layiq

/la·yiq/adjective

worthy; deserving; fitting; suitable.

A role, opportunity, or path that merits attention, time, and pursuit.

Clinical Research Manager at University of Chicago | LAYIQ

Research Conduct/Study Management: Responsible for the direction of a program or research office.
Conducts research in the area of expertise.
Collaborates with other researchers on long-range plans for research projects.
Oversees the development of research projects.
Ensures research projects progress according to plan.
Investigates, modifies, and applies new procedures, techniques, or technological applications.
Establishes goals and operating procedures, practices, and guidelines.
Establishes, monitors, and controls project budgets.
In collaboration with senior research faculty and personnel, participates as a skilled individual contributor and/or lead researcher as an expert in a specialized area.
Prepares grant/funding applications.
Manages financial, personnel, planning, compliance, and other administrative aspects of research project(s).
Data Management: Oversees activities related to data collection and analysis.
Coordinates the conduct of the study from screening through to completion, including recruitment and screening of study subjects, obtaining informed consent, collecting research data, and ensuring protocol adherence.
Protects patient and data confidentiality by ensuring the security of research data and personal health information.
Regulatory: Ensures compliance of research activities with institutional, state, and federal regulatory policies, procedures, directives, and mandates.
Understands the IRB submission and review process and when and how to apply for IRB review, including facilitation of study initiation through meticulous and timely preparation of IRB submissions.
Understands the federal research regulations and identifies the federal research organizations’ role in regulating human research participation.
Identifies and explains the responsibilities of Principal Investigators, research team members, sponsors, contract research organizations (CROs), and regulatory authorities related to the conduct of a clinical trial.
Writes articles, reports, and manuscripts and presents research findings at meetings and/or conferences.
Advises the development of a formalized training program for both new and existing staff within the unit and any affiliates and/or partners. Monitors federal regulatory agency requirements related to clinical research training requirements and ensures training activities comply with requirements.
Manages PI and other senior research faculty and personnel, participates as a skilled individual contributor and/or lead researcher as expert in specialized area. Ensures research projects progress according to plan by overseeing the coordination of the daily clinical trial activities.
Performs other related work as needed.

Clinical Research Manager

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Employer job description

About the Department

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Preferred Qualifications

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Benefits Eligible

About this listing

Salary