Fda Researcher Jobs in Arkansas (NOW HIRING)

Oak Ridge Institute for Science and Education is offering a research opportunity with the FDA's Center for Drug Evaluation and Research. The role involves developing methods for identifying adverse ...

In executing these position responsibilities, the Research Assistant is guided FDA regulations, Good Clinical Practice (GCP), and company standard operating procedures and policies. Responsibilities:

In executing these position responsibilities, the Research Assistant is guided FDA regulations, Good Clinical Practice (GCP), and company standard operating procedures and policies. Responsibilities:

The primary function of a Clinical Research Nurse II (CRN) is to coordinate clinical research ... FDA, indirectly supervises data management with any aspect of protocol initiation coordination and ...

Preferred Qualifications FDA/HHS/NIH/CDC/NASA experience. PMP, PE, CFM, or equivalent. Research campus experience.

Preferred Qualifications • FDA/HHS/NIH/CDC/NASA experience. • PMP, PE, CFM, or equivalent. • Research campus experience.

Preferred Qualifications · FDA/HHS/NIH/CDC/NASA experience. · PMP, PE, CFM, or equivalent. · Research campus experience.

In executing these position responsibilities, the Clinical Research Coordinator is guided by FDA regulations, Good Clinical Practice (GCP), and company standard operating procedures and policies.

The Research Quality and Regulatory Specialist will support the department by ensuring adherence to ... Prepare, track, and maintain all correspondence and documentation required by the IRB, FDA, and ...

Ensure alignment with federal regulations (45 CFR 46, FDA, USDA, PHS, 42 CFR 93, etc.). * Review research protocols, amendments, renewals, and disclosures. * Conduct audits, inspections, and ...

Prepares for and participates in FDA inspections. * Communicates effectively with IRBs, sponsors, investigators, and research team members. KPA 2 - Patient Recruitment, Screening & Enrollment ...

Prepares for and participates in FDA inspections. * Communicates effectively with IRBs, sponsors, investigators, and research team members. KPA 2 - Patient Recruitment, Screening & Enrollment ...

Performs all study-start-up activities - initial IRB Submission, initial FDA Form 1572, initial ... Notifies Clinical Research Coordinator of consent form and protocol changes when necessary.

Previous experience in clinical research. * Knowledge of FDA regulations, HIPAA, and ICH-GCP guidelines. * Experience with digital marketing, social media advertising, or community outreach.

... GCP), FDA regulations, and sponsor requirements. Job Duties / Responsibilities: * Provide ... Improve research department & management efficiency. * Manage departmental staffing, workload ...

In addition to initial FDA submissions, the Research Regulatory Specialist must understand pertinent regulations, manage adverse event reporting, handle annual reports, coordinate communication with ...

Evolution Research Group (ERG) is dedicated to delivering high-quality Phase I-IV clinical trial ... Sign the Form FDA 1572 as appropriate. * Sign the protocol as required. * Sign sponsor contract(s ...

The Research Regulations Specialist II is responsible for preparing research submissions to the IRB ... sponsor, FDA, healthcare providers and IRB. * Manage special projects as assigned such as ...

At least 1-2 years of EEG experience; prior work in clinical research setting strongly preferred. * Knowledge of ICH-GCP and FDA regulations is an asset. * Proficiency in EEG interpretation software ...

... FDA, USDA, and international labeling regulations. * Collaborate with FSQA to ensure labels meet all food safety and regulatory requirements. * Work with R&D to accurately reflect product ...