SMART Project Research Study Coordinator

This position coordinates collection, analysis, processing & reporting of data & assists Principal Investigator (PI) in judging the validity of test data obtained in regard to biomedical &/or social-behavioral research study(ies) of limited complexity involving co-investigators, multiple campuses &/or universities. The Research Study Coordinator completes all activities by strictly following Good Clinical Practices (GCP) & all relevant current local, state, & federal laws, regulations, guidance, policy & procedure developed by the NU Institutional Review Board (IRB), Food & Drug Administration (FDA) Code of Federal Regulations (CFR), & the International Conference on Harmonization (ICH). Continue Reading ▶︎

Postdoctoral Scholar in Sexual Minority Couples’ Health and HIV Prevention

The IMPACT LGBT Health and Development Program within the Northwestern Institute for Sexual and Gender Minority Health and Wellbeing (ISGMH) seeks a post-doc to be involved in two randomized controlled trials of 2GETHER–a relationship education and HIV prevention program for young male couples. Research activities include project-related activities (e.g., facilitating sessions), authoring and co-authoring manuscripts, analysis of existing data, and collaborating on ongoing projects. Continue Reading ▶︎

CONNECT/EDIT Data Assistant Associate

Job Summary: Collects, reviews, verifies, validates, codes and inputs data into a computer processing system; audits output data. Identifies and resolves production related errors. Maintains and revises procedural lists, control records and coding schemes to process source data. Assists with the management and coordination of connections with program and study partners. Continue Reading ▶︎

SMART Project Research Study Assistant #31376

The Research Study Assistant performs biomedical and/or social-behavioral research by administering tests and/or questionnaires following protocols; collecting, compiling, tabulating and/or processing responses; gathering information; and/or assisting in the preparation of material for inclusion in reports. Completes all activities by strictly following Good Clinical Practices (GCP) and all relevant current local, state, and federal laws, regulations, guidance, policy and procedure developed by the NU Institutional Review Board (IRB), Food and Drug Administration (FDA) Code of Federal Regulations (CFR), and the International Conference on Harmonization (ICH). Continue Reading ▶︎

SMART Project Research Study Assistant #31377

The Research Study Assistant performs biomedical and/or social-behavioral research by administering tests and/or questionnaires following protocols; collecting, compiling, tabulating and/or processing responses; gathering information; and/or assisting in the preparation of material for inclusion in reports.  This role completes all activities by strictly following Good Clinical Practices (GCP) and all relevant current local, state, and federal laws, regulations, guidance, policy and procedure developed by the NU Institutional Review Board (IRB), Food and Drug Administration (FDA) Code of Federal Regulations (CFR), and the International Conference on Harmonization (ICH). Continue Reading ▶︎

Grant Writer

Reporting to the associate director, the grant writer is responsible for raising financial support from funders requiring proposals, both for unrestricted and restricted revenue. The candidate should have a proven track record in producing successful grant proposals.

Primary Duties and Responsibilities: