Job Description

Job Position:

We are seeking a Clinical Research professional to support our team in conducting high-quality research studies while ensuring patient safety and compliance with study protocols.

Key Responsibilities:

• Schedule subject visits per protocol guidelines
• Prepare visit-specific documentation and charts for the Clinical Research Coordinator
• Assist in monitoring subject flow and subject care
• Observe, assist, collect, and record data for follow-up visits
• Administer required questionnaires to study participants
• Conduct electrocardiograms (ECGs) per study protocols
• Request and manage medical records for Serious Adverse Event reporting
• Process and ship laboratory biological samples
• Obtain written re-consents from study participants when necessary
• Complete sponsor-required training and certifications
• Perform other duties as assigned

Minimum Qualifications:

Education:

• High School diploma or equivalent with relevant experience (Required)
• College degree (Preferred)
• Ophthalmic experience (Preferred)

Experience/Skills:

• Previous human subjects research (Required)
• Strong oral and written communication skills
• Ability to deliver safe and appropriate patient care in accordance with study protocols
• Detail-oriented with excellent organizational skills

Details:

Location: Wake Forest, NC

Pay Rate: (Dependent on experience)

Hours: Monday - Friday; Normal Business Hours; Onsite 5 Days a Week

Duration: Direct Hire

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