Jacqueline De La Rosa

• Replenishing and stocking inventory
• Blinded assessor for certain protocols
• Data entry and electronic data capture systems

Medrio, Ecaselinks, Veeva Vault, Viedoc, Yprime, Imedidata

• Marketing/Recruiting Subjects- TV ADS
• Reduced data entry errors by implementing stringent quality control measures throughout the study lifecycle.
• Followed clinical research protocols and conducted study visits in compliance with ICH/GCP and FDA regulations.
• Monitored adverse events and ensured timely reporting to regulatory bodies, maintaining high safety standards.
• Screened patient records, databases, and physician referrals to identify prospective candidates for research studies.
• Streamlined patient visit schedules, reducing wait times and increasing patient satisfaction.
• Followed informed consent processes and maintained records.
• Collaborated with clinical staff and other healthcare professionals to support clinical trial data accuracy.
• Coordinated and monitored clinical trial activities to support timely and accurate completion of studies.
• Worked with principal investigator and sponsors to facilitate daily trial activities and comply with research protocols.
• Facilitated clear communication between principal investigators, sponsors, and study participants for seamless trial execution.
• Assessed patients'' eligibility criteria following strict adherence to inclusion/exclusion guidelines.
• Trained new team members on essential clinical research protocols and procedures, promoting a culture of continuous learning.

• Packaging medication in different doses and meeting deadlines
• Ordering and stocking medication inventory
• Billing medication to insurance
• Answering phone calls
• Accounting

• Assisting customers in front end of store by checking out items and bagging in timely manner
• Replenishing and stocking inventory
• Answering phones