Clinical Research Assistant at Central Florida Eye Specialists

, Florida, United States -

Full Time

Start Date

Immediate

Expiry Date

24 Feb, 26

Salary

0.0

Posted On

26 Nov, 25

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Healthcare, Ophthalmology, Analytical Mindset, Attention to Detail, Interpersonal Skills, Verbal Communication, Written Communication, Laboratory Procedures, MS Office, Data Collection, Clinical Trials, Patient Coordination, Good Clinical Practice, Research Protocols, Compliance, Standard Operating Procedures

Industry

Medical Practices

Description

Company Overview Love what you see, see what you love! Our mission is to enhance the quality of life for each patient by providing compassionate and excellent care using the latest advancements in healthcare. We offer a full spectrum of medical and surgical treatments so that all options are available to our patients. Central Florida Eye Specialists takes pride in practicing our core values: Quality, Respect, Compassion, and Excellence. Our amazing leadership team is committed to cultivating and maintaining an employee centric work environment where every employee has a voice and a platform to share their ideas and suggestions, are encouraged and incentivized to broaden their education and training and are invited to participate in the numerous employee activities offered monthly. Central Florida Eye Specialists is affiliated with EyeSouth Partners' premier network of Ophthalmic Medical Services. Position Summary We are now hiring for a Clinical Research Assistant that will support a high-volume Research Department within an ophthalmic practice that focuses on providing quality and compassionate care to each patient needing complete eye care services. Responsibilities A CRA is responsible for performing procedures and coordinating the execution of clinical trials in accordance with research protocols. • Recruit and screen subjects to participate in trials• Coordinate patient visits and perform procedures related to research• Collect accurate data obtained from research visits• Monitor research participants to ensure adherence to study protocol• Adhere to Good Clinical Practice (GCP) guidelines including regulatory and ethical standards• Maintain relationships with site staff, study subjects, and sponsor delegates• Perform other related duties as assigned by the Clinical Research Coordinator• Maintain compliance with all research Standard Operating Procedures (SOPs) Qualifications Education and/or Work Experience Requirements: • 2+ years in healthcare, preferably ophthalmology, but not necessarily in clinical research• Analytical mindset• Attention to detail• Exceptional interpersonal skills• Superior verbal and written communication skills• Understanding of laboratory procedures and equipment• Proficiency in MS Office – Word, Excel and Outlook• High school diploma or equivalent GED Company Benefits We offer a competitive benefits package to our employees: Medical Dental Vision 401k w/ Match HSA/FSA Telemedicine Generous PTO Package We also offer the following benefits for FREE: Employee Discounts and Perks Employee Assistance Program Group Life/AD&D Short Term Disability Insurance Long Term Disability Insurance EyeSouth Partners is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. #IND

Responsibilities

The Clinical Research Assistant is responsible for performing procedures and coordinating the execution of clinical trials in accordance with research protocols. This includes recruiting and screening subjects, coordinating patient visits, collecting data, and ensuring adherence to study protocols.