2 meilleures offres (registered nurse, saskatchewan) (à pourvoir)

Principal Investigator
Advanced Care Group —Canada
- À partir de 70 $ de l’heure
- Travail hybride
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Bilingual Field Nurse Case Manager
BioScript Solutions —Canada
- 8 Heures
- Bilingue
- Microsoft Word
- Microsoft Excel
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Principal Investigator
Advanced Care Group —Canada
*Active Registered Nurse (RN) license* in good standing — no lapsed or restricted licenses will be considered. AC Group | Full-Time or Part-Time *.
À partir de 70 $ de l’heure
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Bilingual Field Nurse Case Manager
BioScript Solutions —Canada
Registered Nurse designation and current provincial licensing is required; Attractive Compensation: Competitive salary, incentive program, and comprehensive…
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Je souhaite recevoir la dernière alerte emploi pour les postes de ce type : registered nurse (saskatchewan)

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Principal Investigator

Advanced Care Group
Canada

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Détails du poste

Occasionnel

Compétences

Phlébotomie
Gestion des données
Collecte de données
Terminologie médicale
Marketing

Description complète du poste

Principal Investigator – Clinical Trials (Phase III / IV) | RN
AC Group | Full-Time or Part-Time

About the Role

AC Group partners with leading pharmaceutical and biotech companies to conduct Phase III and Phase IV post-marketing clinical trials. We are actively seeking experienced Registered Nurses to serve as Principal Investigators within our research network. In Phase III and IV studies, an RN PI is fully qualified to lead site-level operations, hold regulatory accountability, and drive protocol execution — and we are built to support you in doing exactly that.

This is a compensated, flexible engagement with FMV-based pay structured around hourly rates, per-patient fees, and per-protocol startup stipends.

What You'll Do

Serve as the named PI on industry-sponsored clinical trial agreements and hold site-level regulatory accountability under Form FDA 1572
Lead all protocol activities at your site in compliance with ICH-GCP E6 R2/R3 and applicable FDA regulations (21 CFR Part 312)
Oversee patient safety monitoring, informed consent processes, and adverse event identification and reporting
Supervise and delegate to study coordinators via a current Delegation Log
Maintain the site Trial Master File (TMF) in inspection-ready condition
Serve as primary point of contact for sponsor/CRO monitoring visits, audits, and data query resolution
Collaborate closely with the AC Group team on site startup, enrollment, and closeout

Required Qualifications — Mandatory

Active Registered Nurse (RN) license in good standing — no lapsed or restricted licenses will be considered
Minimum 2 years of Documented prior experience as a named Principal Investigator or Sub-Investigator on at least one industry-sponsored clinical trial — applicants without hands-on trial site experience will not be reviewed
Current Good Clinical Practice (GCP) certification (ICH E6 R2 or R3) — must be active, current, and submitted with application
All applicable nursing credentials and specialty certifications must be current and in good standing

Preferred Qualifications

Phase III or Phase IV / post-marketing trial experience preferred
ACRP Certified Clinical Research Professional (CCRP) or SOCRA CCRP credential
Experience with EDC platforms (Medidata Rave, REDCap, Veeva Vault)
Oncology, cardiology, neurology, or other specialty nursing background aligned with our active protocol portfolio
Prior Form FDA 1572 signatory experience

Compensation

FMV-based hourly rate based on specialty and experience
Per-patient and per-visit fees per active protocol
Site startup stipend upon protocol activation
Flexible engagement — compatible with existing clinical roles

Apply today [email protected]

Pay: From $70.00 per hour

Application question(s):

Do you have minimum 2 years experience as a PI?

Work Location: Hybrid remote in Canada

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