Piedmont Healthcare Inc.

Piedmont Healthcare Inc.

Clinical Trial Associate 2

Canada, Burlington · Contract

Sponsorship not specifiedDetected 7 days ago
AccessibilityPLCClinical TrialsClinical ResearchResearchCommunicationCollaborationProblem Solving

About the role

  • Your Profile: You will have a strong foundation in clinical trial management, with the experience to work independently and guide others.
  • Vos responsabilités Vous assumerez la responsabilité de plusieurs livrables liés à la gestion des essais cliniques, en mettant à profit votre expertise pour relever des défis complexes et contribuer au succès des projets.
  • Votre profil Vous possédez une solide expérience en soutien à la gestion des essais cliniques et êtes capable de travailler de façon autonome tout en accompagnant et en guidant vos collègues lorsque nécessaire.

Responsibilities

  • Providing administrative support for clinical trials, including managing documentation, coordinating meetings, and maintaining trial-related records.
  • Assisting in the preparation and submission of regulatory documents and ensuring compliance with study protocols and regulatory requirements.
  • Collaborating with cross-functional teams to support trial operations and resolve any issues that arise during the course of the study.
  • Building and maintaining strong relationships with site staff and other stakeholders to facilitate smooth trial operations and support overall project success.
  • Extensive experience in a clinical trial support role, with a solid understanding of clinical trial processes and regulatory requirements.
  • Strong organizational and multitasking skills, with the ability to manage multiple tasks and projects effectively.
  • Participer à la préparation et à la soumission des documents réglementaires, tout en veillant au respect des protocoles d'étude et des exigences réglementaires applicables.
  • We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.

Requirements

  • Proficiency in clinical trial management systems and relevant software, with a keen eye for detail in documentation and data management.
  • Excellent communication, interpersonal, and problem-solving skills, with the ability to work collaboratively with diverse teams and stakeholders.
  • Willingness to travel as required (approximately 10%)
  • Diplôme universitaire (Licence/Bachelor ou équivalent) dans une discipline scientifique pertinente ou un domaine lié à la santé.

Compensation

  • Competitive base salary and performance related incentives

Benefits

  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training and career pathways
  • Visit our careers site to read more about the benefits ICON offers.
  • Bachelor's degree in a relevant scientific discipline or healthcare-related field

Equal opportunity

  • ICON is an equal opportunity employer.

This listing is sourced directly from Piedmont Healthcare Inc.'s careers page and normalized into a canonical job model.