Dedicated clinical research site is looking for the motivated Research Coordinator
Honesty, dedication Integrity, strong work ethics is extremely important.
Excellent computer skills, ability to edit, enter medical data in various electronic systems.
Sound understanding of ICH/ GCP guidelines, HIPPA and clinical research regulations
Informed consent process, recruitment of research study participants.
Blood sample collection, processing, shipping
Study Lab kits, study drug inventory management
Understand blinded/ unblinded component of clinical trials
Update and maintain regulatory binders
Medical science knowledge and ability to extract medical data from electronic medical record as per the research study requirement.
Site Initiation activity. Attend investigator meetings
Ability to interact with monitors, resolve EDC queries, submit AE/ SAE etc
Coordinates and administers research study associated activities. Assists in project planning, and ensures that pre-established work scope, study protocol, and regulatory requirements are followed. Recruits and coordinates research subjects, as appropriate, and serves as principle administrative liaison for the project. Oversees and coordinates the provision of administrative and staff services to director the investigators; develops and maintains recordkeeping systems and procedures.
TRANSFERABLE COMPETENCY REQUIREMENTS: 1. Humbleness. 2. Quickness in understanding the study protocols. 3 Multitasker. 4 Team player. 5. Verbal communications skills 6. Problem-solving skills 7. Planning/organizational skills 8. Personal motivation 9. Project Management capabilities 10. Customer service skills.
This is a rewarding opportunity in stable growing organization.'
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Work Remotely
Job Type: Full-time
Benefits:
- 401(k)
- Dental insurance
- Health insurance
- Paid time off
- Vision insurance
Schedule:
Education:
- High school or equivalent (Preferred)
License/Certification:
- BLS Certification (Preferred)
- Certified Medical Assistant (Preferred)
Work Location: Multiple locations
