Research Study Coordinator Senior
Listed on 2026-07-01
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Healthcare
Clinical Research
Job Summary
Coordinates & completes the day to day administrative & technical activities involved in a single complex, large, nationwide or multiple moderately complex concurrent biomedical &/or social‑behavioral research study(ies) involving multiple sites & /or longitudinal assessments/ interventions. Ensures that all activities are completed 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).
Department: MED-Obstetrics & Gynecology
Salary/Grade: NEX/13
Specific Responsibilities Technical- Participates in the planning & conduct of research studies.
- Reviews project & protocol & recommends strategies to expedite study.
- Recruits & retains participants.
- Obtains informed consent.
- Administers tests &/or questionnaires following protocols.
- Collects, compiles, tabulates &/or process responses.
- Gathers information.
- Extracts & analyzes data from medical charts.
- Completes basic clinical procedures such as drawing blood & obtaining blood pressure.
- Monitors & maintains systems for effective participant and data flow for studies.
- Designs & constructs experimental stimuli.
- Performs physical function assessment.
- Manages study databases which may include ensuring that data is collected & entered correctly.
- Reviews & analyzes data.
- Creates computer models, graphs, reports & summaries for use in publications, professional journals, & grant applications.
- Writes portions of grant applications.
- Co‑authors scientific papers for presentation & publication.
- Researches & obtains funding.
- Creates & maintains study manuals regarding operating, safety, and etc. procedures.
- Ensures that all study documents associated with current local, state, & federal regulatory guidelines, requirements, laws & research protocols are completed in a timely manner.
- May process payments for research participants per study protocol.
- Creates lab financial plan & budget/audit expenses.
- Obtains sales quotes for lab equipment & supplies.
- Reviews & adjusts expenses to decrease costs.
- Oversees repair & maintenance of all lab equipment & ensures that lab supplies are ready & available when necessary.
- Administers budget including negotiating with grant sponsors.
- Maintains & reconciles expenditures & balances in regard to research accounts & budgets.
- Trains, directs, assigns duties to & may supervise research staff, students, residents &/or fellows.
- Acts as a mentor in regard to education of junior coordinators.
Performs other duties as assigned.
Minimum Qualifications- Successful completion of a full 4‑year course of study in an accredited college or university leading to a bachelor's or higher degree in a major such as social or health science or related; OR appropriate combination of education and experience and 4 years' research study or other relevant experience required; OR
- Successful completion of a full course of study in an accredited college or university leading to a master's or higher degree in a major such as social or health science or related; OR appropriate combination of education and experience and 2 years' research study or other relevant experience.
- Must complete NU's IRB CITI training before interacting with any participants & must re‑certify every 3 years.
Target hiring range for this position will be between $23.94 - $28.99 per hour. Offered salary will be determined by the applicant’s education, experience, knowledge, skills and abilities, as well as internal equity and alignment with market data.
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