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Clinical Research Coordinator

Gurnee, Illinois, United States
March 13, 2019

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**** ****** **** ****: 224-***-****

Gurnee, IL 60031


Data analysis responsibilities utilizing strong attention to detail and follow-through

Project management skill demonstrating skilled communication and teamwork

Exceptional record keeper, with emphasis on consistency and deadlines


Project Accomplishments

Granted Medidata Rave edc access to global customers including CRA’s, clinical site personnel and internal employees within 24 hours of receiving an email request

Assisted Rave users by providing technical support for any account related issues

Managed all clinical site administration which included the addition of confirmed sites to Rave and any updates to the site name or number

Created investigator and sponsor CD-ROM’s at the end of study for distribution to the clinical sites.

Supported department Data Managers in the submission of study documents to the Trial Master File repository

Coordinated internal Rave database audit to check for unauthorized users bi-annually and at study hard lock

Met assigned performance goals for complex testing and research, including performance feedback given directly from customers’ input

Collaborated with other technicians and scientists to complete eight screenings for Cancer Research

Conducted highly visible research project with outside company, coordinating all scheduling, meetings and timelines which resulted in four drug targets.

Excelled in a service team environment, oriented to the customer’s immediate project needs

Developed efficient schedule to double the amount of testing performed per week

Contributed to group meetings to outline project scope, schedules and deliverables to maximize productivity


Handled graphing, data analysis and presentation of complex screening results

Provided quality test results used to evaluate potential drug leads for multiple projects simultaneously

Contributed to valuable kinetic studies and screened purified protein samples using automation

Monitored scientific data accuracy and consistency to improve experimental outcome


Forecasted inventory needs and ordered appropriate cost effective supply levels to ensure seamless work

Coordinated scientific instrument use schedules with other employees for efficient time management

Recruited volunteers for special clinical studies to evaluate the feasibility of a new technology

Recognized for detailed recordkeeping abilities by providing thorough and consistent information for department

Proficient with many software programs and in-house computer systems to increase efficiency


Astellas Pharma Global Development; Northbrook, IL

2009-2019 Sr. Data Science Coordinator, Data Sciences Department

Astellas Pharma US, Inc.; Deerfield, IL

2008-2009 Data Verification Analyst (Contractor), Data Sciences Department

Advanced Clinical Research Services; Bannockburn, IL

2007-2008 Clinical Data Entry Operator

Abbott Laboratories; Abbott Park, IL

1990-2006 Associate Biochemist, Drug Discovery Research Division

1988-1990 Research and Development Technician, Diagnostics Division

Rosalind Franklin University of Medicine and Sciences; North Chicago, IL

1986-1988 Research Technician, Department of Biochemistry


Northern Illinois University—DeKalb, IL

Bachelor of Science in Biological Sciences, May 1986

Minor: Chemistry

Cumulative GPA: 3.2/4.0


Microsoft Word

Microsoft Excel

Microsoft PowerPoint

Microsoft Outlook

Oracle Clinical

Medidata Rave

Data Entry

Contact this candidate