Clinical Research Coordinator II

Position Description:

Purpose

Perform the day-to-day administrative activities of clinical research trial programs. Provide support to the team to facilitate the achievement of the program's goals. Assist with recruiting, training, and supervising staff and managing the program budget.

Primary Functions

* Recruit, screen, enroll and obtain consent from program participants GOOD Study randomized control trial, data registry, and biobank. Conduct or coordinate training for program participants.

* Coordinate research protocols including arranging necessary appointments and procedures, working collaboratively with other departments and institutions, and maintaining contact with study participants.

* Collect, analyze, and disseminate research data. Report program data and progress to study investigators and program stakeholders including DSMB, GOOD Study Steering and Subspecialty Committees, division/department/organizational leadership, external sponsors, regulatory bodies, and collaborators. Work with Principal Investigator to develop, implement, and maintain comprehensive databases and files related to the program.

* Identify problems or obstacles in the system/procedures related to implementation of the research protocols and communicate to the study investigators.

* Assure compliance with all relevant IRB and other regulatory agency requirements.

* Prepare IRB documents and reports to the NIH. Evaluate and write of research protocols in collaboration with the study investigator.

* Collaborate on the development of program materials including educational materials, marketing materials, websites, forms, and reports. Maintain and update GOOD Study Clinicaltrials.gov page(s). Assist in maintenance of GOOD Study webpage, as needed.

* Maintain program timeline including tracking deadlines for program components.

* Coordinate program outreach activities including acting as a liaison for the 38 participating sites. Organize internal and external meetings, site visits, and special events.

* Monitor study related budgets. Participate in the development of program resources through literature searches, contact with outside programs, and review of funding opportunities.

Preferred Schedule:

Position Requirements:

Specifications

Appropriate experience may be substituted on equivalent basis

Minimum Required Education: Bachelor's degree

Minimum Required Experience: 2 years

Preferred Education: Bachelor's or equivalent

Certification: CITI training within 90 days of hire

MCW as an Equal Opportunity Employer and Commitment to Non-Discrimination


The Medical College of Wisconsin (MCW) is an Equal Opportunity Employer. We are committed to fostering a diverse community of outstanding faculty, staff, and students, as well as ensuring equal educational opportunity, employment, and access to services, programs, and activities, without regard to an individual's race, color, national origin, religion, age, disability, sex, gender identity/expression, sexual orientation, marital status, pregnancy, predisposing genetic characteristic, or military status. Employees, students, applicants or other members of the MCW community (including but not limited to vendors, visitors, and guests) may not be subjected to harassment that is prohibited by law or treated adversely or retaliated against based upon a protected characteristic.

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