Montreal Clinical Trial Associate: TMF

Overview Abich Inc. Canada is a leading provider of research, clinical, and analytical services, supporting the cosmetic, personal care, medical devices, and natural health industries. With over 10 years of expertise, we assist clients throughout their product's lifecycle, from initial formulation to market release. Our team leverages innovative technologies...

Overview Abich Inc. Canada is a leading provider of research, clinical, and analytical services, supporting the cosmetic, personal care, medical devices, and natural health industries. With over 10 years of expertise, we assist clients throughout their product's lifecycle, from initial formulation to market release. Our team leverages innovative technologies...

A leading research service provider in Montreal is seeking a Clinical Trial Associate for a full-time on-site position. You will support the planning, execution, and coordination of clinical trials while ensuring regulatory compliance. Key responsibilities include managing Informed Consent processes and updating the Trial Master File. The ideal candidate...

Company DescriptionAbich Inc. Canada is a leading provider of research, clinical, and analytical services, supporting the cosmetic, personal care, medical devices, and natural health industries. With over 10 years of expertise, we assist clients throughout their product's lifecycle, from initial formulation to market release. Our team leverages innovative...

A clinical research organization is seeking a professional to manage the Trial Master File (TMF) content throughout the study lifecycle. The successful candidate will ensure TMF completeness and readiness for inspection while providing primary support for assigned studies. They will need 3-5 years of TMF oversight experience and a solid understanding of TMF...

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...

Base pay range CA$52,500.00/yr - CA$87,500.00/yr Responsible for the management of the Trial Master File (TMF) content and associated processes during the study life cycle from study setup to transfer/archiving. Work in partnership with study teams during periodic file reviews and audits to address findings related to the TMF. Manage access and organization...

A leading pharmaceutical company in Montreal is seeking a Quality Control Associate to ensure data compliance during clinical trials. The successful candidate will oversee data quality, report trends, and maintain participant files. Requirements include a DEC, bilingual proficiency in French and English, and knowledge of Good Clinical Practices. This on-site...

A leading clinical research organization in Montreal is seeking an Associate in quality control of participant selection tests for clinical trials. The role involves performing quality control on data collected, ensuring compliance with protocols, and identifying trends. Candidates should have a DEC, be bilingual in French and English, and possess strong...

A leading clinical research organization in Montreal is seeking an Associate in quality control of participant selection tests for clinical trials. The role involves performing quality control on data collected, ensuring compliance with protocols, and identifying trends. Candidates should have a DEC, be bilingual in French and English, and possess strong...