Clinical Research Associate
3 days ago
Job Summary:
Medix™ is seeking a highly skilled and detail-oriented Clinical Research Coordinator to join our team and assist with vaccine trials. The ideal candidate will play a critical role in coordinating and overseeing the daily activities of clinical trials related to vaccines.
Key Responsibilities:
- Patient Recruitment & Enrollment: Identify, screen, and recruit participants for vaccine trials. Obtain informed consent and ensure eligibility criteria are met.
- Study Coordination: Coordinate all aspects of the vaccine trial, including scheduling patient visits, monitoring patient progress, and maintaining study documentation.
- Data Collection & Management: Collect and enter data accurately into clinical databases. Ensure data integrity and adherence to the study protocol.
- Compliance: Ensure compliance with all regulatory requirements, study protocols, and Good Clinical Practice (GCP) guidelines. Assist with the preparation of regulatory submissions as needed.
- Communication: Serve as a point of contact between the research team, participants, and external stakeholders. Communicate effectively with physicians, nurses, and other healthcare professionals involved in the trial.
- Safety Monitoring: Monitor and report adverse events, ensuring participant safety throughout the study.
- Documentation: Maintain accurate and complete records of study activities, including patient files, study logs, and regulatory documents.
- Training & Support: Provide training and support to staff involved in the vaccine trial. Assist in preparing for audits and inspections.
Additional Details:
- Hours: Monday-Friday; Onsite 5 Days a Week; Normal Business Hours
- Employment/Duration: ~13 Month Contract
- Pay: $30/hr-$45/hr (dependent on background and years of experience)
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