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Medical Director
1 month ago
We are seeking a highly skilled and experienced Principal Investigator to join our team at Eximia Research. As a Principal Investigator, you will be responsible for the execution, planning, and management of assigned studies, ensuring the highest level of quality and compliance with regulatory requirements.
Key Responsibilities:- Provide medical direction and review of protocols to ensure compliance with investigational plans and good clinical practice.
- Provide medical expertise and scientific feasibility for new sponsor inquiries.
- Ensure the safety and well-being of all participants in the study.
- Ensure data collected at the study site is credible and accurate.
- Ensure the rights, integrity, and confidentiality of all participants in the trial are protected.
- Assist and provide guidance to clinical operations, research staff, and sponsor client managers as required.
- Obtain and/or review participants' medical history.
- Perform physical assessments, examinations, and study procedures as required by study protocols.
- Evaluate and interpret clinical data and diagnostic information.
- Immediately report Serious Adverse Events (SAEs) to sponsors and the IRB as required.
- Oversee the administration of Investigational Product.
- Review and adhere to study protocol.
- Maintain proper documentation.
- Ensure accuracy, completeness, legibility, and timeliness of data reported and be consistent with source documents.
- Minimum qualifications include an M.D or D.O with an active medical license.
- Must have experience in one of the following specialties: Internal Medicine, Primary Care, Emergency Medicine, Neurology, Gastroenterology, or Endocrinology.
- Board certification or board eligibility in a specialty appropriate to the type of research being conducted at the site.
- Medical licensure (license must be valid in the state in which the research is conducted).
Eximia Research is a fully integrated research sites network of premier investigational sites meeting the clinical research needs of global biopharmaceutical, biotechnology, medical device, pharmaceutical, and clinical research organizations (CROs). Our premier, multidisciplinary wholly owned research sites located across the country are known for excellent trial execution, rapid subject recruitment/enrollment, and delivery of quality data.