Clinical Team Supervisor

Universities of Wisconsin • Madison, WI

1d • $70,000 • Hybrid

About The Position

The Myeloma Clinical Team Supervisor will function on the management team of the myeloma clinical research program within the Clinical Research Central Office (CRCO) at the University of Wisconsin Carbone Cancer Center (UWCCC). Under the direction of the Clinical Team Manager, the incumbent will directly supervise, mentor and train Clinical Research Coordinators, ensuring that all research activity adheres to applicable International, Federal, State, and Institutional laws, policies, procedures and requirements. The Supervisor will serve as a Clinical Research Coordinator, managing a large patient load in addition to their supervisory duties. The incumbent must be able to handle multiple projects simultaneously and work independently using initiative and good judgment, serving as a leader on the team. This position may require some work to be performed in-person, onsite, at a designated campus work location. Some work may be performed remotely, at an offsite, non-campus work location. This position has been identified as a position of trust with access to vulnerable populations. The selected candidate will be required to pass an initial caregiver check to be eligible for employment under the Wisconsin Caregiver Law and every four years. Our mission is a commitment to defeating cancer through rapid application of groundbreaking research, prevention, and treatment. The University of Wisconsin (UW) Carbone Cancer Center has been an NCI-Designated Comprehensive Cancer Center since 1973. UW Carbone is an integral part of the UW School of Medicine and Public Health and UW Health, bringing together more than 330 physicians and scientists from 50 departments and nine schools to conduct research and translate laboratory discoveries into new patient treatments. UWCCC builds community by creating a collaborative, respectful, and welcoming environment in which all faculty, students, and staff will thrive.

Requirements

• Minimum 2 years of experience coordinating clinical trials in hematologic malignancies
• SOCRA - Certification in Clinical Research required to be obtained within 6 months of hire

Nice To Haves

• Experience with multiple myeloma

Responsibilities

• Schedules logistics and secures resources for a defined clinical research trial of high complexity and/or multiple research trials
• Monitors program budgets and approves unit expenditures
• Exercises supervisory authority, including hiring, transferring, suspending, promoting, managing conduct and performance, discharging, assigning, rewarding, disciplining, and/or approving hours worked of at least 2.0 full-time equivalent (FTE) employees
• Collects, prepares, processes, analyzes, and submits participant data and samples to appropriate entities, adhering to research protocols and compliance with applicable policies and procedures
• Assists with review of current research trials, development of operational protocols and work unit policies, and makes recommendations to leadership for improvements
• Composes, assembles, and submits grant proposals and study protocols according to applicable rules and regulations
• Serves as a subject matter expert and main point of contact for clinical research participants providing information regarding research procedures, expectations, and informational inquiries
• Recruits, screens, and enrolls trial participants, collects complex information, performs medical assessments, and answers detailed questions with supervision from a medically licensed professional

Benefits

• Employees in this position can expect to receive benefits such as generous vacation, holidays, and sick leave; competitive insurances and savings accounts; retirement benefits.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level