QI
Clinical Research Coordinator
Quadrant, Inc.
- 🇺🇸 United States
- On-site
- 16 hours ago
- GCP
16 hours ago
Not enough detail in this posting to match
Washington DC McLean, VA
Pay From: $36 Per hour
MUST:
1 plus years of experience in the clinical research field
Experience with data collection
Experience with patient enrollment and screening
Experience evaluating data
Experience working with investigators
Experience preparing for audits and FDA inspections
Ability to coordinate all phases of clinical research trials
Experience entering and updating information in Clinical Trial
Working knowledge of GCP
Experience preparing budgets for studies
DUTIES:
Clinical Research Coordinator will be responsible for, but not limited to the following:
Oversee, prepare, submit and maintain regulatory submissions
Handle the coordination of clinical research activities of all phases and all levels as well as investigator-initiated research
Attend investigator meetings
Enter data into clinical trial system
Monitor and report adverse events
Oversee the informed consent process and review consent forms with research participant
Quadrant is an affirmative action/equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, status as a protected veteran, or status as an individual with a disability.“Healthcare benefits are offered to all eligible employees according to compliance mandated by the Affordable Care Act“.
Clinical Research Coordinator · Quadrant, Inc.