Title: Senior Research Data Coordinator

Company: Abbott Laboratories

Location: Abbott Park, IL

Salary: commensurate with experience

Job Description:

Follow your aspirations to Abbott for diverse opportunities, competitive salaries, great benefits, a 401(k) retirement savings plan, a company paid pension plan and profit sharing, all with a company providing the growth and strength to build your future.

Description:
Designs, reviews and approves CRFs to ensure that they accurately reflect the protocol. Creates, reviews, and approves QA plans. Performs, coordinates and ensures that QA processes are implemented following study QA plans. Major Responsibilities: Responsible for implementing and maintaining the effectiveness of the quality system. Ensures that CRF design supports database structure. Designs, reviews, and approves study databases to ensure that they accurately reflect the CRFs. Designs, maintains, reviews, and approves edit check specifications to ensure that the checks reflect the QA plan. Maintains, reviews, and approves documentation to ensure that documentation reflects both the historical and current status of studies.

Qualifications:
Follows both project and department standards. Incorporates review feedback appropriately. Oracle Clinical Data Management experience strongly preferred, attention to detail, strong written and verbal communication skills, multitasking ability. Must have at least 4 years experience in Clinical Data Management. BA/BS (prefered Life Science/Computer Science or Health related)

Abbott welcomes and encourages diversity in our workforce. EEO/AA

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