Central Study Coordinator
Central Study Coordinator
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Job Description
Job Title: Central Study Coordinator
Job Location: Raleigh NC USA
Job Location Type: Remote
Job Contract Type: Fulltime
Job Seniority Level: Entry level
The Central Study Coordinator position is responsible for clinical monitoring for assigned protocols and investigational sites as well as ensuring that studies are conducted and documented in accordance with the study protocol standard operating procedures Good Clinical Practices (GCP) and other applicable regulatory requirements.
Minimum Requirements
- Research experience preferred
- Ability to manage technology and webbased research platforms on PC (Microsoft OS) laptop in the remote workspace
- Study Team experience is ideal
- Critical thinking skills
- Strong communication Skills (verbal and written)
- Ability to work independently and collaboratively with RAs/CSCs to complete delegated tasks as needed
- Working location that has the ability to maintain privacy
***ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please no phone calls or emails to anyone regarding this posting.***
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Employment Type
Full Time
