- Location: Durham, NC
- Posted: May 17, 2019
Working 1st shift, 10am - 6:30pm
Maintain a variety of data used in support of analytical and/or research projects. Perform varied clerical duties in support of general and special office activities to maintain an efficient and effective operation.
Associates Degree, Preferred. At least three months of clerical or general office support experience to become familiar with activities involved in providing routine clerical support. Experience with computers / data entry desirable.
Work Performed:Completion of CIBMTR Data Entry forms
Completion of NMDP Data forms
Completion of Post-Infusion Data Forms for Cord Blood Banks (ie. CBR, Viacord, etc).
Pull laboratory files needs for audit/monitoring visits.
File laboratory files when monitoring visits are completed.
Lab Assistant-related duties, as appropriate, to include inventory and supply management.
Data Entry of Graft Characterization forms (CCBB EMMES Database)
Data Entry of Stem Cell and Infusion forms in STCL EMMES Database
Perform a variety of research, database, and clerical duties of a complex and technical nature in support of clinical trials.
Data management and informatics. Use Electronic Data Capture (EDC) systems, technologies, and software necessary for study operations. Enter data accurately. Complete paper and electronic Case Report Forms (CRFs and eCRFs) accurately and according to protocol. Assist with the development of data collection documents to standardize process. Detect issues related to data capture, collection or management; suggest solutions.
Investigate incomplete, inaccurate, or missing data/documents to ensure accuracy and completeness of data; follow and develop, or assist with development of, SOPs for data quality assurance. Adhere to processes and run queries, summaries, and reports to monitor the quality of data. May develop QA processes and oversee the creation and use of queries, summaries, and reports for quality assurance purposes. May be responsible for recognizing trends related to data quality and escalating as appropriate.
Work with Clinical Research Coordinators to enter outcomes data, as needed.
Perform all other job-related duties as requested by supervisory staff.
Attention to detail
Data entry experience
Excellent verbal and written communication skills
- FULL TIME