Denise Hines, BS, RN, BSN, Sr. CRA

Sr. Clinical Research Associate at Veristat
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Contact Information
us****@****om
(386) 825-5501
Location
Detroit Metropolitan Area
Languages
  • English Full professional proficiency
Skills

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5.0

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Alan Susser

Denise joined a tight-knit group and fit right in. She was a terrific clinical research associate, adding great value to our clinical research studies. She has a strong clinical knowledge and was a pleasure to work with. I highly recommend Denise to any origanization.

Karen Greenwell

Denise is an excellent monitor, and a dependable, reliable team player. Going the extra mile is routine for Denise.

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Credentials

  • Betty Liu on Career Success
    LinkedIn
    Sep, 2018
    - Nov, 2024

Experience

  • Veristat
    • United States
    • Research Services
    • 300 - 400 Employee
    • Sr. Clinical Research Associate
      • Oct 2022 - Present

      Evaluated study sites, initiated new study sites, monitored study sites, closed out study sites, and ensured that the clinical research studies are conducted under protocol guidelines set forth by the FDA, GCP’s, Sponsor and CRO. Evaluated study sites, initiated new study sites, monitored study sites, closed out study sites, and ensured that the clinical research studies are conducted under protocol guidelines set forth by the FDA, GCP’s, Sponsor and CRO.

  • Innovaderm Research Inc.
    • Canada
    • Pharmaceutical Manufacturing
    • 200 - 300 Employee
    • Sr. Clinical Research Associate
      • Dec 2021 - Present

      Evaluated study sites, initiated new study sites, monitored study sites, closed out study sites, and ensured that the clinical research studies are conducted under protocol guidelines set forth by the FDA, GCP’s, Sponsor and CRO. Evaluated study sites, initiated new study sites, monitored study sites, closed out study sites, and ensured that the clinical research studies are conducted under protocol guidelines set forth by the FDA, GCP’s, Sponsor and CRO.

  • Premier Research
    • United States
    • Biotechnology Research
    • 700 & Above Employee
    • Sr. Clinical Research Associate
      • Aug 2021 - Dec 2021

      Evaluated study sites, initiated new study sites, monitored study sites, closed out study sites, and ensured that the clinical research studies are conducted under protocol guidelines set forth by the FDA, GCP’s, Sponsor and CRO. Evaluated study sites, initiated new study sites, monitored study sites, closed out study sites, and ensured that the clinical research studies are conducted under protocol guidelines set forth by the FDA, GCP’s, Sponsor and CRO.

  • PRA Health Sciences
    • United States
    • Research Services
    • 700 & Above Employee
    • Sr. Clinical Research Associate
      • Dec 2019 - Aug 2021

      Evaluated study sites, initiated new study sites, monitored study sites, closed out study sites, and ensured that the clinical research studies are conducted under protocol guidelines set forth by the FDA, GCP’s, Sponsor and CRO. Evaluated study sites, initiated new study sites, monitored study sites, closed out study sites, and ensured that the clinical research studies are conducted under protocol guidelines set forth by the FDA, GCP’s, Sponsor and CRO.

  • Green Key Resources placed with Medtronic, Northridge, CA.
    • Flint, MI
    • Sr. Regional Clinical Research Associate - Contract
      • Nov 2017 - Jul 2018

      Evaluated study sites, initiated new study sites, monitored study sites, closed out study sites, and ensured that the clinical research studies are conducted under protocol guidelines set forth by the FDA, GCP’s, Sponsor and CRO. Evaluated study sites, initiated new study sites, monitored study sites, closed out study sites, and ensured that the clinical research studies are conducted under protocol guidelines set forth by the FDA, GCP’s, Sponsor and CRO.

  • inVentiv Health Clinical placed with Leo Pharma - Madison, NJ
    • Princeton, NJ
    • Sr. Regional Clinical Research Associate - Contract
      • Feb 2017 - Jun 2017

      Evaluated study sites, initiated new study sites, monitored study sites, closed out study sites, and ensured that the clinical research studies are conducted under protocol guidelines set forth by the FDA, GCP’s, Sponsor and CRO. Evaluated study sites, initiated new study sites, monitored study sites, closed out study sites, and ensured that the clinical research studies are conducted under protocol guidelines set forth by the FDA, GCP’s, Sponsor and CRO.

  • Real Staffing placed with Medtronic - Northridge, CA.
    • Chicago, IL
    • Sr. Regional Clinical Research Associate - Contract
      • Oct 2015 - Aug 2016

      Evaluated study sites, initiated new study sites, monitored study sites, closed out study sites, and ensured that the clinical research studies are conducted under protocol guidelines set forth by the FDA, GCP’s, Sponsor and CRO. Evaluated study sites, initiated new study sites, monitored study sites, closed out study sites, and ensured that the clinical research studies are conducted under protocol guidelines set forth by the FDA, GCP’s, Sponsor and CRO.

  • INC Research
    • United States
    • Pharmaceutical Manufacturing
    • 700 & Above Employee
    • Sr. Regional Clinical Research Associate - Contract
      • Apr 2015 - Jun 2015

      Evaluated study sites, initiated new study sites, monitored study sites, closed out study sites, and ensured that the clinical research studies are conducted under protocol guidelines set forth by the FDA, GCP’s, Sponsor and CRO. Evaluated study sites, initiated new study sites, monitored study sites, closed out study sites, and ensured that the clinical research studies are conducted under protocol guidelines set forth by the FDA, GCP’s, Sponsor and CRO.

  • Premier Research
    • United States
    • Biotechnology Research
    • 700 & Above Employee
    • Sr. Regional Clinical Research Associate - Contract
      • Aug 2014 - Dec 2014

      Evaluated study sites, initiated new study sites, monitored study sites, closed out study sites, and ensured that the clinical research studies are conducted under protocol guidelines set forth by the FDA, GCP’s, Sponsor and CRO. Evaluated study sites, initiated new study sites, monitored study sites, closed out study sites, and ensured that the clinical research studies are conducted under protocol guidelines set forth by the FDA, GCP’s, Sponsor and CRO.

  • The Artac Seel Company
    • United States
    • Pharmaceutical Manufacturing
    • Sr. Regional Clinical Research Associate - Contract
      • Nov 2012 - Oct 2013

      Evaluated study sites, initiated new study sites, monitored study sites, closed out study sites, and ensured that the clinical research studies are conducted under protocol guidelines set forth by the FDA, GCP’s, Sponsor and CRO. Placed at TKL Research - Rochelle Park, NJ. Evaluated study sites, initiated new study sites, monitored study sites, closed out study sites, and ensured that the clinical research studies are conducted under protocol guidelines set forth by the FDA, GCP’s, Sponsor and CRO. Placed at TKL Research - Rochelle Park, NJ.

  • Clinical Resource Network (CRN)
    • United States
    • Staffing and Recruiting
    • 1 - 100 Employee
    • Sr. Regional Clinical Research Associate - Contract
      • Feb 2010 - Nov 2012

      Evaluated study sites, initiated new study sites, monitored study sites, closed out study sites, and ensured that the clinical research studies are conducted under protocol guidelines set forth by the FDA, GCP’s, Sponsor and CRO. Placed at INC Research - Austin, TX. Evaluated study sites, initiated new study sites, monitored study sites, closed out study sites, and ensured that the clinical research studies are conducted under protocol guidelines set forth by the FDA, GCP’s, Sponsor and CRO. Placed at INC Research - Austin, TX.

  • University of Michigan
    • United States
    • Higher Education
    • 700 & Above Employee
    • Clinical Monitor
      • Nov 2008 - May 2009

      Monitored NIH study sites and ensured that the clinical research studies are conducted under protocol guidelines set forth by the FDA, GCP’s, Sponsor and CRO. Monitored NIH study sites and ensured that the clinical research studies are conducted under protocol guidelines set forth by the FDA, GCP’s, Sponsor and CRO.

  • inVentiv Health Clinical
    • United States
    • Pharmaceutical Manufacturing
    • 500 - 600 Employee
    • Sr. Regional Clinical Research Associate
      • Mar 2007 - Aug 2008

      Evaluated study sites, initiated new study sites, monitored study sites, closed out study sites, and ensured that the clinical research studies are conducted under protocol guidelines set forth by the FDA, GCP’s, Sponsor and CRO. Evaluated study sites, initiated new study sites, monitored study sites, closed out study sites, and ensured that the clinical research studies are conducted under protocol guidelines set forth by the FDA, GCP’s, Sponsor and CRO.

  • Kendle International Inc
    • United States
    • Research Services
    • 1 - 100 Employee
    • Sr. Regional Clinical Research Associate
      • Jan 2006 - May 2006

      Evaluated study sites, initiated study sites, monitored study sites, closed out study sites, and ensured that the clinical research studies are conducted under protocol guidelines set forth by the FDA, GCP’s, Sponsor and CRO. Evaluated study sites, initiated study sites, monitored study sites, closed out study sites, and ensured that the clinical research studies are conducted under protocol guidelines set forth by the FDA, GCP’s, Sponsor and CRO.

  • i3 Research
    • Pharmaceutical Manufacturing
    • 200 - 300 Employee
    • Sr. Regional Clinical Research Associate
      • Jul 2003 - Jun 2005

      Evaluated study sites, initiated study sites, monitored study sites, closed out study sites, and ensured that the clinical research studies are conducted under protocol guidelines set forth by the FDA, GCP’s, Sponsor and CRO. . Evaluated study sites, initiated study sites, monitored study sites, closed out study sites, and ensured that the clinical research studies are conducted under protocol guidelines set forth by the FDA, GCP’s, Sponsor and CRO. .

  • ACRP
    • CCRA Certification
      • Nov 2001 - Nov 2003

  • PPD
    • United States
    • Research Services
    • 700 & Above Employee
    • Sr. Regional Clinical Research Associate
      • Apr 2002 - Jul 2003

      Evaluated study sites, initiated study sites, monitored study sites, closed out study sites, and ensured that the clinical research studies are conducted under protocol guidelines set forth by the FDA, GCP’s, Sponsor and CRO. Evaluated study sites, initiated study sites, monitored study sites, closed out study sites, and ensured that the clinical research studies are conducted under protocol guidelines set forth by the FDA, GCP’s, Sponsor and CRO.

  • Sanofi
    • France
    • Pharmaceutical Manufacturing
    • 700 & Above Employee
    • Regional Clinical Research Associate
      • Oct 2000 - Apr 2002

      Evaluated study sites, initiated study sites, monitored study sites, closed out study sites, and ensured that the clinical research studies are conducted under protocol guidelines set forth by the FDA, GCP’s, Sponsor and CRO. Evaluated study sites, initiated study sites, monitored study sites, closed out study sites, and ensured that the clinical research studies are conducted under protocol guidelines set forth by the FDA, GCP’s, Sponsor and CRO.

  • SCIREX Corporation
    • Pharmaceutical Manufacturing
    • 1 - 100 Employee
    • Regional Clinical Research Associate
      • Jun 1999 - Jul 2000

      Evaluated new studies, initiated new study sites, monitored study sites, closed out study sites, and ensured that the clinical research studies are conducted under protocol guidelines set forth by the FDA, GCP’s, Sponsor and CRO. Evaluated new studies, initiated new study sites, monitored study sites, closed out study sites, and ensured that the clinical research studies are conducted under protocol guidelines set forth by the FDA, GCP’s, Sponsor and CRO.

  • Statprobe Inc
    • United States
    • Pharmaceutical Manufacturing
    • Clinical Research Associate
      • Sep 1997 - Jun 1999

      Evaluated study sites, initiated study sites, monitored study sites, closed out study sites, and ensured that the clinical research studies are conducted under protocol guidelines set forth by the FDA, GCP’s, Sponsor and CRO. Evaluated study sites, initiated study sites, monitored study sites, closed out study sites, and ensured that the clinical research studies are conducted under protocol guidelines set forth by the FDA, GCP’s, Sponsor and CRO.

  • Genesys Regional Medical Center - Medical Procedures Unit
    • Grand Blanc, MI
    • Registered Nurse
      • Feb 1997 - Sep 1997

      Performed assessments, coordinated care plans, evaluated effectiveness of care, performed patient education, recovered/discharged patients with coronary, respiratory, gastrointestinal, and chronic pain. Cross-trained in phlebotomy, bronchoscopy, endoscopy, and an infinite variety of other medical procedures. Performed assessments, coordinated care plans, evaluated effectiveness of care, performed patient education, recovered/discharged patients with coronary, respiratory, gastrointestinal, and chronic pain. Cross-trained in phlebotomy, bronchoscopy, endoscopy, and an infinite variety of other medical procedures.

  • Genesee Memorial Hospital - Pain Management Cener
    • Flint, MI
    • Registered Nurse
      • Jul 1996 - Feb 1997

      Performed assessments, coordinated care plans, evaluated effectiveness of care, performed patient education, recovered/discharged patients with chronic pain. Performed assessments, coordinated care plans, evaluated effectiveness of care, performed patient education, recovered/discharged patients with chronic pain.

  • St. Joseph Hospital - Coronary Care Unit and Progressive Coronary Care Unit
    • Flint, MI
    • Registered Nurse
      • May 1994 - Jul 1996

      Performed assessments, coordinated care plans, evaluated effectiveness of care, performed patient education and discharged patients with coronary and respiratory disease. Performed assessments, coordinated care plans, evaluated effectiveness of care, performed patient education and discharged patients with coronary and respiratory disease.

Education

  • University of Michigan
    Nursing, RN, BSN
    1990 - 1994
  • University of Michigan-Flint
    BS, Biology
    1985 - 1990

Community

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