Senior Clinical Research Nurse

SHERRIE L. KINCAID, RN

CRA Services, LLC

431 Everest Dr.

Cedar Hill, Texas 75104

(Dallas-Ft. Worth metroplex)

Cell: [phone] Fax: [phone]

Email: [e-mail]

EDUCATION:

October, 2012 – present Liberty University

Lynchburg, VA

Pursuing Master of Divinity degree

with a Chaplaincy concentration

May, 1990 Texas Woman’s University

Denton, Texas

Master of Arts - Health Education

May, 1983 Texas Woman’s University

Denton, Texas

Bachelor of Science - Nursing

December, 1981 Mountain View College

Dallas, Texas

Associates of Arts and Sciences

September, 2006 International TEFL Teacher Training

English as a Foreign Language

Certificate awarded: # ITTT00162717

April, 2007 The International TEFL Corporation

Teaching of Business English

Certificate awarded: # TITCBE638

HIGHLIGHTS:

· 15 years of industry and CRA experience

· 1.5 years as a Kforce/Amgen Site Manager

o 3 years oncology experience

o Phases I - III

· 1.5 years of Leukemia monitoring experience while

o Phases I - III

· 4 years device experience

o cardiac, vascular and renal

· Medidata Rave 5.6.4 Certified Monitor

· EDC experienced in InForm, eTrials, Data Trak, IMPACT, Rave Medi Data and Oracle Clinical

· Adult Critical Care Nurse

o From 1993 – 1998 worked as a Senior Research Coordinator at UT Southwestern Medical Center at Dallas Infectious Disease Dept. working with HIV clinical trials

o From 1997 – 2002 worked full and part time in the surgical and medical ICU at St. Paul Medical Center and Zale Lipshy University Medical Center in Dallas

THERAPEUTIC

EXPERIENCE:

· Oncology/Hematology – Phase I – III – 3 years

· Prostate

· Lung

· Colon

· Breast

· Leukemia

· Infectious Disease – Phase II – III – 2 years

· HIV

· Ophthalmology – Phase – III – 1 years

· Macular Degeneration

· Cardiology – Phase II – III – 5 years

· Oral Thrombin Inhibitors

· Hypertension and CHF

· Device: cardiac, vascular stent, renal

· Respiratory – Phase II – III 4 years

· Cystic Fibrosis

· Chronic Bronchitis

· Allergy: SAR and PAR

· Renal – Phase II – III – 2 years

· Chronic Renal Failure Associated Disease – 1 year

· CRRT device – 1 year

· Multi Organ & Septic Shock – 2 years

· Acute Care: DIC – Phase III – 1 year

· Chronic Pain/Narcotic – 1 year

· Biologics: RA/OA – 2 years

· Biologics: anticoagulation – 1 year

· Gastrointestinal – Phase I 2 year

PROFESSIONAL

EXPERIENCE:

Owner: CRA Services, LLC (formed June 2011) - present

CRA Services (sole proprietorship)/ Cedar Hill, Texas

June 2002 – June 2011

C RA CONSULTANT (Senior Level - Contract)

· Conduct pre-study through close-out monitoring visits

· Site recruitment as requested

· Assure compliance with all GCP, ICH, SOP, and sponsor guidelines

· Responsible for site management, communication, and follow up

· Therapeutic Areas: Medical Devices – Cardiac assist, vascular stent, renal

Biologics – RA, sepsis, DIC, macular degeneration

Pharmaceuticals – pain, HIV, hypertension, CHF, oncology, bronchitis, allergy

AMGEN INC. /KFORCE ALLIANCE, Tampa, Florida

October 2000 to July 2002

Regional Clinical Research Consultant (Contract), Dallas, Texas

· Conducted pre-study through close-out monitoring visits

· Assured compliance with all GCP, ICH, SOP, and sponsor guidelines

· Responsible for site management, communication, and follow up

· Mentored new monitors

· Performed site recruitment activities for the alliance program

· Therapeutic areas: oncology, nephrology, dialysis, rheumatoid arthritis, hematology, cardiovascular and peri-surgery. Phases II – III

NOVARTIS PHARMACEUTICALS – East Hanover, New Jersey

January 2000 – October 2000

Regional Clinical Research Associate, Dallas, Texas

· Conducted pre-study through close-out monitoring visits

· Assured compliance with all GCP, ICH, SOP, and company guidelines

· Responsible for site management, communication, and follow up

· Performed site recruitment activities

· Therapeutic areas: Leukemia, CNS, dermatology and cardiovascular; Phases I-III. Adult and pediatric

DUPONT PHARMCEUTICALS, Wilmington, Delaware

July 1998 to January 2000

Regional Clinical Research Scientist, Dallas, Texas

· Conducted pre-study through close-out monitoring visits

· Assured compliance with all GCP, ICH, SOP, and sponsor guidelines

· Responsible for site management, communication, and follow up

· Performed site recruitment activities

· Therapeutic Areas: HIV, cardiology (thrombin inhibitor, peripheral vascular disease), pulmonary (chronic bronchitis, cystic fibrosis)

Senior Clinical Research Nurse

HIV/AIDS and Infectious Diseases

Univ. of Texas Southwestern Medical Center, Dallas, Texas

December 1993 - July 1998

Responsibilities: Executing clinical trials with HIV+ individuals. Experience with protocols from many pharmaceutical companies. Duties ranged from client visits with specimen collection and lab processing activities to IRB communications and maintenance of regulatory documents. Supervised professional and non-professional staff. Phases II – IV.

S taff Nurse (PRN) Intensive Care Unit

St. Paul Medical Center and Zale Lipshy Hospital, Dallas, Texas

March 1991 – November 2000

Responsibilities: Provide direct patient care to critically ill persons in these therapeutic areas: general medicine, neurology, neurosurgery, cardiology, cardiovascular surgery, thoracic surgery, general surgery, heart and lung transplantation. Cross-trained to Coronary Care Unit and General Medicine ICU.Served as charge nurse and as a clinical preceptor for new nurses and staff.

Дата добавления: 2015-11-13