Clinical Research Coordinator
APEX RESEARCH GROUP LLC
Job Description
Job Description
Benefits:
- Health insurance
- Paid time off
- 401(k)
- Competitive salary
- Dental insurance
- Opportunity for advancement
- Training & development
- Vision insurance
- Coordinate and manage day-to-day clinical trial operations in accordance with study protocols
- Screen, enroll, and follow up with study participants while ensuring informed consent compliance
- Collect, record, and maintain accurate clinical data in electronic data capture (EDC) systems
- Liaise with sponsors, IRBs, and regulatory agencies to ensure study compliance and timely submissions
- Monitor patient safety and report adverse events per GCP and FDA guidelines
- Prepare and maintain regulatory binders, source documents, and study files
- Collaborate with principal investigators and clinical staff to support study milestones and timelines
- Bachelor's degree in life sciences, healthcare, or a related field
- 1-3 years of experience in clinical research coordination or a related clinical setting
- Working knowledge of GCP, ICH guidelines, and FDA regulations
- Experience with EDC systems and clinical trial management software (CTMS)
- SOCRA or ACRP certification (CCRP or CCRC) preferred
- Strong organizational skills with exceptional attention to detail
- Excellent communication and interpersonal skills for working with patients and research teams
Vacancy posted more than 2 months ago
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