Position Description:
Summary
Perform the day-to-day administrative activities of the neurosciences 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 research participants. Conduct or coordinate training for research participants and study staff.
- Coordinate research protocols including arranging necessary appointments and procedures, working collaboratively with other departments and institutions, and maintaining contact with study participants.
- Collect data from research participants, both in person and via phone. Data collection duties may include performing clinical assessments (e.g. assessments of symptoms, neurological functioning). Data entry into electronic database.
- Assist with biospecimen collection and processing.
- Work in a fast-paced, muti-disciplinary clinical environment with clinical staff in a collaborative fashion. Act as a liaison for research participants and clinical staff.
- Share on-call time and duties with other research staff. Will be required to carry a pager during call, outside of business hours, and respond to hospital within one hour when acute enrollments and study procedures are needed.
- Identify problems or obstacles in the system/procedures related to implementation of the research protocols and communicate to the study team.
- Assure compliance with all relevant IRB and other regulatory agency requirements.
- Assist in the preparation of IRB documents and reports.
- 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.
- Other duties as assigned.
Knowledge - Skills - Abilities
- Knowledge of research, biology, chemistry, mathematics, documentation, and records management.
- Data utilization, complex problem solving, critical thinking, resource management, and writing skills.
- Oral and written communication skills and interpersonal skills are essential.
- Ability to work independent and as part of a team.
Preferred Schedule:
Position Requirements:
Appropriate experience may be substituted for education on an equivalent basis
Minimum Required Education: Associate's Degree
Minimum Required Experience: 1 year
Required Certification/Licensure(s): CITI training within 90 days of hire
Physical Requirements
Work requires occasionally lifting moderate weight materials, standing, or walking continuously.
Work Environment
Occasional exposure to dust, noise, temperature changes, or contact with water or other liquids. Work is performed in an environmentally controlled environment.
Sensory Acuity
Ability to detect and translate speech or other communication required. May occasionally require the ability to distinguish colors and perceive relative distances between objects.
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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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