Senior Clinical Trials Associate
3 weeks ago
Join Our Team:
As a Clinical Research Coordinator at California Retina Consultants, you will be responsible for the day-to-day management of clinical trials, working closely with our experienced team to ensure high-quality research outcomes.
Primary Responsibilities:
- Oversee research patient visits, aligning with ICH-GCP guidelines and IRB-approved study protocols.
- Coordinate daily clinical trial activities, fostering collaboration among team members to optimize study efficiency.
- Establish and maintain accurate source documents, encompassing study protocols, timelines, inclusion/exclusion criteria, and confidentiality/privacy protections.
- Manage study supplies, facilitate staff training, and oversee data collection, entry, and reporting.
- Screen participants, collect medical history, adverse events, and serious adverse events, and ensure timely reporting to sponsors and IRBs.
- Engage in informed consent discussions, address participant inquiries, and implement amended consent forms.
- Provide secondary review oversight during informed consent and collect data according to protocol requirements.
Remuneration Package:
Our compensation package includes a salary range of $55,000 - $75,000 annually, based on experience, along with additional benefits and opportunities for professional development.
About California Retina Consultants:
We are a renowned ophthalmology practice dedicated to delivering exceptional patient care and advancing the field of retinal research through innovative clinical trials.
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