Clinical Research Coordinator I Dash

Clinical Research Coordinator I Dash

21 Dec 2025
Wisconsin, Milwaukee, 53201 Milwaukee USA

Clinical Research Coordinator I Dash

JOB REQUIREMENTS: Position Description: Clinical Research Coordinator

I - Diagnostic, Anesthesia, and Surgical Health (DASH) Purpose Perform

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 - Abilities

Knowledge 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: Specifications Appropriate experience may be substituted

for education on an equivalent basis Minimum Required Education:

Associate's Degree Minimum Required Experience: 1 year Preferred

Education: Bachelor's Degree Preferred 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 For full info follow application link. EEO/AA

Minorities/Females/Vets/Disability The Medical College of Wisconsin is

an affirmative action/equal opportunity employer and does not

discriminate in hiring or employment on the basis of age, sex, race,

color, religion, national origin, veteran status, disability or sexual

orientation. APPLICATION INSTRUCTIONS: Apply Online:

ipc.us/t/F77858A6C4934E18 Qualified females, minorities, and special

disabled veterans and other veterans are encouraged to apply.

Related jobs

  • JOB REQUIREMENTS: Position Description: Purpose 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 Functions 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. Assist in the preparation of IRB documents and reports. Assist in the evaluation and writing of research protocols. 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 - Abilities 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: Specifications Appropriate experience may be substituted for education on an equivalent basis Minimum Required Education: Associate\'s Degree Minimum Required Experience: 1 yearCertification: 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 For full info follow application link. EEO/AA Minorities/Females/Vets/Disability The Medical College of Wisconsin is an affirmative action/equal opportunity employer and does not discriminate in hiring or employment on the basis of age, sex, race, color, religion, national origin, veteran status, disability or sexual orientation. APPLICATION INSTRUCTIONS: Apply Online: ipc.us/t/FFB29B813E4A425F Qualified females, minorities, and special disabled veterans and other veterans are encouraged to apply.

  • Research Engagement Coordinator

  • Research Analyst – Expert Witness Services

  • Research Analyst – Expert Witness Services

  • Research Analyst – Expert Witness Services

  • Research Analyst – Expert Witness Services

  • Crohn\'s Disease Clinical Study, Payment Up to $2,000

Job Details

Jocancy Online Job Portal by jobSearchi.