Clinical Research Coordinator

Benefits

Qualifications

• •Bachelor’s degree in nursing or life sciences
• •3+ years’ work experience for a pharmaceutical company or related field
• •Proficient understanding of marketing and statistics
• •Outstanding communication skills, both verbal and written
• •Proficient with Microsoft Office Word and Excel
• •Ability to work independently and prioritize duties
• •Understanding of electronic data capture
• •Strong organization with attention to detail
• •Analytical problem-solving skills
• •Demonstrated ability to meet deadlines
• •7 more items(s)

Responsibilities

• •Clinical Research Coordinators conducting studies in a private, ophthalmology practice is a position that allows ongoing growth and development
• •As an clinical research coordinator, you’ll assist principal investigators in recruiting and management research studies directly affecting the eyecare industry
• •Develops and outlines trial protocols
• •Develops and maintains site certification for ongoing studies
• •Trains clinical research staff on protocol requirements, proper source documentation, and case report form completion
• •Works with the physicians on ethics regarding rights, safety, and well-being of trial subjects
• •Develops protocols to protect subjects’ confidentiality
• •Manages all trial materials
• •5 more items(s)