Are you interested in working in clinical research? Do you have a background in nursing or life sciences and are interested in bringing innovation to your community? Do you want to use your strong organizational skills to help others? If so, a position as a clinical research coordinator might be the fit for you. Clinical Research Coordinators conducting studies in a private, ophthalmology practice is a position that allows ongoing growth and development. As an clinical research coordinator, you’ll assist principal investigators in recruiting and management research studies directly affecting the eyecare industry. Join Visionary Eye Institute to grow in this exciting position and start your new career!

Visionary Eye Institute was founded by Dr. Ehsan Sadri in 2019 to advocate for all communities by providing innovative and life-changing eyecare. Our practice specializes in medical eyecare and surgery, and we also have a clinical research division that allows us to offer the highest-level care to Los Angeles and Orange County. We have excellent benefits including paid holiday, and medical/dental benefits. Come join our caring and professional team today!

EDUCATION AND EXPERIENCE:

1. Bachelor’s degree in nursing or life sciences.

2. 3+ years’ work experience for a pharmaceutical company or related field

3. Experience as an ophthalmic technician preferred but not required.

ESSENTIAL SKILLS AND ABILITIES:

1. Proficient understanding of marketing and statistics.

2. Outstanding communication skills, both verbal and written.

3. Proficient with Microsoft Office Word and Excel.

4. Ability to work independently and prioritize duties.

5. Understanding of electronic data capture.

6. Strong organization with attention to detail.

7. Analytical problem-solving skills.

8. Demonstrated ability to meet deadlines.

KEY RESPONSIBILITIES:

1. Develops and outlines trial protocols.

2. Develops and maintains site certification for ongoing studies.

3. Trains clinical research staff on protocol requirements, proper source documentation, and case report form completion.

4. Works with the physicians on ethics regarding rights, safety, and well-being of trial subjects.

5. Develops protocols to protect subjects’ confidentiality.

6. Manages all trial materials.