Clinical Research Assistant
5 days ago
About the Role
The Clinical Research Assistant will work under the supervision of Dr. Imran Ahmad and the responsibility of Dr. Jean Roy, holder of the Maryse and William Brock Chair for Clinical Research in Hematopoietic Cell Transplantation at the University of Montreal. The successful candidate will work in the Research Unit in Hematopoietic Cell Transplantation and Cell Therapy. In collaboration with hematologists and research unit members, this person will participate at various levels in the feasibility, setup, conduct, and closure of clinical trials in hematopoietic cell transplantation and cell therapy, primarily initiated by local researchers. Their work and activities must be carried out in accordance with research protocols, hospital procedures, good clinical practices, and applicable regulations.
Main Responsibilities
- Participate in the evaluation of the feasibility of future clinical trials
- Collaborate in the writing of clinical research protocols initiated by local researchers
- Review and adapt new study information and consent forms in accordance with local standards
- Set up and conduct clinical trials to ensure their smooth execution
- Complete, review, and maintain regulatory and ethical documents for clinical trials
- Prepare documents for ethics and regulatory submissions and contribute to obtaining the required approvals from various committees for the setup of clinical trials
- Evaluate the budget of clinical trials and ensure financial follow-up of clinical trials under their responsibility
- Collaborate with the legal team for the review of agreements
- Verify collected data during retrospective or prospective studies, perform statistical analyses, and present data in the form of tables and graphs
- Assist in writing and submitting scientific articles and abstracts
- Collaborate in submitting grant applications to funding agencies and pharmaceutical companies for studies initiated by local researchers
- Ensure effective communication with sponsors and partners and respond to their requests
- Collaborate with unit members, research administration, and institutional services to ensure the smooth operation of ongoing studies
- Ensure that work is carried out in accordance with protocols, applicable regulations, good clinical practices, and standardized operating procedures to achieve the highest quality standards
- Collaborate with unit members, site personnel, pharmaceutical companies, and research contract organizations (CRO)
- Participate in project meetings to maintain high-quality standards
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