Clinical Research Coordinator II - Psychiatry

Primary Functions

• 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.
• Maintain oversight of 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.
• Maintain oversight of 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.
• Collaborate with the principal investigator to manage study resources.
• Organize internal and external meetings, site visits, and special events specific to the study.
• Aid in recruitment, training and scheduling of study team volunteer staff.
• Collaborate 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.

Qualifications

• Appropriate experience may be substituted for education on an equivalent basis.
• Minimum Required Education: Bachelor’s Degree.
• Minimum Required Experience: 2 years.
• Preferred Education: Master of Science, Master of Public Health, Master of Arts.
• Preferred Experience: 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.