layiq

/la·yiq/adjective

worthy; deserving; fitting; suitable.

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

Clinical Research Manager - Hematology and Oncology at University of Chicago | LAYIQ

Directs a program or research office.
Conducts research in 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 applications of technology.
Establishes goals and operating procedures, practices, and guidelines.
Establishes, monitors, and controls project budgets.
In collaboration with research faculty and personnel, participates as a skilled individual contributor and/or researcher.
Prepares grant/funding applications.
Manages financial, personnel, planning, compliance and other administrative aspects of research project(s).
Oversees activities related to data collection and analysis.
Coordinates the conduct of the study from screening to completion, including recruitment and screening of study subjects, obtaining informed consent, collecting research data, and ensuring protocol adherence.
Protects patients and data confidentiality by ensuring security of research data and personal health information.
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.
Supervises both researchers and research support staff.
Plans and manages the protocol review process for all clinical trials which includes the receipt and coordination of protocols for review, committee meetings, and clinical research 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.
Performs other related work as needed.

Clinical Research Manager - Hematology and Oncology

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