Razieh Alemi Email & Phone Number

Canada

Montreal, Quebec, Canada

• Assisting with protocol and grant preparations for funding organizations.
• Preparing applications for central REB (Nagano) and Health Canada (including Évaluations des facteurs relatifs à la vie privée (EFVP) amendments).
• Preparing the site for monitoring visits and audits.
• Serving as the main point of contact for site-related queries.
• Managing and monitoring the conduct of clinical trials at the site level.
• Supervising the recruitment and screening of study participants.

Montreal, Quebec, Canada

• Acquired and maintained a strong understanding of Health Canada and FDA regulations.
• Monitored site compliance with protocol and FDA, HC & ICH-GCP.
• Maintaining appropriate documentation for IRB applications.
• Reviewing protocols, drafted protocol summary and NDA for PI recruitment (oncology: renal cell carcinoma; metabolic: obesity).
• Developed feasibility questionnaire, IB (endocrine), and lists of activities for monitoring visits.
• Implemented and verified subject recruitment SOPs and study- related documents (different therapeutic areas).

(Loyola Campus) Montreal, Quebec, Canada

• Spearheaded the development of research protocols and conducted literature reviews, contributing to the team's success.
• Ensured adherence to SOPs in project management and execution, resulting in enhanced project efficiency.
• Facilitated the approval process by preparing ethics applications for IRB/REB submission.
• Accelerated study startup activities, resulting in shortened timelines and created error-reducing manuals for research staff.
• Achieved high participant retention rates through effective management of recruitment efforts.
• Efficiently trained and supervised research staff, ensuring timely completion of tasks and adherence to protocols.

(Glen site/MUHC) Montreal, Quebec, Canada

• Led the development of research protocols.
• Completed ethics applications for IRB/REB approval, ensuring compliance with regulatory requirements.
• Implemented effective participant recruitment strategies, resulting in consistently high retention rates throughout the studies.
• Conducted observational trials and behavioral studies, generating valuable insights into patient behavior and treatment outcomes.
• Proactively engaged with patients, conducted screenings, and scheduled test dates, optimizing study enrollment processes.
• Reviewed patient charts and research data meticulously, ensuring data accuracy and completeness for analysis.

Montreal, Quebec, Canada

Montreal, Quebec, Canada

Tehran Province, Iran

• Collaborated in crafting protocols for a neuro-oncology trial to perform personalized-based surgery treatment for patients with brain tumors using fMRI and DTI techniques.
• Attended different meetings to design fMRI tasks to provide templates for neurosurgeons (tumor resection surgery).
• Scanned 80 participants (including the pilot study) and trained individuals before fMRI sessions to ensure optimal performance.
• Collaborated with another colleague to perform DTI (side study).
• Analyzed individual datasets and performed quality control for each dataset.
• Assisted the biostatistician with group-level data analysis.

Doctor Of Philosophy - Phd, Neuroscience

Master'S Degree, Speech-Language Pathology/Pathologist

Bachelor'S Degree, Speech-Language Pathology/Pathologist

Clinical Research Professional Certification, Clinical Research Associate