Publié il y a 29 jours
Medical Monitor (Canada Board-Certified Gastroenterologist)
@ PSI CRO
Télétravail au Canada
En bref
PSI CRO is hiring a Medical Monitor, a full-time, home-based role in Canada for a board-certified gastroenterologist. The role provides medical and safety input to global clinical studies, advising trial teams while protecting patient safety. The posting requires an MD, Canada board certification in gastroenterology and at least 10 years of practice.
Responsabilités :
- Serve as primary medical contact on trial safety questions
- Monitor trial participant safety
- Review SAE narratives, RAE reports and IND/SUSAR safety reports
- Train trial teams on therapeutic area and protocol medical aspects
- Review clinical study reports and protocol deviations
Résumé des exigences :
- MD degree required
- Canada board certification in gastroenterology required
- Minimum 10 years of practicing gastroenterology
- Clinical research experience preferred
- Proficiency with MS Office applications
Outils et compétences
Source et dates
Site carrière / système de candidatures · smartrecruiters
- Date publiée par l’employeur
- 2026-10-14
- Première détection par notre source
- 2026-10-14
- Mise à jour du dossier source
- 2026-10-14
Ces dates décrivent le dossier source, pas une vérification en direct du recrutement. Consultez l’offre originale.
Détails du poste
| Niveau | Senior |
| Domaine | Médecins et pratique avancée |
| Expérience | 10 an(s) et plus |
| Heures par semaine | 40 (estimé) |
| Déplacements | avion : aucun · route : aucun |
| Milieu de travail | Domicile |
| Position | Surtout assis |
| Exigences physiques | physique faible · ordinateur élevé |
| Langues | English |
| Permis et certifications | Canada Board Certification in Gastroenterology |
| Formation | Diplôme professionnel (médecine, droit…) (exigé) |
| Domaines d’études | Medicine |
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 more than 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
PSI Medical Monitors provide medical input to global clinical studies and advise the teams and business partners, while always focusing on patients' safety and well-being.
Home-Based in Canada
Responsibilities:
- Acts as the primary point of contact for all parties on all trial-specific medical and safety-related questions
- Provides input for responses to regulatory authorities and Institutional Review Boards (IRBs)/Independent Ethics Committees (IECs) on trial-specific medical and safety-related questions
- Monitors trial participant safety
- Participates in trial participant recruitment boost and retention activities
- Presents on medical matters at kick-off and investigator meetings
- Trains trial team in the therapeutic area and medical aspects of the protocol
- Develops and reviews trial-specific documents within the scope of medical monitoring
- Manages ongoing trial risks related to medical monitoring
- Performs ongoing medical review of the operational clinical trial database; provides support to Medical Reviewer(s) assigned to the trial
- Reviews protocol deviations
- Reviews RAE reports, writes and/or reviews SAE narratives, supports Pharmacovigilance team with outstanding safety queries, interacts with sponsor on site safety issues
- Reviews IND/SUSAR Safety Reports, updates/amendments to essential trial records, and annual IND reports with sponsor data (per sponsor request)
- Participates in management of trial-related committees (e.g., independent data monitoring committee (IDMC)/adjudication committees) as described in the corresponding trial-specific charter(s)
- Supports Pharmacovigilance, Medical Data Review and Data Management with reconciliation of safety and operational clinical trial databases
- Reviews clinical study reports (CSRs), including safety narratives and tables, figures, and listings (TFLs)
- Provides medical expertise on an as-needed basis in trials where medical monitoring is not a contract deliverable
- Prepares for and participates in trial audits, follows up on audit findings
- Participates in feasibility assessment of potential and ongoing trials in the country/region
- Participates in bid defense meetings and other interactions with clients
- Acts as a medical expert and provides therapeutic expertise to other PSI departments
Qualifications
- Medical Doctor degree required
- Canada Board Certification in Gastroenterology required
- Experience as a practicing Gastroenterology (minimum of 10 years)
- Clinical Research experience preferred
- Proficiency with MS Office applications
- Communication, presentation and analytical skills
- Problem-solving, team and detail-oriented
Additional Information
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.
Journal
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