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Clinical Research Coordinator

@ ClinSurge Research

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Nepean, Ontario

Temps plein
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En bref

ClinSurge Research is hiring a full-time Clinical Research Coordinator to manage and coordinate clinical research studies under Good Clinical Practice, institutional guidelines and federal regulations. The role covers participant recruitment, consent, data collection, regulatory documentation and adverse event reporting, on-site in a physician practice and clinical research setting. The posting requires a bachelor's degree in a health or life science field and states that phlebotomy certification is required, with preferred experience of 1-3 years.

Responsabilités :

  • Coordinate and conduct clinical research studies, including recruitment, consent and follow-up
  • Ensure compliance with protocols and Health Canada, IRB and ICH-GCP requirements
  • Collect and enter data into EDC systems
  • Maintain regulatory binders, subject files and case report forms
  • Monitor and report adverse events and prepare for monitoring visits and audits

Résumé des exigences :

  • Bachelor's degree in health sciences, life sciences, nursing or related field (required)
  • 1-3 years clinical research experience (preferred)
  • CCRC or CCRP certification (asset)
  • Phlebotomy certification and IATA shipping knowledge
  • Strong knowledge of GCP, Health Canada and IRB regulations
  • Proficiency with EDC systems and Microsoft Office

Outils et compétences

MedidataRAVEMicrosoft Officeelectronic data capture (EDC) systems
Source et dates

Site carrière / système de candidatures · jazzhr

Date publiée par l’employeur
2026-09-13
Première détection par notre source
2026-10-09
Mise à jour du dossier source
2026-10-16

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

Détails du poste

NiveauDébutant
DomaineProfessions paramédicales
Heures par semaine40 (estimé)
Déplacementsavion : aucun · route : aucun
Milieu de travailHôpital ou clinique, Laboratoire, Bureau
PositionAssis et debout
Exigences physiquesphysique faible · ordinateur élevé
Permis et certificationsPhlebotomy certification, CCRC, CCRP
FormationBaccalauréat (exigé)
Domaines d’étudeshealth sciences, life sciences, nursing

Résumé et détails rédigés par l’IA à partir de l’offre; l’offre de l’employeur fait foi.

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ClinSurge Research

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Description complète de l’entreprise

At ClinSurge Research, we are dedicated to transforming healthcare through innovative clinical research.

Abonnés LinkedIn
2 565
Personnes associées sur LinkedIn
18
Autres noms enregistrés
  • ClinSurge Research
Le profil indique une agence de recrutement
Non
Toutes ses offres Site Web

At ClinSurge Research, we are dedicated to transforming healthcare through innovative clinical research.

ChampValeur
SecteurResearch Services
Taille11-50 employees
Type d’organisationPrivately Held
Fondée en2025
Offres sur Jobsy5
LinkedInVoir la page
Description

Position Summary:

We are seeking a motivated and detail-oriented Clinical Research Coordinator (CRC) to manage and coordinate clinical research studies in accordance with Good Clinical Practice (GCP), institutional guidelines, and federal regulations. The CRC will work closely with investigators, sponsors, and participants to ensure the integrity of study protocols and data collection.

Key Responsibilities:

  • Coordinate and conduct all aspects of clinical research studies, including participant recruitment, consent, scheduling, and follow-up.
  • Ensure compliance with study protocols and regulatory requirements (Health Canada, IRB, ICH-GCP).
  • Collect and enter data accurately into electronic data capture (EDC) systems.
  • Maintain study documents, including electronic regulatory binders, subject files, and case report forms.
  • Monitor and report adverse events and ensure timely communication with the IRB and sponsors.
  • Prepare for and participate in monitoring visits, audits, and inspections.
  • Collaborate with cross-functional teams, including principal investigators, sponsors, and other research personnel.

Qualifications:

  • Bachelor’s degree in health sciences, life sciences, nursing, or a related field (required).
  • Minimum [1-3] years of experience in clinical research (preferred).
  • Certified Clinical Research Coordinator (CCRC) or Certified Clinical Research Professional (CCRP) a plus.
  • Phlebotomy certification and proficiency in drawing with ability to process and ship per IATA requirements.
  • Strong knowledge of GCP, Health Canada, and IRB regulations.
  • Excellent organizational, communication, and problem-solving skills.
  • Proficiency with EDC systems (e.g., Medidata, or RAVE) and Microsoft Office Suite.

Work Environment:

  • On-site in physician practice and clinical research setting.
  • May require handling of biological samples and/or working with patients.

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