Clinical Research Assistant

Responsibilities

• Perform procedures and coordinate the execution of clinical trials in accordance with research protocols.
• Recruit and screen subjects to participate in trials.
• Cookordinate patient visits and perform procedures related to research.
• Collect accurate data obtained from research visits.
• Maintain relationships with site staff, study subjects, and sponsor delegates.
• Monitor research participants to ensure adherence to study protocol.
• Adhere to Good Clinical Practice (GCP) guidelines including regulatory and ethical standards.
• Perform other related duties as assigned by the Clinical Research Coordinator.

Requirements

• 2+ years in healthcare, preferably ophthalmology, but not necessarily in clinical research.
• An analytical mindset.
• An attention to detail.
• Exceptional interpersonal skills.
• Superior verbal and written communication skills.
• A understanding of laboratory procedures and equipment.
• A proficiency in MS Office - Word, Excel and Outlook.
• A high school diploma or equivalent.

Qualifications

• A high school diploma or equivalent.

Skills

• Understanding of laboratory procedures and equipment.
• Proficiency in MS Office - Word, Excel and Outlook.

Benefits

We offer a competitive benefits package to our employees including:

• Medical
• Dental
• Vision
• 401(k) with Match
• HSA/FSA
• Telereimedicine
• 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

For more information related to our benefits offered, please follow the link to our benefits page here.

EyeSouth Partners is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.