Emily Christopher Email & Phone Number

Sacramento, California, United States

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Sacramento, California, United States

• Develops and implements research protocols, including sampling design, data collection procedures, and issues of human subjects protections
• Oversees research projects, including monitoring timelines and communicating with clients/funders
• Collects and analyzes quantitative and qualitative data
• Analyzes quantitative and qualitative data
• Prepares reports and presents research findings to various stakeholders.

Sacramento, California, United States

• Designed a curriculum for population health-focused multisector collaboratives
• Design and implement research activities
• Conduct literature reviews
• Perform qualitative and quantitative analysis
• Coordinate and manage activities and timelines for projects
• Regularly engage numerous external partners, to present work and collaborate on specific activities

Sacramento, California Area

• Provide technical support on projects to advance the multipurpose prevention technology (MPT) field, including but not limited to creating a mapping tool to identify target populations for MPTs and developing a.
• Support projects focused on communications and outreach around MPTs and maintaining the MPT Product Development Database
• Present MPT-related work at conferences representing the Initiative for MPTs (IMPT) and engage in other partner networks and professional associations
• Work closely with a small team at CAMI Health, as well as external colleagues and consultants across the globe

Cape Town Area, South Africa

• Responsible for study start-up and materials development for MTN-025
• Recruited and managed study start-up and clinic visits for 14 participants inthe Informed Consent Pilot Study
• Coordinated MTN-015 and MTN-016, following over 20 study participants
• Trained and supervised research team to ensure effective and efficientimplementation of study procedures across four studies
• Managed ongoing trial compliance with American and South Africanregulatory bodies
• Designed, developed, documented, and maintained policies and proceduresfor research participant registration and protocol implementation

Seattle, WA

• Independently managed four Huntington Disease clinical trials, ensuring compliance with university, local, and federal regulations
• Coordinated study visits and procedures with patients, physicians, sponsors, and other personnel, and administered cognitive tests
• Designed, developed, documented, and maintained policies and procedures for patient registration and protocol implementation
• Recruited over 50 study participants for ENROLL-HD, FIRST-HD and ARC- HD
• Followed an additional 20+ participants in PREDICT-HD

Greater Seattle Area

• Supported Research Nurse and Coordinators in the conduct of both NIH and industry sponsored drug and device clinical trials
• Coordinated the DAPT study, involving study patient management, screening, scheduling, and managing medical records
• Created and submitted study and regulatory documents

Greater Seattle Area

• Worked closely with Staff Scientist, Principal Investigator and sites in New Mexico and Wisconsin in the conduct of a cross-sectional epidemiological trial, Metals Exposure in Residents of Southern New Mexico
• Managed regulatory compliance, study database, and biospecimen tracking
• Created study documents and literature for study participants and staff
• Contributed to several papers on the project

Greater Seattle Area

• Performed administrative duties for the Colon Cancer Family Registry (C- CFR) including taking minutes, arranging meetings, and tracking regulatory approval for sites within the consortium
• Coordinated the annual C-CFR Steering Committee meeting, with attendees from international and domestic sites
• Created and managed SurveyMonkey polls and other methods to facilitate coordination between consortium sites
• Edited and compiled NIH-funded grant applications

Greater Seattle Area

• Screened and scheduled patients for women’s health-related studies, determined study eligibility, and explained study procedures to patients
• Created study documents, managed participant tracking databases, and designed new record-keeping systems for study participant contacts
• Worked with site Principal Investigator, Doctors, and Research Coordinators to schedule and maintain contact with study participants
• Expanded recruitment methods for women’s health-focused clinical research studies, recruiting up to 250 participants

Managed event planning for national research studies. Found and recruited consumers to participate in market research studies. Coordinated theirschedules with those of researchers. Managed and communicated schedules and logistics for the research team. Created recruiting department training manual. Implemented many consumer outreach methods such as an.

Master Of Public Health (M.P.H.), Health Services/ Maternal And Child Health

Bachelor Of Arts (B.A.), Public Health