DirectJobHub
Jobs · Analyst · Illinois

Clinical Research Manager - Hematology and Oncology

University of Chicago · Chicago, IL · 1 wk ago
On-siteAnalyst$90k–$130k/yrOther

About the Department

The Section of Hematology/Oncology has a proud and long tradition of excellence in research-based patient care and clinical discovery. Ranked among the finest cancer programs in the country, the Section is comprised of nationally and internationally known faculty with expertise in all major types of malignancies, blood disorders, and experimental therapies.

About the Role

The Clinical Research Manager will provide project management, data management, and clinical monitoring support for multiple types of trials, including sponsored, grant-funded, multi-site, and/or investigator-initiated trials, in the Section of Hematology/Oncology in the Department of Medicine. The Clinical Research Manager will act as a liaison between clinical sites, the Clinical Trials Office, and sponsors/agencies to ensure that clinical trials are conducted in compliance with the protocol and applicable institutional and regulatory guidelines. They will also provide day-to-day project oversight and management to the Clinical Research Coordinators.

Responsibilities

  • 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.

Requirements

  • Minimum requirements include a college or university degree in a related field.
  • Minimum requirements include knowledge and skills developed through 7+ years of work experience in a related job discipline.

Qualifications

  • Preferred Education: Master's degree.
  • Preferred Experience: Supervisory skills and background in a leadership role.
  • Preferred Certifications: Research certification, such as Graham School Clinical Trials Management and Regulatory Compliance, SoCRA, ACRP.
  • Technical Skills or Knowledge:
    • Proficient in monitoring and auditing clinical research trials for compliance/billing accuracy, such as site monitoring, quality assurance, and creating monitoring plans.
    • Working knowledge of managing research projects.
    • Develop research program and work strategically with principal investigator(s).
    • Lead robust operational and financial analysis of study(ies) and/or program performance.
    • Read and understand clinical trials protocols.
    • Knowledge of regulatory policies and procedures.
    • Knowledge of grant and contract administration.
    • Familiarity with medical and scientific terminology.
    • Demonstrated knowledge of Good Clinical Practices (GCP).
  • Preferred Competencies:
    • Develop a program and a team.
    • Excellent time management skills and work independently.
    • Strong analytical skills.
    • Identify funding sources.

Benefits

The University of Chicago offers a wide range of benefits programs and resources for eligible employees, including health, retirement, and paid time off. Information about the benefit offerings can be found in the Benefits Guidebook.

Pay

The pay range for this role is $90,000.00 - $130,000.00.

Similar jobs