Clinical Research Manager - Hematology and Oncology
$90,000–$130,000 year
On-siteChicago, Illinois, United States
Job Summary
Direct a research program or office by overseeing project development, budget management, and compliance with institutional and federal regulations. Coordinate study conduct from screening to completion, including recruitment, informed consent, and data collection while ensuring protocol adherence. Supervise clinical research coordinators and researchers, manage training programs, and facilitate IRB submissions. Collaborate with principal investigators, sponsors, and CROs to lead protocol reviews and ensure regulatory policy compliance. Prepare grant applications and analyze program performance to drive strategic research initiatives within the Hematology/Oncology department.
Required Qualifications
- college or university degree in related field
- 7+ years of work experience in a related job discipline
- Drug Test Required
- Health Screen Required
Desired Qualifications
- Master's degree
- Supervisory skills
- Background in a leadership role
- Research certification, such as Graham School Clinical Trials Management and Regulatory Compliance, SoCRA, ACRP
- 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)
- Develop a program and a team
- Excellent time management skills and work independently
- Strong analytical skills
- Identify funding sources
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