The Senior Data Assistant serves as a resource to staff regarding data entry, maintenance, and results. This role coordinates incoming data for accuracy and integrity, assists with complex data preparation, analyzes data, and creates reports. This position ensures associated administrative tasks such as documentation, editing of code books and manuals, etc. are completed.
The Data Assistant Sr. is responsible for the compilation of all data for clinical trials managed by the CTO.
Partners with internal/external project and IT staff to create, review, analyze, interpret, summarize and prepare progress and final reports.
Provides consultation to internal/external project staff on appropriate data management, methodological issues and analysis of data.
Identifies and assesses customer data needs.
Assists in identifying organizational area's data integration and related records solutions.
Collaborates on a variety of data management projects including variable definitions, storage, etc.
Obtain required training for all electronic data capture systems.
Obtains applicable protocol specific training.
Abstract all required patient data from medical record sources for entry into case report forms (paper and/or electronic).
Follow timelines stated in SOP (CO-SM-312) and individual sponsor contracts, for data entry and query resolution.
Seek out data by contacting other hospitals and physician offices to obtain medical records as needed.
Main contact for monitors/CRO’s for data query resolution.
Responsible for the long term follow-up with patients who are no longer receiving active treatment which may involve direct contact with patients, their families and/or referring physicians.
Responds to sponsor/CRO data concerns and escalates issues to management as appropriate.
Ensures that all data is obtained and verified for subsequent analysis.
Provides updates and summaries regarding statistics.
Provides administrative support to organizational area.
Attend mandatory scheduled meetings
Increase knowledge of all disease specific oncology studies to ensure efficient data abstraction and resolution of queries.
Assesses protocol compliance and communicates directly with the study coordinator and PI when compliance issues are identified.
Assist with all internal audit request.
Gives input on CTO policies and procedures with regards to data entry/monitoring.
Writes queries and reports and creates necessary analysis.
Schedule and participate in all monitor visits for assigned studies.
Facilitate EMR access for monitors.
Resolve issues noted in follow up letter within 3 weeks.
Assists with any sponsor audit requests
Runs and distributes standard scheduled reports.
Maintains and updates report inventory.
Archives complex data structures to prepare final catalog of data sets.
Performs advanced cleaning/formatting tasks of datasets.
Assists in mentoring/training entry level data assistants.
Performs other duties as assigned.
A high school diploma or equivalent is required.
4 years' data entry or similar experience is required.
Please see information highlighted below
Enterprise Applications: EIACUC, eIRB, Kronos.
Infrastructure: Microsoft Lync, Microsoft Office (Word, Excel, Powerpoint, Access, Outlook, Microsoft SharePoint.
Compliance: FDA GLP, HIPAA
Analytical: Critical thinking, decision making, problem solving, troubleshooting.
Minimum Competencies: (Skills, knowledge, and abilities.)
Ability to understand complex pathology data and cancer treatment regimens and their toxicity
Ability to establish and maintain effective working relationships with patients, physicians, nurses, technicians and co-workers.
Excellent verbal and written communication
Preferred Qualifications: (Education and experience)
Bachelor’s degree in the health sciences, social sciences, or advertising/marketing.
Experience in data management in a health field, exposure to cancer clinical trials.
Computer literate in basic software, internet use, and cancer-related databases.
At least 1 year of work experience in a customer service oriented position.
1-2 years’ experience in cancer research
1-2 years’ experience in Clinical Trials
Preferred Competencies: (Skills, knowledge, and abilities)
Prior administrative or public responsibility desirable
Experience in data management in a health field
Exposure to cancer clinical trials
Communication – Oral and Written
As per Northwestern University policy, this position requires a criminal background check. Successful applicants will need to submit to a criminal background check prior to employment.
Northwestern University is an Equal Opportunity, Affirmative Action Employer of all protected classes, including veterans and individuals with disabilities. Women, racial and ethnic minorities, individuals with disabilities, and veterans are encouraged to apply. Hiring is contingent upon eligibility to work in the United States.
Northwestern University is a major private research university with 12 academic divisions located on three campuses in Evanston, Chicago, and Education City in Doha, Qatar. We have approximately 2,500 full-time faculty members, 17,000 graduate and undergraduate students, and over 5,700 full and part-time staff. Northwestern University combines innovative teaching and pioneering research in a highl...y collaborative environment. It provides students and faculty exceptional opportunities for intellectual, personal and professional growth.