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Noblesville, IN 46062 .317-674-5263.janicel568@gmail.com
Janice L. Boyd
Experience
October 2015 – present ERC (Elite Research Consulting), LLC Noblesville, IN
Senior Clinical Research Associate – Independent Consultant
 Monitor clinical trials for new products, product enhancements, and product process
changes to ensure adherence to Federal regulations, company policies, and any other
applicable procedures
 15 years of medical device monitoring
October 2015 – present Hart Clinical Consultants Atlanta, GA
Senior Clinical Research Associate – Independent Consultant
 Monitoring clinical trials for multiple therapeutic areas. Working with sites from Site
Initiation Visits through Close-out Visits.
March 2014 – September 2015 Abbott Vascular (AV) Santa Clara, CA
Manager, Clinical Research
 Manage 5 direct reports on FCRA Team
 External Operations Manager of Coronary IDE Clinical Trial, providing support to project
team, coordinating site training/start-up (3000 patients, 140 sites US, Canada, Australia,
Germany)

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2008 – 2014 Abbott Vascular Santa Clara, CA
Principal Clinical Research Associate
 Monitor and/or supervise the monitoring activities of assigned clinical trials for new
products, product enhancements, and product process changes to ensure adherence to
Federal regulations, company policies, and any other applicable procedures
 Chairman of US CRA Compliance Committee – being directly involved with the inception
of the initiative in 2007 through globalization in 2012. This committee functions to
ensure that all parties engaged in clinical site monitoring activities are compliant to all
guidance documents, applicable operating procedures, Federal Regulations and Good
Clinical Practices
2006 – 2008 Abbott Vascular Santa Clara, CA
Senior Clinical Research Associate
 Site Management and monitoring of IDE coronary stent trials
2004 – 2006 Guidant Corporation (acquired by AV) Santa Clara, CA
Senior Clinical Research Associate
 Site Management and monitoring of IDE coronary stent trials
2000 – 2004 Guidant Corporation Santa Clara, CA
Clinical Research Associate II
 Site Management and monitoring of IDE coronary stent trials
1998 – 2000 Guidant Corporation Santa Clara, CA
Clinical Application Consultant
 Promote Guidant Corporation products through education of current and potential
customers and procedure coverage within a defined territory/region/area by providing

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clinical education and sales support in order to assist in achieving projected sales goals
and increasing sales revenues within assigned product lines
1995 – 1998 Northside Cardiology Indianapolis, IN
Clinical Research Coordinator
 Coordinate multiple clinical trials for a large Cardiology practice.
 Key point person to enroll and follow hundreds of clinical trial subjects
1990 – 1995 St. Vincent Hospital Indianapolis, IN
Staff Nurse
 1990 – 1992 - Staff nurse on a Medical Telemetry Unit
 1992 – 1995 – Staff nurse in the Cardiac Cath Lab
Education
RN, BSN Ball State University Muncie, IN
Licenses/Certifications
RN State of Indiana 1990
CCRP SoCRA 2001