What are the responsibilities and job description for the Clinical Research Associate position at Zuswork?
Hours : Full-time / Part-time
Summary :
The Clinical Research Associate (CRA) in Ophthalmology plays a vital role in coordinating and monitoring clinical research studies, ensuring compliance with regulatory requirements and ethical standards.
The CRA works closely with the inter-professional health care and research teams to facilitate the coordination of clinical trials across various sites.
The CRA ensures that ophthalmology clinical studies adhere to Good Clinical Practice (GCP) guidelines, research protocols, and organizational policies.
The CRA is responsible for data collection, monitoring patient safety, and ensuring that all study-related activities are conducted according to protocol.
The CRA demonstrates professionalism, teamwork, attention to detail, and a commitment to high-quality research.
The CRA’s role impacts the organization’s research mission, patient outcomes, and advancements in ophthalmology.
Responsibilities :
Oversee and monitor ophthalmology clinical trials from initiation to completion.
Ensure adherence to study protocols, ethical guidelines, and regulatory requirements (FDA, ICH-GCP, IRB, etc.).
Conduct site visits, including pre-study, initiation, routine monitoring, and close-out visits.
Verify informed consent documentation and ensure participant safety measures are followed.
Collect, review, and verify clinical data accuracy and completeness.
Maintain communication with investigators, sponsors, and research teams to facilitate smooth study execution.
Identify and resolve issues related to protocol deviations, compliance, and data quality.
Ensure accurate and timely reporting of adverse events and protocol deviations.
Assist in training site personnel on study procedures and compliance requirements.
Ensure proper documentation and record-keeping for regulatory audits and inspections.
Collaborate with internal and external teams, including ophthalmologists, study coordinators, and regulatory bodies.
Perform other duties as assigned to support clinical research operations.
Requirements
Credentials :
Certification in clinical research (e.g., ACRP, SOCRA) preferred.
CPR certification from the American Heart Association preferred.
Education or Equivalent Experience :
Bachelor’s degree in life sciences, healthcare, or a related field required.
Master’s degree preferred.
Prior experience in clinical research or ophthalmology studies is highly desirable.
We believe that the best research outcomes start with the best support for our employees. Our employee benefits programs help our team members maintain a healthy work-life balance. We offer a comprehensive compensation and benefits program, which includes tuition assistance, career development, and growth opportunities. Our employees are actively engaged in groundbreaking ophthalmology research, contributing to medical advancements that improve patient outcomes.
Benefits
Excellent training program is offered
Employee pay is determined by multiple factors, including geography, experience, qualifications, skills and local minimum wage requirements
In addition, you may also be offered a competitive bonus and / or commission plan, which complements a first-class total rewards package
Benefits may include health care, retirement savings, paid time off / vacation, and various employee discounts
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