Rebecca Stilley Email & Phone Number

Lenexa, Kansas, United States

Lenexa, Kansas, United States

• Liaise with principal investigators and staff to facilitate daily trial activities, verify compliance with research protocols and sponsor requirements, and communicate with research study participants.
• Lead project kick-off and review meetings to help establish study frameworks and deliverables schedules.
• Conduct and lead site initiation and monitoring visits in partnership with the data entry team.
• Document and collate study instructions, and source and clinic documentation.
• Oversee the collection and transmission of research data samples, adhering to robust study integrity standards.
• Verify the completion and accuracy of relevant consent forms, study volunteer data, and case reports while monitoring study budgets and addressing variance to targets.

Lenexa, Kansas, United States

• Liaise with principal investigators and staff to facilitate daily trial activities, verify compliance with research protocols and sponsor requirements, and communicate with research study participants.
• Lead project kick-off and review meetings to help establish study frameworks and deliverables schedules.
• Conduct and lead site initiation and monitoring visits in partnership with the data entry team.
• Document and collate study instructions, and source and clinic documentation.
• Oversee the collection and transmission of research data samples, adhering to robust study integrity standards.
• Verify the completion and accuracy of relevant consent forms, study volunteer data, and case reports while monitoring study budgets and addressing variance to targets.

Lenexa, Kansas, United States

• Assessed clinical trial data’s compliance with industry standards, regulations, and internal processes
• Oversaw and managed clinical trial data entry processes while addressing data quality inquiries, and deviations from internal and external reviewers.
• Innovated methods for data entry and QC of study documentation and verified accurate source data collection.

Overland Park, Kansas, United States

• Established the benchmarks of clinical research data collection excellence, meeting all study requirements and KPIs.
• Verified data collected and processed according to eCRF guidelines and established GDPs and SOPs.
• Participated in sponsor review sessions to assess data management processes.
• Identified and logged data discrepancies and errors.
• Contributed to ongoing quality assurance efforts through auditing data management and entry activities.

Overland Park, Kansas, United States

• Met defined study and project timelines to complete key data entry tasks.
• Monitored the diligent completion of required data fields.
• Collected data from a range of source documentation and data capture systems.
• Liaised with the relevant Data Management teams to obtain required data reports.

Overland Park, Kansas, United States

• Collected and analyzed physical and digital biological data and samples.
• Provided extensive administrative and operational support, including attending to patient needs, taking vitals, blood running, VAS testing, serving meals, and conducting Pupillometry examinations.

Bachelor'S Degree, Health/Health Care Administration/Management

Associate Of Arts And Sciences - Aas, General Studies

Activities and Societies: Phi Theta Kappa