Referral Coordinator

Medix™; Houston (TX); On-site; USD 54,000 - 66,000; Full time

Job summary

Medix is hiring a Clinical Research Referral Coordinator for our Houston, TX site. The role focuses on managing patient referrals, prescreenings, and communications with potential participants to support enrollment goals.

Experience in ophthalmology ( retina preferred ) is highly valued. Responsibilities include maintaining documentation in clinical trial management systems and collaborating with research teams to ensure a smooth referral process.

Qualifications

• College degree or higher is required.
• Ophthalmology experience required; retina experience preferred.
• Strong communication, organizational, and interpersonal skills.
• Familiarity with research protocols and informed consent.

Responsibilities

• Manage patient referrals.
• Conduct prescreenings.
• Communicate with potential participants.
• Support enrollment goals.
• Maintain documentation in clinical trial management systems.
• Collaborate with research teams to ensure a smooth referral process.

Skills

Ophthalmology experience

Referral management

Prescreenings

Clinical trials

Education

College degree or higher

Job description

We're Hiring: Clinical Research Referral Coordinator!

Houston, TX | On-Site

Starting at $60K annually | Monday-Friday, 8 AM-5 PM

Our team is growing, and we're looking for a motivated, detail-oriented professional with ophthalmology experience (retina preferred) to join the team!

In this role, you'll play a key part in clinical trial recruitment by managing patient referrals, conducting prescreenings, communicating with potential participants, and supporting enrollment goals. You'll also maintain accurate documentation in clinical trial management systems and collaborate closely with research teams to ensure a smooth referral process.

What we're looking for:

• College degree or higher
• Ophthalmology experience required; retina experience preferred
• Strong communication, organizational, and interpersonal skills
• Familiarity with research protocols and informed consent

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