Clinical Research Regulatory Specialist overseeing clinical trials in ophthalmology with focus on participant care and regulatory compliance. Ensuring safety and communication with various stakeholders in clinical research.
Responsibilities
Comprehends knowledge of scientific concepts related to the design and analysis of clinical trials;
Ensures care of the participants, aspects of human subject protections and safety in the conduct of a clinical research study.
Encompasses study management and GCP compliance; safety management (adverse event reporting) and handling of investigational product.
Facilitates all elements of communication within the site and between the site and sponsor, CRO and regulators; understands teamwork skills critical to responsible conduct of clinical research.
Embraces the principles and practice of leadership and professionalism in clinical research.
Performs other duties as assigned.
Requirements
Bachelor's Degree and some related experience (Required) or Associate's Degree with 4 years of clinical and/or research experience (Required)
Ability to prioritize the work of multiple projects. (Required proficiency)
Detail-oriented person with the ability to work independently on multiple tasks and manage time effectively. (Required proficiency)
Write and edit technical documents. (Required proficiency)
Ability to understand and communicate regulatory requirements to others. (Required proficiency)
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