Clinical Research Data Entry

Deona Lowman

**** ****** ******

Philadelphia, PA, 19124

Summary

. Over 10 years of experience working in clinical research

. Over 8 years of experience working for ICON Clinical Research

. Clinical Research Therapeutic Areas include:

Cardiovascular

Heart Disease

Heart Failure

Infections and Infestations

Vaccines

Renal and Urinary Disorders

Renal Failure

Renal Insufficiency

Neoplasms Benign, Malignant and Unspecified

Bladder Cancer

Breast Cancer

Prostate Cancer

Ovarian Cancer

. Systems/Computer skills include: Word, Excel, Access, Oracle Clinical,

Medidata RAVE, SAS, OCRDC

. Experience in Electronic Data Capture trials: OCRDC, eCaseLinks,

Medidata RAVE

. Languages : English (verbal and written)

Professional Experience

ICON Clinical Research Reconciled safety and local lab data in accordance

Clinical Data Coordinator II to applicable procedures.

January 2008 to Present Assisted in the development of Data Management

study specific procedures.

Developed a more efficient way of addressing

outstanding data queries.

Assumed study lead role's responsibilities when

applicable.

Represented Data Management at internal/external

meetings as appropriate.

Effectively mentored and trained less experienced

staff.

ICON Clinical Research Independently and accurately reviewed all data

Clinical Data Coordinator I discrepancies.

August 2006 to January 2008 Performed quality review checks on several

studies.

Reviewed case report form data for accuracy and

consistency.

Maintained study files electronically and

manually.

Cephalon Performed User Acceptance Testing on various

Clinical Data Quality studies as requested.

Specialist Compared SAS reports to clinical databases to

March 2003 to August 2006 resolve data issues.

Created data entry guidelines and folders for

study start-up.

Logged case report forms, EKG's, labs and queries

into Clintrial database.

First Lab, Inc. Scheduled drug screening appointments for business

Assistant Account Specialist clients.

February 2003 to March 2003 Completed client requests through contact of

various lab facilities.

Logged donor's medical data into tracking system

and retrieved status of donor's specimen.

Prepared and mailed drug screening forms via

Federal Express to donor's address or lab

facility.

GlaxoSmithkline Managed study files in the clinical file room.

Data Entry Specialist Scheduled data entry staff's time to oversee the

April 1997 to June 2001 clinical file room.

Assisted in the training of new data entry

personnel.

Created reports, files and other documents for

data entry manager.

Maintained a weekly and monthly log of data entry

staff's productivity.

Education

Computer Learning Center

Certificate in Computer Operations

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