•Collected data and followed research protocols, operations manuals and case report form requirements.•Screened patient records, databases and physician referrals to identify prospective candidates for research studies.•Participated in initiation visits and investigator meetings, implementing trials in accordance with study timelines and budgets.•Worked with principal investigator and sponsors to facilitate daily trial activities and comply with research protocols.•Created plans and communicated deadlines to ensure projects were completed on time.•Resolved problems, improved operations and provided exceptional service.•Worked closely with Site Manager to maintain optimum levels of communication to effectively and efficiently complete projects.•Followed informed consent processes and maintained records.•Gathered, processed and shipped lab specimens.•Maintained compliance with protocols covering patient care and clinical trial operations.

• Interpreted and analyzed research data to draw conclusions on outcomes.• Achieved project goals accurately and with sense of urgency.• Performed routine data analysis to correct and verify data entry.• Prepared materials for reports, presentations and submission to peer-reviewed journal publications.• Prepared fact sheets, tables and graphs to summarize research results.

Health Promotion Internship•Nutrition and exercise program planning•Smoking cessation classes