Medical College of Wisconsin
Clinical Research Coordinator I - DASH Pediatrics
Medical College of Wisconsin, Milwaukee, Wisconsin, United States, 53244
Position Description:
Clinical Research Coordinator I - Diagnostic, Anesthesia, and Surgical Health (DASH)PurposePerform the day-to-day administrative activities of the pediatric DASH clinical research program. Provide support to the team to facilitate the achievement of the program's goals.Primary Functions
Assist in the preparation of IRB documents and reports. Assist in the evaluation and writing of research protocols.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 maintaining contact with study participants.Collect, analyze, and disseminate program data. Report program data and progress to program stakeholders.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.Collaborate on the development of program materials including educational materials, marketing materials, websites, forms, and reports.Work with Principal Investigator to develop, implement, and maintain comprehensive databases and files related to the program.Maintain program timeline including tracking deadlines for program components.Coordinate program outreach activities including acting as a liaison with community organizations.Knowledge - Skills - AbilitiesKnowledge of clinical research functions and regulations.Knowledge of biology, chemistry, mathematics, documentation, and records management.Data utilization, complex problem solving, critical thinking, resource management, and writing skills.
Preferred Schedule:
Position Requirements:
SpecificationsAppropriate experience may be substituted for education on an equivalent basisMinimum Required Education: Associate's DegreeMinimum Required Experience: 1 yearPreferred Education: Bachelor's DegreePreferred Experience: Experience working in clinical research and familiarity with research protocols and regulations.Certification: CITI training within 90 days of hire
#LI-NI1
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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Clinical Research Coordinator I - Diagnostic, Anesthesia, and Surgical Health (DASH)PurposePerform the day-to-day administrative activities of the pediatric DASH clinical research program. Provide support to the team to facilitate the achievement of the program's goals.Primary Functions
Assist in the preparation of IRB documents and reports. Assist in the evaluation and writing of research protocols.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 maintaining contact with study participants.Collect, analyze, and disseminate program data. Report program data and progress to program stakeholders.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.Collaborate on the development of program materials including educational materials, marketing materials, websites, forms, and reports.Work with Principal Investigator to develop, implement, and maintain comprehensive databases and files related to the program.Maintain program timeline including tracking deadlines for program components.Coordinate program outreach activities including acting as a liaison with community organizations.Knowledge - Skills - AbilitiesKnowledge of clinical research functions and regulations.Knowledge of biology, chemistry, mathematics, documentation, and records management.Data utilization, complex problem solving, critical thinking, resource management, and writing skills.
Preferred Schedule:
Position Requirements:
SpecificationsAppropriate experience may be substituted for education on an equivalent basisMinimum Required Education: Associate's DegreeMinimum Required Experience: 1 yearPreferred Education: Bachelor's DegreePreferred Experience: Experience working in clinical research and familiarity with research protocols and regulations.Certification: CITI training within 90 days of hire
#LI-NI1
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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