Alireza Minagar, MD, MBA, MS (Bioinformatics)
Neurologist, Neuro-immunologist
Bioinformatics Scientist/AI/ML
Cell number: 318-***-****
Email address: ********@*****.***
LinkedIn profile: https://www.linkedin.com/in/alireza-minagar-md-mba-ms-biotech-bioinformatics-b450aa173/
Clinical Trialist, and Principal Medical Writer with expertise in Data Analysis. Proficient in SQL, Python, and Java programming, as well as Artificial Intelligence and Machine Learning.
December 2023: I finished the post Graduate Program in Artificial Intelligence and Machine Learning: Business Applications at Univ. Texas at Austin, TX, USA
Currently, I am engaged as an independent medical writing consultant and pharmaceutical consultant. During the period from 2020 to the present, I have had the privilege of collaborating with esteemed clients, including:
University of Maryland
Biogen
Seattle Genetics
Wolters Kluwer
Presently, attending Artificial Intelligence course via Great Learning/Univ. Texas-Austin (pending graduation)
Objective: Highly accomplished Neurologist and Neuro-Immunologist with over 23 years of experience in the healthcare and pharmaceutical industry. Expert in clinical trial management, medical writing, and data analysis, with strong proficiency in SQL, Python, Java, Artificial Intelligence, and Machine Learning. Seeking to leverage extensive background in neuroscience and biotechnology to drive innovation and excellence in clinical research and pharmacovigilance.
Professional Experience:
Professor of Neurology LSU Health Sciences Center - Shreveport Dec 2001 – Oct 2020
Led academic and clinical research in neurology and neuro-immunology.
Developed and implemented neuroscience curriculum, emphasizing clinical applications.
Principal Investigator for numerous clinical trials, ensuring compliance with GCP and SOPs.
Managed interdisciplinary teams and coordinated with pharmaceutical companies.
Director of Clinical Operations LSU HSC-Shreveport 6 years
Oversaw clinical trial operations, including planning, execution, and compliance.
Coordinated with cross-functional teams for seamless trial management.
Implemented quality management systems to enhance clinical operations.
Clinical Trialist / Clinical Trial Manager LSU HSC-Shreveport 16 years
Managed Phase I-III clinical trials, focusing on neurological disorders.
Ensured regulatory compliance and liaised with internal and external stakeholders.
Developed risk management strategies to ensure patient safety and pharmacovigilance.
Principal Medical Writer LSU HSC-Shreveport 6 years
Authored a wide range of medical and regulatory documents, including CSRs, IBs, and RMPs.
Represented the organization in client meetings and medical conferences.
Mentored junior medical writers, ensuring high-quality content development.
Training Medical Science Liaison (MSL) personnel for pharmaceutical companies:
Coordinated scientific collaboration in neurology and psychiatry
Oversaw the entire product lifecycle from Business Development to implementation.
Collaborated across departments in US.
Delivered medical training for teams and speakers.
Provided clinical support to Healthcare Providers (HCPs), addressed inquiries, and identified opportunities.
Participated in regional symposia, advisory boards, and medical meetings.
Kept abreast of scientific developments through active conference participation.
Shared medical information at exhibit booths during conferences.
Contributed to major projects, initiatives, and leadership within the team.
Education:
Master of Biotechnology (Bioinformatics) University of Maryland Global Campus, 2021-2023
Post Graduate Program in Artificial Intelligence and Machine Learning: Business Applications at Univ. Texas at Austin, TX, USA 2023
Java Programmer & Python Developer Program Louisiana State University - Shreveport, 2021-2022
Master of Business Administration (MBA) Louisiana State University, Shreveport, 2015-2017
Fellowship in Clinical Neuro-Immunology / Multiple Sclerosis Multiple Sclerosis Center of University of Miami, 1999-2001
Neurology Residency University of Miami, 1997-1999; New York University, 1996-1997
Internal Medicine Mount Vernon Hospital Mt. Vernon, NY 1995-1996
MD Tehran University of Medical Sciences, 1984-1991
Certifications and Skills:
Certifications: Java and Python programmer and developer
Skills: Clinical Trials Management, Medical Writing, Data Analysis, Regulatory Compliance, SQL, Python, Java, Artificial Intelligence, Machine Learning
Advanced International Pharmacovigilance and Argus Safety Certification (APVASC)
By CCRPS-2024
Professional Development:
Currently enrolled in a course on Artificial Intelligence and Machine Learning, University of Texas at Austin.
Regular participant and speaker at national and international scientific congresses.
Reviewer for grant applications - NIH and Italian MS society.
Additional Skills:
10-11 years of Continuing Medical Education (CME) experience in reputable institutions and pharmaceutical companies, including LSUHSC-Shreveport, Biogen.
Proficient in Microsoft Office Suite for creating educational materials.
Built strong relationships with key opinion leaders in CME initiatives.
Proven ability to manage multiple priorities with meticulous attention to detail.
Strong interpersonal and communication skills for positive interactions at all organizational levels.
Creative thinker consistently generating new ideas to enhance educational content.
Enthusiastic team player with a positive attitude, fostering effective collaboration.
Therapeutic Area and Disease Experience:
Extensive experience in multiple sclerosis, Alzheimer's Disease, stroke, and cerebrovascular diseases.
Over 6 years of expertise in oncology and 12 years each in psychiatry (including schizophrenia, mood disorders) and neuro-ophthalmology.
Proficient in the management and clinical trials of treatments like Alferon-N (Interferon AN3) and interventions for conditions such as Persian Gulf Syndrome, reduced cardiac ejection fraction, and insulin resistance post-stroke.
Skilled in bioinformatics, monoclonal antibodies, biostatistics, artificial intelligence, and machine learning.
Related Skills and Experience:
Proficient medical writer with experience in creating Investigator’s Brochures, Informed Consent Forms, and other regulatory documents.
Served as Principal Investigator and Clinical Scientist, contributing significantly to pharmacovigilance and IRB submissions.
Expertise in needs assessment, clinical study report (CSR) preparation, FDA Form 1572, Master Clinical Trial Agreements, study protocols, Pediatric Investigation Plans (PIPs), Clinical Trial Applications (INDs, CTAs), and Marketing Applications (NDAs, BLAs, MAAs), along with CMC Information Amendments.
Publications and Contributions:
Scientific Articles in Peer-Reviewed Journals
284 Articles in Peer Reviewed Journals, List available on request.
PubMed Link: https://pubmed.ncbi.nlm.nih.gov/?term=Minagar+A+
Abstracts (88 Abstracts, List available on request).