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Clinical Research Associate II
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Clinical Research Assistant
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Montreal, Quebec, Canada Innovaderm Full timeAbout the RoleWe are looking for a highly motivated and detail-oriented Clinical Research Assistant to join our team at Innovaderm. As a Clinical Research Assistant, you will provide support to our clinical research coordinators during visits to research subjects.Key ResponsibilitiesSupport clinical research coordinators during research patient visits,...
Clinical Research Assistant
2 months ago
About the Role
The Clinical Research Assistant will work under the supervision of Dr. Imran Ahmad and in collaboration with Dr. Jean Roy, holder of the Maryse and William Brock Chair for Clinical Research in Hematopoietic Cell Transplantation at the University of Montreal. This position will be part of the Research Unit in Hematopoietic Cell Transplantation and Cell Therapy.
Main Responsibilities
- Assess the feasibility of future clinical trials
- Collaborate with researchers to develop clinical research protocols
- Review and adapt information and consent forms for new studies and amendments according to local standards
- Coordinate and manage 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 clinical trial implementation
- Conduct budget evaluations for clinical trials and ensure financial follow-up for clinical trials under their responsibility
- Collaborate with the legal team to review agreements
- Analyze collected data during retrospective or prospective studies, perform statistical analyses, and present data in table and graph formats
- 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 performed in accordance with research protocols, applicable regulations, good clinical practices, and standardized operating procedures to achieve the highest standards of quality
- Collaborate with unit members, site personnel, pharmaceutical companies, and contract research organizations (CROs)
- Participate in project meetings to maintain high standards of quality
