What are the responsibilities and job description for the Clinical Research Coordinator - 77030 position at Medix™?
Hybrid Clinical Research Coordinator
Must Haves: Must have previous experience in Clinical Research and have experience with Oncology Data
Hours: 40 hours per week, between days and times of Monday-Friday 8am-5pm, 1-2 days onsite to assist with data entry/query resolution
Location: Houston, TX
Contract Duration: 6 month contract
Benefits: Medical, Dental, Vision, time off, etc.
Type of Study: Oncology
Role & Responsibilities:
- May be the sole coordinator or work in collaboration with a research nurse on studies, responsible for source documents, data collection, data entry, query resolution, triggering financial payments, study close out and liaison with the sponsor/CRO
- Participates in the identification of potential clinical trial participants, screens them for eligibility, and enrolls participants per protocol
- Coordinates the schedule of events for clinical trial participants from screening to follow up according to protocol
- Collects, verifies, organizes and records clinical information and data in electronic data capture systems (EDC). Abstracts data from necessary sources to complete the EDC and resolve queries.
- Performs the following data related activities: EDC tracking, reviewing validation, updating, SAE reconciliation, lab data reconciliation and safety coding
- May be responsible for regulatory submissions.
- Need working knowledge of essential documents and IRB requirements
- Participates in site feasibility determination, site qualification visits, site initiation visits and research related meetings
- May be responsible for recruiting clinical trials to site
- May have patient contact
Job Description:
- Scheduling/Appointment Reminders, Medical Record Retrieval, Data Entry
Apply Today!
Salary : $20 - $30
