at Northwestern University in Evanston, Illinois, United States
Job Description
Job Opening Id: 49861
Department: MED-Endocrinology
Salary/Grade: RES/
Job Summary:
The Division of Endocrinology is seeking a full-time Clinical Research Associate for an exciting, expanded role in cutting-edge diabetes research. This position is 100% supported by funding from federal and non-profit organizations, under the supervision of Dr. Amisha Wallia.
The Clinical Research Associate role will be responsible for managing research-related activities for both epidemiological and novel interventional studies in diabetes (Type 1, with opportunities in Type 2), Under direction of the PI, assists in performing biomedical research. This may involve recruiting subjects for studies, preparation and submission of IRB regulatory materials, preparation and submission of OSR documents, administering tests &/or questionnaires; collecting, compiling, tabulating &/or processing responses; gathering information; &/or assisting in the preparation of material for inclusion in reports.The candidate will need to ensure that all study activities are completed by strictly following Good Clinical Practices (GCP) and all current local, state, and federal laws, regulations, guidance, policy & procedure developed by the Northwestern University Institutional Review Board (IRB), Food and Drug Administration (FDA) Code of Federal Regulations (CFR), and the International Conference on Harmonization (ICH).
This hybrid position is located on the Northwestern University Chicago Campus with one day per week remote or flexible hours. Please include a cover letter detailing relevant experience and interest with clinical research.
Please note: Working environment may include an ambulatory clinic &/or hospital setting.
Specific Responsibilities:
- Recruits research subjects for clinical studies; provides list to check in area of subjects who will be coming in that day; may bring subjects into exam rooms; Provides all necessary support during studies. May administer informed consent.
- Assists PI and other investigators in preparation and submission of IRB regulatory materials, preparation and submission of OSR documents (including consent forms), maintenance of records according to all regulations.
- Assists research coordinator in collecting, compiling, tabulating &/or processing responses; gathering information; &/or assisting in the preparation of material for inclusion in reports and journals. Assists with submission to journals.
- Ass
