- Researches and collects data through site or home visit intakes; library research; structured interviews; or through other means for research projects. 2. Interprets, synthesizes, and analyzes data using scientific or statistical techniques. Modifies and plans research experiments, procedures, tests, or survey instruments. Assists in research design. 3. Writes and edits material for publication and presentation. Reports on status of research activities. Oversees and instructs research and support staff on technical procedures, equipment operation, and laboratory maintenance. 4. Schedules and coordinates research activities. Identifies and recruits study participants. Orders and maintains inventory of supplies. 5. May assist in preparing financial information and monitoring budgets. 6. Performs additional functions incidental to research activities.
Required Education and Experience
Two years of related work experience in the same job family and a Bachelor's degree in a related field; or an equivalent combination of experience and education.
Background Check Requirements
All candidates for employment will be subject to pre-employment background screening for this position, which may include motor vehicle, DOT certification, drug testing and credit checks based on the position description and job requirements. All offers are contingent upon the successful completion of the background check. Please visit www.yale.edu/hronline/careers/screening/faqs.html for additional information on the background check requirements and process.
The Yale Center for Clinical Investigation, is seeking a detail-oriented, full-time clinical research assistant who enjoys working with data. Responsibilities for this position will include but not be limited to:
Work with OnCore, the university's Clinical Trials Management System, as well as EDC, to develop and maintain study participant activity and biospecimen tracking. Build and/or assist with study specifications for electronic case report forms (eCRFs) in REDCap for clinical data collection. Organize, enter, and monitor information for effective data management in OnCore, REDCap and other electronic data capture systems for clinical trials. Register and manage data from study participants throughout the lifecycle of clinical studies and registries. Collect, process, track/store and ship biospecimens.
Work in collaboration with researchers and Clinical Research Coordinators to assist in the initial submission and required edits/amendments to research protocols, informed consent forms, and work with the Office of Sponsored Projects, Yale Center for Clinical Investigation, and Yale's Institutional Review Board to receive approval for clinical studies.
Preferred Education, Experience and Skills:
Prior experience performing data management tasks. Experience with EPIC or other EMR system.
The intent of this job description is to provide a representative summary of the essential functions that will be required of the position and should not be construed as a declaration of specific duties and responsibilities of the particular position. Employees will be assigned specific job-related duties through their hiring departments.
Affirmative Action Statement:
Yale University considers applicants for employment without regard to, and does not discriminate on the basis of, an individual's sex, race, color, religion, age, disability, status as a veteran, or national or ethnic origin; nor does Yale discriminate on the basis of sexual orientation or gender identity or expression. Title IX of the Education Amendments of 1972 protects people from sex discrimination in educational programs and activities at institutions that receive federal financial assistance. Questions regarding Title IX may be referred to the University's Title IX Coordinator, at TitleIX@yale.edu, or to the U.S. Department of Education, Office for Civil Rights, 8th Floor, Five Post Office Square, Boston MA 02109-3921. Telephone: 617.289.0111, Fax: 617.289.0150, TDD: 800.877.8339, or Email: email@example.com.