Description:

Job Summary: Looking to hire an individual with a nursing or clinical research background to act as the Clinical Research Coordinator for a research site in San Diego, CA on an Ophthalmology clinical trial. This position will help identify patients for enrollment through chart review, patient follow-up and pre-screening. This individual will be doing data entry, regulatory, specimen collection, and consenting patients.

Duties and Responsibilities:

• Chart review of patient’s medical records

o EMR- must be proficient in navigating EMR systems

• Patient pre-screening against the criteria for enrollment

• EDC data entry

• Scheduling patient appointments for their in-person study visit

• Regulatory Support

o Specimen Collection

Skills:

EDC, EMR, Ophthalmology, Clinical Research Coordinator

Top Skills Details:

Data Entry, Chart Review, Ophthalmology

Additional Skills & Qualifications:

• Required: Must have experience as a Clinical Research Coordinator and experience working in Ophthalmology

Experience Level:

Entry Level

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.

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At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:

• Hiring diverse talent

• Maintaining an inclusive environment through persistent self-reflection

• Building a culture of care, engagement, and recognition with clear outcomes

• Ensuring growth opportunities for our people

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

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