Afrah Mujeeb
Regulatory Intelligence Project Analyst @ Medtronic
About
Regulatory Affairs Explorer at Northeastern University Hello! I am Afrah Mujeeb, a driven individual currently pursuing a Master's degree in Regulatory Affairs at Northeastern University. My academic journey has equipped me with a comprehensive understanding of global regulatory frameworks, encompassing FDA laws, EU directives, and international standards. With a focus on drugs, biologics, and medical devices, I'm deeply passionate about compliance and ensuring adherence to regulatory standards. Through diverse courses spanning clinical research to quality management systems, I have sharpened my analytical skills and problem-solving abilities. These skills, coupled with my innate leadership qualities, enable me to effectively navigate complex regulatory landscapes and drive projects towards successful outcomes. My academic endeavors have not only enhanced my theoretical knowledge but have also fostered practical skills vital for the field. I have developed strong communication skills through collaborative projects and presentations, while my teamwork abilities have been refined through group assignments and discussions. My goal is to leverage my expertise to contribute to the development of safe and effective healthcare products, collaborating with like-minded professionals who share my dedication to excellence. Please feel free to reach out to me at mujeeb.a@northeastern.edu for any inquiries or discussions. Here's to making health and safety a big win for everyone! #RegulatoryExplorer #HealthHero #ComplianceCrew
United States
Boston
Higher Education
Data Analysis, Institutional Review Board (IRB), Scientific Research Abilities, Adaptability, Flexibility, Submission Preparation, Regulatory Requirements, Risk Assessment and Management, Regulatory Intelligence, Documentation and Record Keeping, Quality Management Systems (QMS), Good Regulatory Practices (GRP), Corrective Actions, Legal Research, Written Communication, Interpretation of Regulations, Policy Analysis, Regulatory Strategy Development, Technical Understanding, Research and Analysis
Experience

Operations Coordinator
Boston, Massachusetts, United States
• Track and manage package deliveries for students and faculty, ensuring accurate and timely distribution. • Enter tracking numbers and dispatch packages to appropriate lockers, maintaining high organizational standards. • Sort and categorize incoming mail and packages by ID for efficient retrieval and distribution. • Maintain a systematic and organized mailroom, enhancing accessibility and workflow. • Enter package and mail information into the database, ensuring precise records and effective tracking. • Assist students and faculty at the front desk with package pickup and mail queries, providing excellent customer service and resolving issues promptly. • Answer front desk phone calls, addressing inquiries and providing information related to package and mail services.

Poster Abstract Screener
United States
• Reviewed and evaluated 30 poster abstracts for approval in diverse fields including regulatory affairs, clinical research, clinical trials, non-clinical studies, in-vitro studies, biopharmaceuticals, and research and development for the 2024 PharmSci 360 conference. • Conducted thorough assessments of poster abstracts to ensure compliance with AAPS standards and scientific rigor. • Collaborated with the AAPS committee to select high-quality abstracts for presentation at the 2024 PharmSci 360 conference. • Provided constructive feedback to abstract submitters, enhancing the quality of their submissions. • Checked the relevancy of data, results, and images to ensure clarity and scientific accuracy. • Applied critical thinking and analytical skills to identify key findings and innovations in submitted abstracts. • Enhanced the quality and relevance of conference content by meticulously screening and approving abstracts.

Regulatory Affairs Intern
Vancouver, British Columbia, Canada
• Conducted comprehensive market research on pharmaceutical trends and drug repurposing, supporting strategic decisions for a Vancouver startup. • Collected and analyzed data on repurposed drugs, identified key players and societal impacts to inform marketing strategies. • Investigated regulatory barriers and intellectual property frameworks, detailed patent filings, ownership, and profit distribution in the drug repurposing market. • Compiled detailed reports featuring trends, statistics, and findings, which aided in the startup's market entry strategy. • Evaluated the potential impact of AI advancements on the drug repurposing market, providing insights into future industry shifts.
Education

Regulatory Affairs
Courses taken: Regulatory Strategy for Product Development & Life-Cycle Management Regulatory Compliance and Practice Introduction to FDA Pharmaceutical Regulation Human Experimentation Introduction to Safety Sciences Legal Issues in International Food, Drug, and Medical Device Regulation Therapeutic Product Development
Afrah Mujeeb's Contact Information
Phone
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