Clinical Research Coordinator II
4 days ago
Clinical Research Coordinator II
The Clinical Research Coordinator II will be responsible for ensuring the successful execution of clinical trials at assigned investigative sites. This role will involve ensuring compliance with sponsor protocols, FDA regulations, and ICH/GCP guidelines, as well as providing high-quality data to sponsors.
Key Responsibilities:
- Study Execution: Conduct study subject visits, complete protocol-required procedures, and document these in a timely manner.
- Documentation and Data Management: Adhere to ALCOA-C standards, complete data entry, and resolve queries in a timely manner.
- Communication and Collaboration: Liaise with laboratory teams, data teams, administrative staff, clinical investigators, research participants, and sponsor/CRO representatives.
- Administrative Tasks: Submit required administrative paperwork, participate in subject recruitment and retention efforts, and engage with research participants.
Requirements:
- Education: High School Diploma or equivalent required; Bachelor's degree a plus; Foreign Medical Graduates preferred.
- Experience: At least one year of experience as a CRC, preferably with practice coordinating industry-sponsored vaccines in a private setting; At least two years of experience as a research assistant, data coordinator, laboratory personnel, or equivalent experience in a clinical research setting.
- Credentials: ACRP or equivalent certification preferred; Registered Medical Assistant certification or equivalent preferred.
Preferred Qualifications:
- Language Skills: Bilingual in Spanish preferred.
- Skills: Energetic, goal-driven, detail-oriented, and able to multi-task.
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