Clinical Team Supervisor

The Clinical Team Supervisor will function on the Management Team of an oncology 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 and/or Data 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.

Work location(s) may include: Highland Avenue and the East Park Medical Center

• 15% Schedules logistics and secures resources for a defined clinical research trial of high complexity and/or multiple research trials
• 25% Recruits, screens, and enrolls trial participants, collects complex information, performs medical assessments, and answers detailed questions with supervision from a medically licensed professional
• 15% Collects, prepares, processes, analyzes, and submits participant data and samples to appropriate entities, adhering to research protocols and compliance with applicable policies and procedures
• 10% Assists with review of current research trials, development of operational protocols and work unit policies, and makes recommendations to leadership for improvements
• 20% Serves as a subject matter expert and main point of contact for clinical research participants providing information regarding research procedures, expectations, and informational inquiries
• 15% 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

Diversity is a source of strength, creativity, and innovation for UW-Madison. We value the contributions of each person and respect the profound ways their identity, culture, background, experience, status, abilities, and opinion enrich the university community. We commit ourselves to the pursuit of excellence in teaching, research, outreach, and diversity as inextricably linked goals.

The University of Wisconsin-Madison fulfills its public mission by creating a welcoming and inclusive community for people from every background - people who as students, faculty, and staff serve Wisconsin and the world.

For more information on diversity and inclusion on campus, please visit: Diversity and Inclusion

Preferred
Bachelor's Degree
Preferred focus: Nursing, biomedical, social science, or related field.

-Minimum 2 years of experience coordinating oncology clinical trials
-Nursing degree preferred but not required.

SOCRA- Certification in Clinical Research Required, Clinical Research Certification required to be obtained within 6 months of hire
CCRP, ACRP, CCRA, CCRC, ACRP-CP all comparable certifications

Required

SOCRA- Certification in Clinical Research Preferred
CCRP, ACRP, CCRA, CCRC, ACRP-CP all comparable certifications

Full Time: 100%

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.

Ongoing/Renewable

Minimum $70,000 ANNUAL (12 months)
Depending on Qualifications
The starting salary for the position is $70,000 but is negotiable based on experience and qualifications.

University sponsorship is not available for this position, including transfers of sponsorship. The selected applicant will be responsible for ensuring their continuous eligibility to work in the United States (i.e. a citizen or national of the United States, a lawful permanent resident, a foreign national authorized to work in the United States without the need of an employer sponsorship) on or before the effective date of appointment. This position is an ongoing position that will require continuous work eligibility.

-TB testing and a Caregiver Background check will be required at the time of employment. 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.

There is one vacancy available for this posting, within our Early Phase Disease-Oriented Team (DOT). The position will supervise Clinical Research Coordinators on the Early Phase team.

To apply for this position, please click on the "Apply Now" button. To apply for this position, please click on the "Apply Now" button. You will be asked to upload a current resume/CV and a cover letter briefly describing your qualifications and experience.

Jennifer Wilkie
jwilkie@wisc.edu
608-262-8025
Relay Access (WTRS): 7-1-1. See RELAY_SERVICE for further information.

Clinical Research Supervisor(RE019)

A53-MEDICAL SCHOOL/CARBONE CANC CTR/CANC CTR

Academic Staff-Renewable

312217-AS