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Sales Representative Coordinator

Location:
Chesterfield, MO, 63005
Posted:
March 09, 2010

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Resume:

Curriculum Vitae

Marsha A. Ponzar

Home: 636-***-****

Office: 636-***-****

CURRENT POSITION

Omnicare Clinical Research, Chesterfield, MO., USA 2007-2009

Clinical Research Associate/ CRA

Responsibilities include:

Identification of potential investigational sites

Coordinates and performs comprehensive site management

Conduct pre-study, initiation, interim and close out monitoring visits

Produce comprehensive visit reports and status reports

Resolve data issues and audit issues

Adhere to the study timelines and budget

Collect high quality critical documents and completion of ethics

committee and regulatory submissions in association with Investigator Services.

PROFESSIONAL EXPERIENCE

St. Luke’s Hospital, Chesterfield, MO, USA 2006-2006

Clinical Research Coordinator

Responsibilities included:

Adhered to Good Clinical Practices, Standard Operating Procedures and Study Protocols

Prepared informed consent documents and case report forms

Monitored monthly and bimonthly CALGB, NSABP, and CTSU bulletins for protocol changes,

study specific adverse events and consent revision changes

Rewrote study consent documents to reflect necessary changes made in increased risks to

participants and protocol changes

Prepared appropriate study specific regulatory submissions to the IRB that may include

expedited or full review applications, SAEs, protocol changes, consent changes, study

closure notices and other relevant IRB submissions

Determined patient eligibility for study enrollment and obtaining informed consent from study

participant

Constructed a calendar of required tests and treatment/follow up visits for the patient’s office

chart and made the appropriate form submissions based on protocol requirements

Collected and maintained supporting source documentation

Washington University School of Medicine, St. Louis, MO, USA 2002 - 2005

Clinical Research Coordinator/CRA (Department of Orthopedic Surgery)

Responsibilities included:

Responsible for patient recruitment and enrollment as well as managing cohort follow-ups

Screened 65/70 Clinic patients per week for initial study enrollment and follow up data

Maintained site documentation and filed paperwork submissions for IRB review

Coauthor/contributor on six abstracts

Medical Assistant for monthly Fellow’s Clinic

Assisted Residents in their research rotation responsibilities

Responsible for entering all surgeries into a database and maintaining it

Department of Internal Medicine - Home based CRA

Team leader in continued development and revision of study protocol used by the three

research centers (Washington University, Harvard University and the University of

Maryland)

Trained research personnel in proper data acquisition and retention

Recruited nursing home owners/managers to participate in the research study

Enlisted the enthusiastic participation of nursing home Directors of Nursing and related

institutional staff in the conceptual structure and implementation of study protocols and

research objectives

Integrated research protocols and processes with nursing home staff functions to assure

mutual satisfaction in achieving research goals with least negative effect on efficiency

Screened, selected (including administering psychometric tests), and educated patients for

participation in the study

Rounded on patients and monitored for compliance and any possible adverse affects

K.V. Pharmaceutical Co. (Ethex), St. Louis, MO, USA 1999- 2001

Sales Representative

Responsibilities included:

Delivered consistently strong sales result in promoting and marketing ethical pharmaceuticals

in key market segments: Physicians, chain and independent pharmacies

Strong customer advocate assuring satisfaction with products, distribution, and marketing

practices

Broadened pharmacists` knowledge of company products and services, thus expanding

market penetration

Successfully prospected for new clients and emerging market segments

Developed territory accounts to maximize the sale and exposure of the product line

THERAPEUTIC EXPERIENCE

Therapeutic Categories Specialized Area(s) Phase(s) Role(s)/Year(s) of Experience

Endocrinology and Metabolism Obesity Phase III Clinical Study Coordinator: 2 Month(s)

Oncology/Gastroenterology Colon Malignancies Phase III Clinical Study Coordinator: 1 Year

Oncology/Genitourinary Disorders Colon/Rectal Cancer Phase III Clinical Study

Coordinator/CRA: 1 Year

Oncology/Genitourinary Prostate Cancer/Phase II CALGB Clinical Study Coordinator/1 Year

Oncology/Gynecology Carcinoma - Breast Phase III Clinical Study Coordinator/CRA: 1 Year

Internal Medicine Obesity Studies Phase III Clinical Study Coordinator: 2 Month(s)

Musculoskeletal Hip-Knee Replacement Phase IV Clinical Study Coordinator: 1 Year

Musculoskeletal Orthopedics Phase IV Clinical Study Coordinator/CRA: 1 Year

Musculoskeletal Rheumatoid Arthritis Phase IV Clinical Study Coordinator: 1 Year

Musculoskeletal Back Pain Phase IIIB /CRA: 2 years

Neurology Dementia Phase IV Clinical Study Coordinator/CRA: 1 Year

Neurology Disorders of Neuromuscular Transmission Phase IV Clinical Study Pediatric

Coordinator/CRA: 1 Year

Rheumatology Phase IV Clinical Study Coordinator/CRA: 1 Year

Psychiatry Alzheimer's disease Phase IV Clinical Study Coordinator/CRA: 1 Year(s) -

Psychiatry Dementia Phase IV Clinical Study Coordinator/CRA: 1 Year

Psychiatry Depression -Adult Phase IIIB/CRA 3 months

EDUCATION

Washington University, College of Arts and Sciences, St. Louis, MO, USA

BA, Biology

ADDITIONAL EDUCATIONAL DETAILS

Computer Skills:

Microsoft Access

Excel

PowerPoint

Outlook

Microsoft Word

IDX

Mediscribe

Clinical Desktop

Sales Logix

WebPins

Seminars/Course Work:

Completion of CRA and IRB training, Washington University

Completion Certificate for the Human Participants Protection Education for Research Teams,

renewed yearly and current

HIPAA Compliance Training

Electronic data capture experience (E-Trials) in addition to a Phase Forward Inform 4.5 course

completion certificate.

PROFESSIONAL AFFILIATIONS

ACRP, Member

PUBLICATIONS/PRESENTATIONS

John C. Clohisy, MD, James A. Keeney, MD, Marsha Ponzar, BA, Perry L. Schoenecker, MD. A

Treatment Algorithm for Hip Disorders in Patients 50 Years Old and Younger, 2005;

John C. Clohisy, MD, Ryan Nunley, MD, Madelyn Curry, RN, Marsha Ponzar, BA, Perry L.

Schoenecker, MD. Periacetabular Osteotomy for the Treatment of Perthes-Like Deformities of the

Hip, 2005;

Stephen Burnett, MD, FRCS (C), Marsha Ponzar, BA. Acetabular Labral Tears, 2005;

Stephen Burnett, MD, FRCS (C), Marsha Ponzar, BA. Revision Total Knee Arthroplasty in

Patients That Have Undergone a Tibia Tubercle Osteotomy, 2005;

John C. Clohisy, MD, Thomas McClure, MD, Jason Robison, MD, Marsha Ponzar, BA. Treatment

of Anterior Femoroacetabular Impingement with Combined Hip Arthroscopy and Limited Open

Osteoplasty, 2005;

Ryan C. Chen, MD, John C. Clohisy, MD, Marsha Ponzar, RN. Hip Arthroscopy in Patients Older

than 45 Years, 2005;



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