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Senior Clinical Trial Coordinator
2 months ago
Clinical Research Coordinator II - Medix™
Schedule: Monday - Friday, 8am-5pm
Compensation: $45.00 per hour
Location: Not specified
Position Overview:
Medix™ is seeking a committed Clinical Research Coordinator II to enhance our research initiatives, working closely with sponsors and Contract Research Organizations (CROs) to facilitate clinical trials for innovative treatments. This position is pivotal in managing studies related to various health conditions, including respiratory diseases and ocular disorders. If you are driven by the pursuit of clinical excellence and wish to contribute to patient well-being, we encourage you to consider this opportunity.
Key Responsibilities:
- Oversee the complete lifecycle of clinical trials, ensuring efficient operations from initiation to conclusion.
- Collaborate with sponsors, CROs, and regulatory agencies to uphold protocol and compliance standards.
- Engage in the recruitment and screening of participants, ensuring informed consent is obtained.
- Organize and conduct participant visits, maintaining strict adherence to study protocols.
- Accurately gather and document study data to support research objectives.
- Uphold data integrity through systematic audits and monitoring processes.
- Ensure adherence to Good Clinical Practice (GCP) and ethical guidelines throughout the research process.
- Serve as the primary liaison for sponsors, CROs, and clinical teams, facilitating effective communication.
- Provide comprehensive updates and reports on study progress, including documentation of any adverse events.
Qualifications:
- Bachelor's degree in a relevant scientific field.
- A minimum of 3 years of experience as a Clinical Research Coordinator, with proficiency in all phases of clinical trials.
- Experience with regulatory compliance and data management is preferred.
- Bilingual proficiency in Spanish and English is advantageous.
- Experience in phlebotomy is a plus.
