Lara Coffin
Project Director @Ucsf Division Of Prevention Science
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WORK HISTORY
Project Director @Ucsf Division Of Prevention Science
San Francisco, CA, US
Oversee the administrative, operational, and financial aspects of a multi-site study evaluating a smartphone-based Contingency Management and positive affect intervention to enhance PrEP adherence among stimulant users.• Hire, train and supervise field staff and complete performance evaluations; Ensure that staff are trained on existing and new protocols. Cultivate communication and teamwork between collaborating study sites.• Develop and maintain study protocols and standard operating procedures, ensuring data integrity and compliance with collection protocols.• Monitor participant recruitment and retention, collaborating with the data manager to develop databases and tracking systems. Perform regular quality assurance.• Regulatory Oversight: Review all protocols and develop IRB documentation for submission, track and update all IRB submission renewals and modifications as needed. Prepare reports for the Data and Safety Monitoring Board.• Fiscal Management: work with PIs in budget preparation, progress reports, and carry forward requests. Work with the financial analyst to monitor fiscal expenditures and budget status reports.• Coordinate and facilitate meetings with investigators, staff, and community-based organizations to promote collaboration and study goals.
EDUCATION
University of California, Santa Cruz
Bachelor of Science - BS, Biology, General
University of Michigan
MPH, Health Behavior/Health Education
SKILLS
ABOUT LARA COFFIN
As a Project Director at the University of California, San Francisco (UCSF), I oversee the administrative, operational, and financial aspects of multi-site studies evaluating innovative interventions to enhance medication adherence among people who use substances. With over 10 years of experience in clinical research, I have developed and maintained study protocols and standard operating procedures, ensuring data integrity and compliance with collection protocols. I also hire, train, and supervise field staff, fostering communication and teamwork between collaborating study sites, providers and community resources. Additionally, I am a Certified Clinical Research Professional (CCRP) issued by SOCRA, demonstrating my commitment to ethical and high-quality research practices. My goal is to contribute to the advancement of disease prevention and treatment through evidence-based interventions.
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