Clinical Research Coordinator

Description

River Region Psychiatry Associates is seeking a Clinical Research Coordinator (CRC) to conduct clinical research studies in depression, anxiety, and trauma. The CRC will work independently on progressively more complex projects/assignments, independently manage significant and key aspects of a large study or all aspects of one or more research studies. We are seeking an experienced research professional with a proven track record of conducting clinical research. Working knowledge of psychiatric conditions is preferred, but it is more important that applicants have a strong research background and solid experience with the systems necessary for the implementation of complex protocols. 

JOB DUTIES & RESPONSIBILITIES 

Recruitment and Enrollment: Oversee participant recruitment, determine strategies for promoting and retaining participants, and meet enrollment goals. 

Data Management: Develop systems for data collection, reporting, and analysis. 

Project Management: Develop project schedules and targets, lead team meetings, and prepare minutes. 

Supervision and Training: Train and mentor new staff or students, possibly including hiring and performance evaluations. 

Compliance and Auditing: Ensure compliance with regulations, audit operations, and monitor Institutional Review Board submissions. 

Collaboration and Reporting: Collaborate with principal investigators and sponsors, monitor adverse events, and resolve queries. 

Policy Improvement: Recommend and implement improvements to policies and processes. 

Budget Management: Develop study budgets, track milestones, and invoice sponsors. 

Regulatory Compliance: Ensure compliance with regulatory bodies, manage document inspections, and handle FDA and IRB submissions. 

Requirements

Education 

• Required: Bachelor’s degree in a related field and two years of clinical research experience, or equivalent education and experience 
• Preferred certification from the Society of Clinical Research Associates or Association of Clinical Research Professionals. 

Experience 

• 3–5 years in clinical research, experience with industry sponsors is a plus. 

Skills 

• Strong knowledge of research rules, interpersonal skills, proficiency in Microsoft Office and databases, understanding of medical terminology, and experience with regulatory bodies (HIPAA, FDA, IRB, GCP).