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?
Submit Your Resume
Fill out my online form.
