employees
Siège socialZug
Type d’organisationPrivately Held
SpécialitésNumber One Patient Enrollment CROClinical ResearchClinical TrialsOncologyHematologyMultiple SclerosisInfectious DiseasesPatient EnrollmentPhase 2 Phase 3
Offres sur Jobsy7
LinkedInVoir la page
Description

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 3,000 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them.

Job Description

We are looking for an experienced freelance Sr. CRA to support us with the following responsibilities in Canada:

  • 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.
  • 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

For this position, PSI is not hiring individuals who require work visa sponsorship for employment now or in the future.

This is a great opportunity for you to further develop your skills, widen your therapeutic area experience, and become an expert in clinical research.

Emplois semblables

  • Clinical Research Associate II (GTA)

    Oakville, ON
    81k–131k $/anTélétravailTemps plein

    AbbVie

    2+ ansCandidates need at least 2 years of clinically related monitoring experience, including on-site monitoring of investigational drug or device trials. They also need in-depth knowledge of GCP, ICH guidelines and clinical research regulations, plus strong organization and communication skills.

    Microsoft Outlook, Microsoft PowerPoint, Microsoft Excel, Microsoft Word

    Clinical Research Associate II

    Toronto, ON
    81k–131k $/anTélétravailTemps plein

    AbbVie

    2+ ansCandidates need at least 2 years of clinical monitoring experience, including on-site monitoring of investigational drug or device trials. They need in-depth knowledge of clinical research regulations and ICH/GCP guidelines, strong organizational and communication skills, and comfort with Microsoft Office and technology.

    Microsoft Outlook, Microsoft PowerPoint, Microsoft Excel, Microsoft Word

  • Sr. Clinical Research Associate

    Mississauga, ON
    86k–136k $/an

    Novo Nordisk

    5+ ansCandidates need a bachelor's degree in life sciences or a related field and 5+ years of CRA experience. They must know ICH-GCP, use clinical trial systems such as EDC, CTMS and eTMF, and be able to travel up to 70% of the time.

    EDC, CTMS, eTMF

  • Senior Clinical Research Associate

    Burlington, ON
    TélétravailTemps plein

    ICR Canada - CAN

    Candidates need a bachelor's degree in a scientific or healthcare field and extensive CRA experience, including current oncology monitoring. They must manage several sites at once, know clinical trial software, and communicate well with stakeholders.

    Clinical trial software

    Senior Clinical Research Associate

    Burlington, ON +3
    Sur placeTemps plein

    ICR Canada - CAN

    1+ ansCandidates need a bachelor's degree or equivalent in a scientific or health field, or a licensed health professional background such as a registered nurse. They need 1+ years of clinical monitoring experience for level 2, or 3+ years for level 3, plus bilingual English and French.

    Clinical research, Clinical trials, Google Cloud, Bilingualism, English, French

    Senior Clinical Research Associate

    Montréal, QC +1
    Sur placeTemps plein

    ICR Canada - CAN

    3+ ansICON Canada needs a bachelor's degree or equivalent, 3+ years of clinical monitoring experience for level 3, and knowledge of ICH and regulatory rules for drug trials. Bilingual English and French is required, and 70% travel is expected.

    Clinical research, Clinical trials, Google Cloud, Bilingualism, English, French

    Senior Clinical Research Associate

    Burlington, ON +3
    Sur placeTemps plein

    ICR Canada - CAN

    3+ ansCandidates need a bachelor's degree or equivalent in a scientific or health field, plus at least 3 years of clinical monitoring experience for this senior level. Knowledge of ICH and regulatory rules for drug trials and fluent English and French are required.

    Clinical research, Clinical trials, Google Cloud, Bilingualism, English, French

  • Clinical Research Associate

    Ottawa, ON
    80k–85k $/anContrat, Temporaire

    adecco

    2+ ansCandidates need at least 2 years of experience conducting clinical studies and knowledge of clinical research regulations and quality standards. A science bachelor's degree is preferred, and experience with medical devices, diagnostics or Veeva TMF is an asset. Candidates must be legally eligible to work and reside in Canada.

    Veeva

Lieux et modes de travail

Lieux

Tout le CanadaTélétravail · Hybride · Sur place · Sur le terrain

Astuce : ajoutez le télétravail pour élargir la recherche.

Exclure des lieux

Mode de travail

Offres de cette entreprise dans les résultats

Voici les offres de cette entreprise chargées dans votre recherche. Elle peut avoir d’autres postes ouverts.