Clinical Research Specialist II
2 weeks ago
Clinical Research Coordinator II - Medix™
Schedule: Monday - Friday, 8am-5pm
Compensation: $45.00 per hour
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 therapies. This position entails managing studies related to various health conditions, including asthma, Chronic Obstructive Pulmonary Disease (COPD), and Macular Degeneration. If you are dedicated to advancing clinical research and improving patient outcomes, we encourage you to consider this opportunity.
Key Responsibilities:
- Oversee the complete lifecycle of clinical trials, ensuring smooth operations from initiation to conclusion.
- Collaborate with sponsors, CROs, and regulatory agencies to uphold protocol and compliance standards.
- Engage in the recruitment, screening, and informed consent processes for study participants.
- Organize and conduct participant visits, maintaining strict adherence to study protocols.
- Accurately gather and document study data to ensure reliability.
- Preserve data integrity through systematic audits and monitoring activities.
- Adhere to Good Clinical Practice (GCP) guidelines and ethical considerations.
- Serve as the main point of contact for sponsors, CROs, and clinical teams.
- Deliver regular updates and reports on study progress, including any significant events.
Qualifications:
- Bachelor's degree in a relevant scientific field.
- A minimum of 3 years of experience as a Clinical Research Coordinator, with comprehensive knowledge of the entire study process.
- Experience with regulatory compliance and data management is preferred.
- Bilingual proficiency in Spanish and English.
- Experience in phlebotomy is advantageous.
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