Clinical Research Coordinator

A Clinical Research Coordinator helps facilitate the coordination of pharmaceutical-sponsored clinical trials within varied therapeutic areas. The ideal candidate will be experienced in clinical trials, specifically in ICH-GCP and Phase II-IV studies, should be able to complete tasks efficiently and independently, and should be able to communicate and collaborate with research and office staff, as well as research monitors and sponsors.

Responsibilities:

• Complete and ensure the quality of case report forms
• Conducting study visits, including vital signs, ECG, laboratory specimen handling and shipment
• Dispense medication and record in source documents
• Ensure the confidentiality of study information and protect patient privacy
• Maintain and track medication inventory
• Maintain documentation regarding all aspects of the studies
• Participate in investigator meetings
• Perform patient screenings and enrollment for clinical studies
• Prepare for monitoring visits, work closely with monitors
• Preparing and maintaining clinical trial source documents

Job Requirements:

• 1+ years of experience as a clinical research coordinator or clinical research assistant
• 4-year degree preferred; will consider applicant with research experience in lieu of 4-year degree
• Ability to complete assignments and meet deadlines
• Capable to coordinate multiple tasks/projects and meet deadlines in a fast paced environment
• Ability to work independently as well as collaboratively in a team environment
• Attention to detail
• Proficiency with electronic medical records (EMR) and clinical trial management systems
• Self-directed, proactive and timely in the management of assignments

What Do You Want To Do Next?

1. Speak with someone about my staffing needs
2. Learn about full-time recruiting services
3. Submit my resume to staffing company