Clinical Research Coordinator II
4 weeks ago
We are seeking a highly skilled Clinical Research Coordinator II to join our team at MCW: SARGEANT HEALTH CENTER. The successful candidate will be responsible for performing day-to-day administrative activities of clinical research trial programs, providing support to the team to facilitate the achievement of the program's goals, and assisting with recruiting, training, and supervising staff and managing the program budget.
Key Responsibilities:
* Recruit, screen, enroll, and obtain consent from program participants.
* Conduct or coordinate education and training for program participants.
* Project/patient coordination for research protocols, including arranging necessary appointments and procedures, working collaboratively with other departments and institutions, and maintaining contact with study participants.
* Monitor study-related activities on patient and protocol level, maintaining patient calendars, screening, and enrollment information utilizing software tools.
* Collect, analyze, and disseminate research data, reporting clinical trial progress to study investigators.
* Work with the Principle Investigator to develop, implement, and maintain comprehensive databases and files related to the program.
* Identify problems or obstacles in the system/procedures related to the implementation of the research protocols and communicate to the study investigators.
* Maintain program timeline, including tracking deadlines for program components.
* Ensure compliance with all relevant IRB and other regulatory agency requirements.
* Prepare IRB documents and reports.
* Evaluate and assist with writing of research protocols in collaboration with the study investigator.
* Participate in partner-related committees.
* Collaborate on the development of program materials, including educational materials, marketing materials, websites, forms, and reports.
* Coordinate program outreach activities, including acting as a liaison with community organizations.
* 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.
Requirements:
* Bachelor's degree
* Minimum 2 years of clinical research coordination experience
* Science education; biology, biochemistry, immunology, etc.
* CITI training within 90 days of hire
* Certified Clinical Research Professional (ACRP or SoCRA)
MCW: SARGEANT HEALTH CENTER 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.
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