Ophthalmic Clinical Research Coordinator

Randstad USA; Dallas (TX); On-site; USD 52,000 - 58,000; Full time

Benefits offered by this job

Medical insurance

401K plan

Dental & Vision

Job summary

Randstad USA in Dallas seeks a Clinical Research Coordinator for Texas' largest retina practice. You will support ophthalmic trials, ensure protocol adherence, and collaborate with elite specialists in a fast-paced clinical environment.

Location is Dallas, TX with a permanent, full-time role. Salary ranges from $52,000 to $58,000 with a 9 to 5 schedule and a comprehensive benefits package. Education begins at a High School diploma or GED.

Qualifications

• Minimum 1 year of Clinical Research Assistant or Coordinator experience in an Ophthalmic practice.
• High school diploma or GED equivalent.
• Proven training in medical terminology and strong knowledge of OSHA, HIPAA, and GCP standards.
• Demonstrated ability to perform patient triage and respond appropriately to urgent clinical situations.

Responsibilities

• Manage clinical trial data collection, process queries, and ensure timely protocol resolution.
• Identify and report adverse events while maintaining compliance with FDA and GCP guidelines.
• Conduct pre-study, initiation, monitoring, and close-out visits with sponsor representatives.
• Perform patient intake, administer topical/oral ophthalmic medications, and counsel patients on physician orders.
• Maintain regulatory documentation including IRB approvals, protocol amendments, and safety reports.

Skills

Site Initiation

Patient Scheduling

Visit Coordination

Education

High School diploma or GED

Tools

NextGen

Patient Management software

Job description

job summary:

Join Texas' largest, most experienced retina practice in Dallas, TX, as a Clinical Research Coordinator! Work alongside elite specialists running cutting-edge clinical trials in a fast-paced, highly collaborative clinical environment.

location: Dallas, Texas

job type: Permanent

salary: $52,000 - 58,000 per year

work hours: 9 to 5

education: High School

responsibilities:

• Manage clinical trial data collection, process queries, and ensure timely protocol resolution.
• Identify and report adverse events while maintaining compliance with FDA and GCP guidelines.
• Conduct pre-study, initiation, monitoring, and close-out visits with sponsor representatives.
• Perform patient intake, administer topical/oral ophthalmic medications, and counsel patients on physician orders.
• Maintain regulatory documentation including IRB approvals, protocol amendments, and safety reports.

qualifications:

Required:

• Minimum 1 year of Clinical Research Assistant or Coordinator experience in an Ophthalmic practice.
• High school diploma or GED equivalent.
• Proven training in medical terminology and strong knowledge of OSHA, HIPAA, and GCP standards.
• Demonstrated ability to perform patient triage and respond appropriately to urgent clinical situations.

Preferred:

• Specific experience in a Retinal practice.
• Hands-on proficiency with NextGen and Patient Management software.

skills:

Site Initiation, Patient Scheduling and Visit Coordination

Equal Opportunity Employer:

Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.

At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact [e-mail].

Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility).

This posting is open for thirty (30) days.