Focused and Detail-oriented Senior Clinical Research Coordinator well-versed in study protocols, standard operating procedures, and general trial oversight. Excellent problem-solving abilities with a detail-oriented nature. Ready to bring16 years of related experience to a challenging new role. Highly organized, very thorough with good planning skills. Communicates effectively with study participants, colleagues, vendors, and study monitors.
Worked with principal investigator and sponsors to facilitate daily trial activities and comply with research protocols
Gathered, processed and shipped lab specimens
Maintained compliance with protocols covering patient care and clinical trial operations
Coordinated clinical trials focused on disorders such as Liver Disease and Gastroenterology
Collected data and followed research protocols, operations manuals and case report form requirements
Demonstrate knowledge & experience in coordination of prospective clinical research
Participated in initiation visits and investigator meetings, implementing trials in accordance with study timelines and budgets
Maintained working knowledge of Regulatory guidelines, compliance with applicable ICH-GCP guidelines, local regulatory requirements, SOP, and study specific procedures
Assist with Executing CTA
Process invoices for related cost for reimbursable items & procedures
Respond to a wide variety of inquiries from staff, PI, and outside vendors for the purpose of solving problems and providing information
Review budget request for approval
Clinical Research Coordinator III (Pediatric Gastroenterology Dept.)
Baylor College Of Medicine
Houston, Texas
04.2019 - 07.2020
Coordinated all administrative functions for planned studies, including protocol development, equipment preparation and materials purchasing
Execute clinical trials onsite and remotely
Ensure compliance with NIH and IRB regulation
Review databases and referral leads to screen for potential eligible patients
Adhered to standards in all areas, including data collection, research protocols, and regulatory reporting
Refined and contributed to special data entry projects of current & previous study trials
Maintenance of study regulatory documentation, including screening, enrollment logs & study identification logs
Assist PI in the submission of most reports, including adverse events, non-compliance, or any other unanticipated issues
Implemented a new database from scratch
Worked closely with PI and other hospital staff to maintain optimum levels of communication to effectively and efficiently complete projects
Clinical Research Coordinator III (Psychiatric Dept.)
Baylor College Of Medicine
Houston, TX
02.2008 - 10.2018
Coordinated clinical trials focused on Stimulant Addiction, which included, overseeing clinical assessment of patients participating in clinical trial studies of Cocaine, Methadone, and Nicotine
Adhered to standards in all areas, including data collection, research protocols, and regulatory reporting
Expertly conducted a full range of patient and protocol assessments, including safety and efficacy, vital signs, & administering study medications
Implemented and developed patient recruitment plans to ensure clinical trial success while training students on patient care, electronic forms & management processes to ensure the success of trials
Maintained working knowledge of Regulatory guidelines, compliance with applicable ICH-GCP guidelines, and local regulatory requirements, SOP, and study-specific procedures
Conducted in-house and sponsored clinical trial audits
Collaborated with physicians, hospital support staff, and drug companies to ensure efficient implementation of clinical trial protocols
Process and ship biological specimens according to the study protocol
Created all regulatory binders and quality control
Created spreadsheets using Microsoft Excel for daily, weekly, and monthly reporting
Education
Associate of Applied Science - Education
Lone Star College System
Spring, TX
12-2025
Skills
Research SOPs understanding
Medication dispensing
Informed consent
Good Clinical Practices
EDC (CTMS & Rave)
Specimen collection
IMedidata
Time Management
Strong Work Ethic
Suvoda
Certification
CITI Program Training (BCM) (Liver Associates of Texas)
Echosens Fibro Scan (Liver Associates of Texas)
Transporting Dangerous Goods (IATA)
Red Cap (BCM)
Good Clinical Practices (NIDA)
Protecting Human Research Participants (NIH)
Projects
NGM - A Phase2 Randomized, Double Blinded, Placebo -Controlled, study to evaluate efficacy and safety of the NGM282 (Aldafermin) in subjects with Compensated Cirrhosis, Akero - A Phase2B Randomized, Double Blinded Placebo-Controlled study evaluating the safety and efficacy of Efruxifermin in subjects with Compensated Cirrhosis, Madrigal-11- A Phase3 Double Blinded, Placebo-Controlled Controlled study to evaluate Efficacy and safety of Resmetirom in subjects with NASH, STOP-NAFLD – A Phase2 Randomized, Placebo-Controlled Clinical Trial evaluating the safety and efficacy of Losartan for treatment of Pediatric NAFLD, ACE Inhibitor - A Phase I Double Blind Placebo-Controlled Study to Evaluate the Efficacy and Safety of Perindopril as a Treatment for Methamphetamine Dependence, Rivastigmine – A Double-blind Placebo-Controlled human laboratory study demonstrating the treatment (AChE) inhibitor Rivastigmine to reduced Methamphetamine-induced craving
Senior Clinical Research Coordinator II at Rutgers Robert Wood Johnson Medical SchoolSenior Clinical Research Coordinator II at Rutgers Robert Wood Johnson Medical School