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Clinical Research Coordinator - 233382
Medix™ • Oak Park, IL 60303 • Posted 3 days ago via LinkedIn
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In-person • Full-time • $30.00-$45.00/hr • Contract • Mid Level
Job Highlights
Using AI ⚡ to summarize the original job post
We are seeking a dedicated 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, including patient recruitment, data collection, and ensuring compliance with study protocols and regulatory requirements. This is a 13-month contract role based in Oak Park, IL.
Responsibilities
- Identify, screen, and recruit participants for vaccine trials.
- Obtain informed consent and ensure eligibility criteria are met.
- Coordinate all aspects of the vaccine trial, including scheduling patient visits, monitoring patient progress, and maintaining study documentation.
- Collect and enter data accurately into clinical databases.
- Ensure compliance with all regulatory requirements, study protocols, and Good Clinical Practice (GCP) guidelines.
- Serve as a point of contact between the research team, participants, and external stakeholders.
- Monitor and report adverse events, ensuring participant safety throughout the study.
- Maintain accurate and complete records of study activities, including patient files, study logs, and regulatory documents.
- Provide training and support to staff involved in the vaccine trial.
- Assist in preparing for audits and inspections.
Full Job Description
13 Month Contract Clinical Research Coordinator role in Oak Park, IL (60302)
Position Summary:
We are seeking a dedicated 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. This includes patient recruitment, data collection, and ensuring compliance with study protocols and regulatory requirements.
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:
- Location: Oak Park, IL (60302)
- Hours: Monday-Friday; Onsite 5 Days a Week; Normal Business Hours
- Employment/Duration: ~13 Month Contract
- Pay (Dependent on background and years of experience): $30/hr-$45/hr
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