NOUR LUTFI
ON
Summary
Knowledgeable Clinical Research Coordinator adept at recognizing clinical values and abstracting data from source documents. Skilled in using analytical abilities to identify data and patient safety issues. I have managed 10+ research studies from site initiation to closeout. I excel in handling patient information, laboratory samples, and compliance procedures, overseeing medication administration, patient monitoring, and specimen collection with strict adherence to clinical trial protocols and regulatory requirements.
With excellent communication, planning, and problem-solving skills, I efficiently manage trial schedules, results, and adverse events. Holding a postgraduate certificate in clinical research, drug safety, and pharmacovigilance, I am well-versed in study protocols, SOPs, and federal regulations, aiming to excel as a Clinical Research Coordinator.
Overview
3
3
years of professional experience
1
1
Certification
Work History
Clinical Research Coordinator
Derma Clinic ( Guelph Dermatology Research)
06.2022 - 06.2024
- Assessed patients'' eligibility criteria following strict adherence to inclusion/exclusion guidelines.
- Screened patient records, databases, and physician referrals to identify prospective candidates for research studies.
- Reviewed referral information and kept track of intakes from various referral sources.
- Streamlined data collection processes for increased efficiency and accuracy in study results.
- Directed site initiation visits, establishing key partnerships with local healthcare providers to facilitate successful trial implementation.
- Trained new team members on essential clinical research protocols and procedures, promoting a culture of continuous learning.
- Oversaw the management of investigational product supplies, ensuring appropriate storage conditions were maintained at all times for optimal efficacy during trials.
- Reduced data entry errors by implementing stringent quality control measures throughout the study lifecycle.
- Followed informed consent processes and maintained records.
- Participated in initiation visits and investigator meetings, implementing trials following study timelines and budgets.
- collected, processed, and shipped lab specimens.
- Enhanced patient safety by meticulously monitoring and documenting adverse events during clinical trials.
- Worked with principal investigator and sponsors to facilitate daily trial activities and comply with research protocols.
- Screened patient records, databases, and physician referrals to identify prospective candidates for research studies.
- Reviewed referral information and kept track of intakes from various referral sources.
Clinical Research Coordinator
Nutrasource
11.2021 - 06.2022
- Screened patient records and databases to identify prospective candidates for research studies
- Collected data and followed research protocols, operations manuals and case report form
- Followed informed consent processes and maintained records
- Collected, evaluated and modeled collected data
- Worked with principal investigator and sponsors to facilitate daily trial activities and comply with research protocols
- Oversaw adverse events case reporting and conducted follow-up with participants.
- Used coordination and planning skills to achieve results according to schedule
- Offered friendly and efficient service to customers, handled challenging situations with ease.
Education
Post Graduate Diploma - Clinical Research ,Pharmacovigilance ,Drug Safety
Academy of Applied Pharmaceutical Science
Mississauga, Ontario, Canada11.2021
Bachelor Degree - Pharmacy And Pharmaceutical Chemistry
Kalamoon University
Damascus, Syria09.2009
Skills
- Patient recruitment, screening, and enrolment
- Perform vitals, ECG
- Database maintenance and Schedule Coordination
- Interpersonal and Communication Skills
- MS Excel
- Adverse event collecting and reporting
- Specimen handling and shipping
- Phlebotomy
- Site Management
- Electronic Data Capture
- Investigational product management
- Informed Consent Process
- Task Prioritization
Certification
- Introduction to Pharmacovigilance and signal Detection - Uppsala Monitoring Center - March/2021
- (TCP: CORE ) Tri- council policy statement: Ethical Conduct for Research Involving Humans Course on Research Ethics - Panel on Research Ethics - Oct /2021
- Good Clinical Practice - Issued Jan/ 2024
- Health Canada Division 5 - Issued Jan/2024
- CITI Canada Privacy Course CITI Program - Issued December/2021
- Responsible conduct of Research - Life science CITI Program - Issued December/2021
- Transportation of Dangerous Goods TDG/IATA ,Mayo clinic - Issued Jun/2024
Websites
Timeline
Clinical Research Coordinator
Derma Clinic ( Guelph Dermatology Research)
06.2022 - 06.2024
Clinical Research Coordinator
Nutrasource
11.2021 - 06.2022
Post Graduate Diploma - Clinical Research ,Pharmacovigilance ,Drug Safety
Academy of Applied Pharmaceutical Science
Bachelor Degree - Pharmacy And Pharmaceutical Chemistry
Kalamoon University
- Introduction to Pharmacovigilance and signal Detection - Uppsala Monitoring Center - March/2021
- (TCP: CORE ) Tri- council policy statement: Ethical Conduct for Research Involving Humans Course on Research Ethics - Panel on Research Ethics - Oct /2021
- Good Clinical Practice - Issued Jan/ 2024
- Health Canada Division 5 - Issued Jan/2024
- CITI Canada Privacy Course CITI Program - Issued December/2021
- Responsible conduct of Research - Life science CITI Program - Issued December/2021
- Transportation of Dangerous Goods TDG/IATA ,Mayo clinic - Issued Jun/2024
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