Note: The job is a remote job and is open to candidates in USA. The Medical College of Wisconsin is looking for an experienced, full-time Clinical Research Coordinator II for the National Institutes of Health-funded SOLO Study which is a clinical trial of screening interventions to increase detection of anal cancer. The individual will coordinate research activities at multiple sites, ensuring compliance with protocols and managing study resources.
Responsibilities
- Prepare documents to assure compliance with Institutional Review Board and other regulatory agency requirements
- Ensure successful creation and disbursement of recruitment material and advertisements for trial participants. Recruit, screen, consent and enroll program participants
- Recruit Community Advisory Board members and maintain board
- Conduct the activities of the study clinics
- Collect both quantitative and qualitative research data. Report study-related data and progress to management, study investigators and sponsor as required
- Support participants with appointments and maintain contact with participants to meet protocol-driven timelines. Monitor the study related activities on a participant and protocol level
- Identify problems or obstacles in the system/procedures related to implementation of the research protocols and communicate to the study investigators and study team
- Support participants with appointments and maintain contact with participants to meet protocol-driven timelines. Monitor the study related activities on a participant and protocol level
- Work with team members to develop, implement and maintain comprehensive research databases
- Oversee the development of study materials including websites, forms, and reports
- Work with study biostatistician, data analyst, and data manager to prepare study data for publication
- Work with the principal investigator on creation of manuscripts for the peer-reviewed literature
- Work closely with principal investigator to manage study resources
- Organize internal and external meetings, site visits, and special events specific to the study
- Assist in recruitment, training and scheduling of study team volunteer staff
- Work collaboratively with other institutions and medical clinics
- Evaluate and write research protocols in collaboration with the study investigator
- Participate in writing and responding to funding opportunities
Skills
- Bachelor's Degree
- 2 years of experience
- CITI training within 90 days of hire
- Certified Clinical Research Professional preferred and required within 6 months of employment
- Knowledge of clinical trial design, documentation, and records management
- Excellent oral and written communication skills
- Strong critical thinking, problem solving and attentiveness to detail
- Strong computer skills
- Knowledge of clinical research study principles including appreciation for protocol adherence and human subject research ethics
- Competency with communities at increased risk for HIV infection
- Master of Science, Master of Public Health, Master of Arts
- 5 years of experience in research program coordination
- Experience with program management in a medical research or educational environment preferred
- Prior work with clinical research preferred
Benefits
- Outstanding Healthcare Coverage, including but not limited to Health, Vision, and Dental. Along with Flexible Spending options
- 403B Retirement Package
- Competitive Vacation and Paid Holidays offered
- Tuition Reimbursement
- Paid Parental Leave
- Employee & Family Assistance Program (EFAP)
- Pet Insurance
- On campus Fitness Facility, offering onsite classes
- Additional discounted rates on items such as: Select cell phone plans, local fitness facilities, Milwaukee recreation and entertainment etc.
Company Overview
Company H1B Sponsorship