Syed Rizvi
San Antonio,TX
Summary
Experienced in Clinical Research with focus on study planning, data collection, and trial management. Familiar with regulatory guidelines and clinical procedure oversight. Strong communication skills coupled with ability to manage multi-faceted projects effectively contribute to comprehensive execution of clinical research studies. Previous work has demonstrated significant improvements in efficiency and accuracy of data collection processes. Proficient in clinical trial management software (e.g Medidata, Veeva Vault, TI.
Overview
7
7
years of professional experience
Work History
Clinical Research Associate
Riz research LLC
San Antonio, TX
10.2021 - Current
- Performed clinical research activities including protocol development, subject recruitment and data collection.
- Reviewed and monitored clinical trial sites to ensure compliance with Good Clinical Practices guidelines.
- Coordinated the submission of regulatory documents to IRBs and ECs and other relevant authorities.
- Provided support in writing informed consent forms, patient diaries, study manuals.
- Ensured proper storage of investigational product at investigator sites per GCP guidelines.
- Interacted with sponsors, CROs, investigators, vendors and subcontractors as needed.
- Monitored safety events reported during the course of clinical trials in accordance with SOPs.
- Maintained strict confidentiality to keep personal information and collected data private.
- Performed pre-study, closeout and interim visits to check on study activities.
- Evaluated proof of eligibility and consent for participants.
- Recruited and selected potential research subjects.
- Spearheaded qualification, initiation, monitoring and close out visits by coordinating with project management team.
- Monitored site activities and sent follow-up letters to participants.
- Conducted site initiation visits and monitored ongoing studies at investigator sites.
Pharmacy Assistant
D Watson
Islamabad, Punjab
01.2018 - 05.2021
- Answered customer inquiries regarding drug interactions, side effects and dosage instructions.
- Provided guidance on the selection of over-the-counter medications and supplements.
- Received telephone calls from physicians, nurses or other healthcare professionals requesting information about medications or supplies.
- Answered customer questions about prescribed and OTC medications.
- Trained new pharmacy staff in procedures and customer service standards.
- Assisted pharmacist in daily operations tasks and administrative tasks.
Education
Attended Pharmacy School For 4 Years - Pharm D
University of Sargodha
Pakistan 12-2019
Skills
- Protocols development
- Good clinical practice
- Completing regulatory documents
- Clinical Documentation
- Data Collection
- Status Reporting
- Patient Safety
- Patient recruitment
- Site Management
- Research and Development
- Site monitoring
- Monitoring visits
- Detailed documentation
- Report Writing
- Patient recruitment strategies
- Trip reports
Languages
English
Full Professional
Urdu
Native/ Bilingual
Affiliations
- Gardening
- Cricket
- Football
References
References available upon request.
Timeline
Clinical Research Associate
Riz research LLC
10.2021 - Current
Pharmacy Assistant
D Watson
01.2018 - 05.2021
Attended Pharmacy School For 4 Years - Pharm D
University of Sargodha
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