Rebecca Ebert Email & Phone Number

• Expertise with eCOA implementation including licensing, configuration, and translations through engagement with customers and vendors, including extensive experience working with CROs and sponsors alike to reach.
• Assures processes are maintained, project reporting remains current, change management is documented, timelines are adhered to, and projects are completed within scope, while also proactively maintaining both sponsor.
• Responsible for all activities related to the implementation of decentralized clinical trials including strategic planning, managing workflows, executing project management plans and timelines, coordinating with.

• Leverages thorough knowledge of the clinical trial process, regulatory requirements (i.e. GCP), and Software as a Service (SaaS), along with critical-thinking skills and a detail-oriented mindset to ensure projects are.
• Collaborates with cross-functional teams, including product management, data management, and compliance, fostering effective communication and synergy

Los Angeles, California

• Contributor on a proposal that was awarded a DOD grant to examine Special Operations Warfighter Performance through novel biomarker identification and biometric monitoring using mobile apps, wearable sensors, and devices
• Co-authored a peer-reviewed manuscript on Reconnaissance Marine Training, the results of which were covered by The Economist
• Co-managed conference proceedings on technology-based solutions to address healthcare disparities with over 1000 attendees
• Developed project budgets, allocated resources efficiently, and optimized financial resources throughout the clinical trial process
• Managed the internship program that offers mentoring and clinical trial exposure to a diversity of students

• Managed a study focused on the health impacts of social isolation, resulting in a journal publication and conference presentation
• Managed all research aspects including grant writing and proposal development, protocol design, IRB submission and approval process, participant recruitment and consent procedures, data management, and publication of.

Pittsburgh, Pennsylvania

• As a crucial member of the Pediatric Infectious Disease research team, I coordinated several studies simultaneously, working directly with medical personnel, investigators, and patients, examining vaccine efficacy with.
• Coordinated myriad studies, which included protocol analysis, participant recruitment and enrollment, informed consent, data collection and entry, research meeting presentations, and sponsor updates
• Supervised and trained student workers in this role.

White Oak, PA

As a licensed EMT, I responded to 911 calls in the community and performed pre-hospital patient care to sick and injured persons, while collaborating and communicating with healthcare workers, team members, hospitals, and first responders, to facilitate seamless operating procedures and to ensure ideal patient outcomes

Pittsburgh, PA

As an Undergraduate Student Research Associate, I designed and published two peer-reviewed research papers: 1) a review of sedative medication use and 2) analysis of maternal sleep behavior in early gestation pregnancy and correlations with adverse outcomes, as first author

Los Angeles, CA

Assisted in advancing the ground-breaking, longitudinal Women’s Ischemia Syndrome Evaluation Study, investigating ideal diagnostic and treatment protocols for women’s heart disease, through data management and patient engagement

Bachelor Of Science - Bs, Psychology

With focus in Chemistry and Biological Sciences

Education record