Nour Lutfi Email & Phone Number

Guelph, Ontario, Canada

Study Planning & Execution:Led multiple clinical studies, managing timelines, budgets, and resources efficiently.Prepared and participated in study initiation visits and investigator meetings.Managed over 10 projects simultaneously, maintaining attention to detail and meeting strict deadlines.Patient Management:Assessed patient eligibility following strict inclusion/exclusion criteria.Monitored patient safety, meticulously documenting adverse events and ensuring… Show more Study Planning & Execution:Led multiple clinical studies, managing timelines, budgets, and resources efficiently.Prepared and participated in study initiation visits and investigator meetings.Managed over 10 projects simultaneously, maintaining attention to detail and meeting strict deadlines.Patient Management:Assessed patient eligibility following strict inclusion/exclusion criteria.Monitored patient safety, meticulously documenting adverse events and ensuring adherence to protocols.Screened patient records and referrals to identify suitable research candidates.Data & Compliance Oversight:Streamlined data collection processes for improved accuracy and efficiency.Maintained accurate case report forms (CRFs) and source documents for traceability.Conducted informed consent processes, ensuring thorough documentation and compliance.Stakeholder Communication:Liaised with investigators to identify, assess, and resolve performance and compliance issues.Facilitated issue resolution through effective communication with sponsors, monitors, and stakeholders.Answered site feasibility assessments for potential trials.Team Leadership & Training:Trained new team members on clinical research protocols, fostering a culture of continuous learning.Promoted Good Documentation Practices (GDP) and reduced quality control errors through mentorship.Operational Management:Managed investigational product supplies, ensuring proper storage and handling.Collected, processed, and shipped lab specimens in accordance with protocol requirements.Ensured drug storage procedures complied with SOPs and regulatory standards. Show less

Guelph, Ontario, Canada

Guelph, Ontario, Canada

Guelph, Ontario, Canada

Damascus, Syria

Postgraduate Diploma, Clinical Research, Pharmacovigilance And Drug Safety

Activities and Societies: Write study protocols, ICF, SOP. Monitor and manage clinical trials, conduct drug safety, and pharmacovigilance.

Bachelor Of Pharmacy - Bpharm

Bachelor'S Degree, Pharmacy, Pharmaceutical Sciences, And Administration