
Research Trials Specialist
2 weeks ago
We are seeking a skilled and detail-oriented Clinical Research Coordinator to support our clinical trials. The ideal candidate will have experience in managing clinical trials, ensuring regulatory compliance, and maintaining accurate records.
This role involves coordinating with Principal Investigators, understanding study protocols, and communicating protocol issues to relevant stakeholders. Additionally, the successful candidate will be responsible for collecting patient information, conducting vital signs, and maintaining accurate records of study medication.
Key Responsibilities:- Manage clinical trials from initiation to completion, ensuring adherence to federal regulations and company guidelines.
- Communicate effectively with Principal Investigators, Site Administrators, and other stakeholders to resolve protocol issues.
- Maintain accurate and timely source documentation and sponsor-required information.
In addition to these responsibilities, the Clinical Research Coordinator will educate patients and family members regarding their particular study and provide general information about clinical drug trials.
Requirements:- Bachelor's degree in a related field preferred; HS diploma or GED required.
- Minimum 2 years of experience in a clinical environment; experience in clinical research ideal.
- LPN, RN, or other medical licensure or certification.
- Strong working knowledge of GCP and FDA guidelines.
- Knowledge of medical terminology.
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