**Seeking a Clinical Research Coordinator in Austin, TX**
We are a leading clinical research organization dedicated to advancing ophthalmic science and patient care. Our team is committed to conducting ethical, high-quality studies in strict adherence to ICH-GCP guidelines and IRB-approved protocols.
Position Overview
As the Clinical Research Coordinator, you will be the cornerstone of our clinical trial operations—responsible for coordinating patient visits in alignment with ICH-GCP standards and protocol requirements. You’ll collaborate across teams to ensure compliance, data integrity, and participant safety.
Key Responsibilities
- Coordinate and facilitate daily clinical trial activities according to ICH-GCP and IRB-approved protocols.
- Administer sponsor-required questionnaires (e.g., VFQ).
- Collaborate with supply coordinators to ensure sufficient inventory of kits, shippers, and other essentials.
- Train study staff on protocol procedures, informed consent, and manuals, and ensure documentation of training.
- Create and maintain thorough source documents for each trial.
- Attend teleconferences and Investigator Meetings as directed by the Research Director.
- Review and interpret study protocols, timelines, inclusion/exclusion criteria, and confidentiality/privacy procedures.
- Partner with study and clinical teams to recruit, screen, and document eligibility of study participants.
Minimum Qualifications
Education:
- College degree preferred, but significant relevant experience will also be considered.
- Ophthalmic experience is a plus.
Experience / Skills:
- 1–3 years of relevant clinical research coordination experience, or demonstrated excellence in prior performance evaluations.
- Strong oral and written communication.
- Ability to deliver safe, protocol-compliant care to study participants.
Certifications / Training:
- ICH-GCP Training and Certificate required.
- IATA Certification required.
Why Join Us?
- Collaborate within a driven and mission-focused clinical research team.
- Play a vital role in advancing ophthalmic clinical research in a dynamic, growing city.
- Opportunity for professional growth and impact through high-quality data, compliance, and protocol execution.
