Resume

Sign in

Clinical Research Coordinator

Location:
Gurnee, Illinois, United States
Posted:
March 13, 2019

Contact this candidate

Resume:

DOROTHY ZAKULA

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

Gurnee, IL 60031 ac8rtw@r.postjobfree.com

SUMMARY OF QUALIFICATIONS

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

PROFESSIONAL EXPERIENCE

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

Analysis

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

Administration

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

EMPLOYMENT HISTORY

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

EDUCATION

Northern Illinois University—DeKalb, IL

Bachelor of Science in Biological Sciences, May 1986

Minor: Chemistry

Cumulative GPA: 3.2/4.0

COMPUTER PROFICIENCY

Microsoft Word

Microsoft Excel

Microsoft PowerPoint

Microsoft Outlook

Oracle Clinical

Medidata Rave

Data Entry



Contact this candidate