At a Glance
- Tasks: Manage Trial Master File processes and ensure compliance throughout the study lifecycle.
- Company: Leading clinical research organization in Canada with a focus on innovation.
- Benefits: Flexible remote work, competitive salary, and opportunities for professional growth.
- Other info: Enjoy a supportive work environment with occasional office visits.
- Why this job: Join a dynamic team and contribute to impactful clinical research projects.
- Qualifications: College diploma and 1-3 years of experience in TMF organization and compliance.
The predicted salary is between 50067 - 61193 $ per year.
A leading clinical research organization in Canada is seeking a TMF Coordinator to manage Trial Master File processes throughout the study lifecycle.
The ideal candidate will have a college diploma and 1-3 years of relevant experience, emphasizing TMF organization and regulatory compliance.
Responsibilities include ensuring the TMF is complete and ready for inspection, providing training, and maintaining quality assurance standards.
This full-time role offers the flexibility to work from home with occasional office visits. #J-18808-Ljbffr
TMF Compliance Associate – Remote in Montréal 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.
