Summary
Overview
Work History
Education
Skills
Additional Information
Timeline
Generic

Razieh (Rose) Alemi

Montreal,CA

Summary

  • Canadian/Iranian Headline
  • Highly motivated and detail-oriented Trilingual Clinical Research Coordinator (CRC) with 10+ Years of experience in research and clinics and a strong academic background in Neuroscience seeking a Clinical Research Associate role.
  • Eager to apply theoretical knowledge, enthusiasm for research, and commitment to learning in a professional setting at Worldwide Clinical Trials. Professional Summary
  • Multicenter/multinational experienced Clinical Research Coordinator and Postdoctoral Research Fellow with over 10 years of expertise in clinical studies, neuroscience, and pharmaceutical research (gene expression).
  • Proficient in conducting diverse clinical trials (observational), overseeing research protocols, and ensuring regulatory compliance.
  • Proven leadership in mentoring research staff, strong analytical thinking, and expertise in managing behavioral studies, genetic lab techniques, and participant recruitment strategies.
  • Strong understanding of research methodologies, data analysis, and scientific principles gained through academic coursework.
  • Proficiency in Microsoft Office Suite and familiarity with data management and statistical analysis software.
  • Excellent communication and interpersonal skills developed through group projects, presentations, or extracurricular activities.
  • Detail-oriented with a commitment to accuracy and maintaining organized records.
  • Independent and quick learner with a strong desire to gain hands-on experience in pharmaceutical-related clinical research.
  • Proficient in effectively prioritizing workloads across various studies to consistently meet project timelines and deliverables.
  • Comprehensive expertise in the methodology governing the execution and oversight of clinical research per ICH-GCP guidelines.
  • Recognized reviewer by prestigious publishers, demonstrating a commitment to scientific rigor and excellence.

Overview

9
9
years of professional experience

Work History

Clinical Research Coordinator/Postdoctoral Research Fellow

Concordia University
Montreal, QC
04.2021 - Current
  • Crafting research protocols and relevant literature reviews
  • Performing ethics applications for IRB/REB approval and designing informed consent forms and advertisements
  • Contributing to research team meetings, offering insights and suggestions based on academic knowledge
  • Leading and coordinating clinical research efforts, overseeing multiple studies involving psychoacoustic, EEG, and fNIRS techniques
  • Mentoring and guiding research staff, ensuring adherence to regulatory protocols, and fostering an efficient research environment
  • Utilizing analytical skills to assist in interpreting research data and findings
  • Reviewing research data and maintaining study-related databases
  • Writing scientific papers and reports and overseeing relevant communications (e.g., rebuttal letters, ongoing modifications, and amendments).

Clinical Research Coordinator/Postdoctoral Research Fellow

Otolaryngology, McGill University
Montreal, QC
01.2019 - 03.2021
  • Developing comprehensive research protocols and conducting in-depth literature reviews relevant to the field
  • Conducting ethics applications for IRB/REB approval, designing informed consent forms and advertisements, and effectively presenting research protocols to the Centre for Interdisciplinary Research in Rehabilitation of Greater Montreal (CRIR) REB for review and approval
  • Executing participant recruitment strategies, managing communications, and ensuring high retention rates
  • Engaging in patient communication (particularly with Francophone individuals), conducting screenings, and efficiently scheduling test dates
  • Reviewing patient charts and research data and contacting relevant clinics to update the data registry
  • Conducting observational trials and behavioral studies, contributing to publications in renowned scientific journals
  • Assisting clinical research teams with administrative tasks, such as organizing documents and maintaining files
  • Demonstrating commitment and enthusiasm for learning about clinical research methodologies and practices

Researcher, team member

Neuroimaging and Analysis Group, Imam Khomeini Hospital Complex, Tehran University of Medical Sciences
, Tehran
02.2015 - 04.2016
  • Collaborating in crafting protocols funded by the Iranian Cognitive Sciences and Technologies Council
  • Spearheaded a study aimed at identifying brain regions involved in sentence comprehension, semantics, and speech production to provide a template for neurosurgeons
  • Designing three distinct fMRI tasks targeting eloquent brain areas critical to language function investigation
  • Participant recruitment (72 participants): Performing training sessions for each individual to ensure optimal task performance during brain scans
  • Analyzing individual datasets, ensuring quality control for each file
  • Assisting the biostatistician in analyzing group-level data
  • Crafting manuscripts (Journal publication) and reports for submission to the council
  • Managing the submission process, including preparing rebuttal letters and addressing queries
  • Collaborating with team members in scanning participants for two other tasks related to memory function
  • Contributing to literature reviews and manuscript writing.

Education

Ph.D - Neuroscience

School of Advanced Technologies in Medicine, Tehran University of Medical Sciences
March 2018

M.Sc. - undefined

University of Social Welfare and Rehabilitation Sciences
Sep 2008

B.Sc. - undefined

Tehran University of Medical Sciences
July 2005

Master of Science - Speech and Language Pathology

Bachelor of Science - Speech and Language Pathology

<ul><li>IDAA))</li><li>Clinical Research Professional Certification</li></ul> - undefined

Skills

  • Technical Skills
  • Clinical research management
  • GCP compliance
  • Data management and statistical analysis (fMRI, EEG, fNIRS)
  • Genetic lab techniques
  • Participant recruitment strategies
  • Research protocol development
  • IRB/REB documentation
  • Areas of Expertise
  • Clinical trial (observational) oversight and management
  • Behavioral and observational studies
  • Regulatory compliance and ethics approval
  • Multidisciplinary team leadership
  • Scientific writing and publication (demonstrated by a track record of published papers)

Additional Information

  • CRA school, Montreal (2023-Ongoing) Awards/Certifications Horizon Post-Doctoral Research Award (Sponsored by Concordia University) MITACS Post-Doctoral Research Award (Sponsored by Med-El company in collaboration with McGill University) Travel Awards for European Symposiums on Pediatric Cochlear Implant (2013, 2015, 2019) Holding the certificate of Tri-Council Policy Statement 2: Core

Timeline

Clinical Research Coordinator/Postdoctoral Research Fellow

Concordia University
04.2021 - Current

Clinical Research Coordinator/Postdoctoral Research Fellow

Otolaryngology, McGill University
01.2019 - 03.2021

Researcher, team member

Neuroimaging and Analysis Group, Imam Khomeini Hospital Complex, Tehran University of Medical Sciences
02.2015 - 04.2016

Ph.D - Neuroscience

School of Advanced Technologies in Medicine, Tehran University of Medical Sciences

M.Sc. - undefined

University of Social Welfare and Rehabilitation Sciences

B.Sc. - undefined

Tehran University of Medical Sciences

Master of Science - Speech and Language Pathology

Bachelor of Science - Speech and Language Pathology

<ul><li>IDAA))</li><li>Clinical Research Professional Certification</li></ul> - undefined

Razieh (Rose) Alemi