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Noblesville, IN 46062 .317-674-5263.[email protected] 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 Page 1 of 4

Janice Boyd CV

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Noblesville, IN 46062 [email protected]

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

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