Clinical Research Coordinator
Ora
Summary
The Clinical Research Coordinator is a full-time, on-site role based at ARENSIA's clinic in Phoenix, AZ. This role is responsible for coordinating and executing day-to-day clinical trial activities, including participant screening, enrollment, scheduling, and visit management.
Job description
The Clinical Research Coordinator ensures adherence to study protocols, manages informed consent processes, and maintains accurate source documentation and regulatory files. Daily tasks include data collection and entry, monitoring participant safety, supporting study assessments and procedures, and collaborating closely with investigators, nurses, and other site staff.
The role also involves communication with sponsors and CROs, assisting with monitoring visits and audits, and contributing to continuous improvement of site processes and patient experience.
Requirements
- Demonstrated clinical research experience, including hands-on involvement in clinical trials and study operations.
- Strong understanding of informed consent procedures and patient rights, with the ability to clearly explain study information to participants.
- Knowledge of study protocols and research methodologies, with the ability to implement protocol requirements accurately in daily practice.
- Experience working within clinical trial frameworks, including compliance with GCP, ICH guidelines, and applicable regulatory standards.
- Relevant education in health sciences, nursing, biology, or a related field; certification in clinical research (e.g., CCRC) is an advantage.
- Excellent organizational skills, attention to detail, and ability to manage multiple studies or tasks simultaneously.
- Strong written and verbal communication skills, with the ability to interact professionally with participants, investigators, and sponsor representatives.
- Comfort working in a fast-paced, early-phase research environment and collaborating as part of a multidisciplinary team on-site in Phoenix, AZ.
Company overview
Ora is the world's leading full-service ophthalmic drug and device development firm, operating as a specialized contract research organization (CRO) focused exclusively on ophthalmology. Founded in 1974 and headquartered in Andover, Massachusetts, the company has over 45 years of experience in advancing eye care innovations globally. Ora provides comprehensive research and development services spanning preclinical studies, clinical trials, regulatory strategy, and product development for both pharmaceutical and medical device companies. With operations across the United States, United Kingdom, Australia, and Asia, the company has helped clients achieve more than 85 product approvals to date. Ora's expertise covers a wide range of ophthalmic conditions including allergy, dry eye, retina diseases, glaucoma, and anti-infective therapies. The company employs over 500 ophthalmology specialists who utilize proprietary clinical models, integrated data solutions, and global regulatory strategies to accelerate product development from concept to market. Ora serves a diverse client base ranging from startups to global pharmaceutical and device companies, positioning itself as the trusted partner for ophthalmic innovation worldwide.