Medix™ · 1 week ago
Clinical Research Specialist - 249661
Medix™ is seeking a Clinical Research Specialist to support the Project Manager in coordinating day-to-day operations. The role involves assisting with study protocol implementation, developing project materials, and ensuring regulatory compliance.
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Responsibilities
Ensure all study activities are executed in strict compliance with established protocols and regulatory requirements (IRB, institutional certifications)
Securely access Electronic Health Records (EHR), update online tracking software, and manage diverse datasets with high accuracy
Coordinate stakeholder meetings, maintain meticulous meeting minutes, and organize complex documentation
Act as a real-time liaison between the study team, Principal Investigators, and project managers; escalate any protocol deviations or issues immediately
Monitor enrollment numbers and assist in the logistics of launching new studies (expected launch within 3–4 weeks for the third study)
Qualification
Required
Must have a foundational understanding of the research environment (preferably in academia/public health)
Proficiency in Microsoft Office Suite (specifically Outlook and Word) and the ability to navigate Microsoft Teams
Ability to complete institutional certifications and protocol-specific training within a two-week ramp-up period
Must be flexible depending on projects to move shifts to 7:30am-4:30pm or 9am-6pm
Preferred
Education: Graduates of MPH (Master of Public Health), Epidemiology, or Statistics programs
Clinical Research Coordination Experience
Company
Medix™
Medix provides workforce solutions to clients and creates opportunity for contract employees.
Funding
Current Stage
Late StageTotal Funding
unknown2022-09-16Acquired
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