Clinical Research Coordinator Jobs in Milwaukee, WI

Summary Perform the day-to-day administrative activities of the clinical research trials program. Provide support to the team to facilitate the achievement of the program’s goals. Primary Responsibilities Recruit, screen, enroll and obtain consent from program participants. Conduct or coordinate training for program participants. Coordinate research protocols including arranging necessary appointments and procedures, working collaboratively with other departments and institutions, and maintaini…

Summary Coordinate the day-to-day administrative activities of the clinical research trials program. Provide support to the team to facilitate the achievement of the program’s goals. Recruit, train, and supervise staff and manage study budgets. Primary Responsibilities Oversee the recruitment, screening, enrolling and obtaining of consent from program participants. Conduct or coordinate training for program participants. Coordinate research protocols including arranging necessary appointments a…

Summary 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 Responsibilities Recruit, screen, enroll and obtain consent from program participants. Conduct or coordinate training for program participants. Coordinate research protocols including arranging necessary appointments and proce…

Summary 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 patient recruiting, training. And supervising staff and managing the program budget. Preferred Schedule Night shift position with predominantly weekday hours. Expected schedule is four nights per week (9:00 PM–7:00 AM), typically Monday–Friday, with occasional weekend coverage as needed for study needs. Flexib…

Summary 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 Responsibilities Recruit, screen, enroll and obtain consent from program participants. Conduct or coordinate training for program participants. Coordinate research protocols including arranging necessary appointments and proce…

Summary Perform the day-to-day administrative activities of clinical research trial programs. Provide support to the Center for Precision Oncology and Rare Cancers team to facilitate the achievement of the program’s goals. Primary Responsibilities Recruit, screen, enroll and obtain consent from program participants. Conduct or coordinate training for program participants. Coordinate research protocols including arranging necessary appointments and procedures, working collaboratively with other …

Summary Coordinate the day-to-day administrative activities of the clinical research trials program. Provide support to the team to facilitate the achievement of the program’s goals. Recruit, train, and supervise staff and manage study budgets. Primary Responsibilities Oversee the recruitment, screening, enrolling and obtaining of consent from program participants. Conduct or coordinate training for program participants. Coordinate research protocols including arranging necessary appointments a…

Summary Coordinate the day-to-day administrative activities of the clinical research trials program. Provide support to the team to facilitate the achievement of the program’s goals. Recruit, train, and supervise staff and manage study budgets. Primary Responsibilities Oversee the recruitment, screening, enrolling and obtaining of consent from program participants. Conduct or coordinate training for program participants. Coordinate research protocols including arranging necessary appointments a…

At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing company currently operates 20 sites across the US and Canada, with plans for further expansion. Join Us in Improving Lives through Clinical Research At Headlands Research, we're not just building a …

The Department of Pediatrics at the Medical College of Wisconsin (MCW) and Children’s Wisconsin (CW) seeks a board certified/board eligible physician to join our Pediatric Emergency Medicine Section. Our successful funding for research, education and quality work has allowed us to expand our section. We are also excited to have moved into a new ED space in October 2023. This position is being recruited at the Assistant Professor or Associate Professor rank. About Pediatric Emergency Medicine We…

Job Description The Froedtert and the Medical College of Wisconsin (F & MCW) Transplant Service Line, and the MCW Division of Gastroenterology & Hepatology are seeking a Board Certified / Board Eligible transplant hepatologist to serve as the medical director and lead our liver transplant hepatology team. This is a leadership position with opportunity to enhance ones own academic career while mentoring and supporting the academic career of others in a vibrant & growing academic transplant cente…

Summary Under general supervision, assist in various administrative and data collection aspects of clinical research studies. Primary Responsibilities Coordinate patient visits to clinic. Organize study participant charts and files, and distribute to appropriate location Collect required data from study coordinators and research nurses, and enter onto clinical research forms and into computerized database Verify accuracy of bills and stipends Generate letters to be sent to study participants Un…

Summary Under general supervision, assist in various administrative and data collection aspects of clinical research studies. Primary Responsibilities Coordinate patient visits to clinic. Organize study participant charts and files, and distribute to appropriate location Collect required data from study coordinators and research nurses, and enter onto clinical research forms and into computerized database Verify accuracy of bills and stipends Generate letters to be sent to study participants Un…

Summary Under general supervision the Clinical Research Quality Assurance Specialist II is responsible for the oversight of clinical research study protocols of increasing complexity, with an emphasis on quality, training, monitoring, and the development of tools for study team use. The Clinical Research Quality Assurance Specialist II will coordinate the day-to-day administrative activities of the program and will provide support to teams to facilitate the achievement of the program’s goals. P…

Summary The Associate Director for Clinical Trial Operations and Workforce Development provides strategic and operational leadership for clinical trial activities within the Clinical and Translational Science Institute (CTSI) at the Medical College of Wisconsin (MCW). This position oversees the CTSI Clinical Trials Office and the Adult Translational Research Unit (A-TRU), ensuring excellence in clinical research operations, compliance, and staff development. The incumbent will build and lead sy…