Support clinical project teams from a home-based setting through document control, meeting coordination, and stakeholder communications. Keep project information organized, tracked, and aligned.
This Clinical Project Coordinator provides administrative, clerical, implementation, and processing support across project activities. The work includes document management, reporting, training coordination, billing support, and responding to project queries. Success requires clinical research knowledge, communication skills, independent work, and cross-functional collaboration.
Key Responsibilities:
- Manage and maintain project materials, tools, equipment, and supplies
- Track, update, revise, distribute, and record project activity
- Prepare forms, logs, reports, scripts, and project documents
- Support issue identification and resolution during audits
- Ensure activities follow protocols, standards, and regulatory guidelines
Requirements:
- One to three years of related work experience with training
- Relevant one-year college advanced diploma or degree
- Health, life sciences, or clinical research education preferred
- Knowledge of clinical research and strong communication skills
- Ability to work independently and cross-functionally
Apply clinical research knowledge and organized document control skills to support compliant project delivery from your home-based setting.
Clinical Project Coordinator Document Control in Kitchener employer: Alimentiv
At Alimentiv, we pride ourselves on being a purpose-driven employer that invests in our people and their professional growth. Our collaborative work culture fosters innovation and accountability, while our comprehensive benefits, including education reimbursement and mentorship programs, ensure that you feel valued and supported in your career journey. Join us in advancing therapies for gastrointestinal diseases and be part of a team that is dedicated to making a meaningful impact in the lives of patients worldwide.
