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.
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