Medix · 20 hours ago
Part - Time Clinical Research Coordinator
Norman, OK, US
Full-time
Onsite
New Grad, Entry LevelMedix is dedicated to providing workforce solutions across multiple industries, and they are seeking a Part-Time Clinical Research Coordinator to join their team. The role involves coordinating clinical trials, managing data collection, and ensuring compliance with regulatory requirements while working up to 20 hours a week.
MedicalPharmaceuticalWholesale
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 be patient facing
Qualification
Required
Strong PART-TIME Clinical Research Coordinator experience
Ability to work 20 hours a week, M-F daytime hours (8-5)
Experience in source documents, data collection, data entry, query resolution, triggering financial payments, study close out and liaison with the sponsor/CRO
Participation in the identification of potential clinical trial participants, screening for eligibility, and enrolling participants per protocol
Coordination of the schedule of events for clinical trial participants from screening to follow up according to protocol
Collection, verification, organization, and recording of clinical information and data in electronic data capture systems (EDC)
Experience in EDC tracking, reviewing validation, updating, SAE reconciliation, lab data reconciliation and safety coding
Working knowledge of essential documents and IRB requirements
Participation in site feasibility determination, site qualification visits, site initiation visits and research related meetings
Experience in recruiting clinical trials to site
May be patient facing
Background check based on job duties, which may include patient care, working with vulnerable populations, access to financial and confidential information, driving, working with heavy machinery, or working in a warehouse or laboratory environment
Company
Medix
At Medix Distribution, we have designed solutions to meet the medical needs for the betterment of society as a whole.
Founded in 2007
11-50 employees
Funding
Current Stage
Early StageCompany data provided by crunchbase