Radiant Research (radiantresearch.com) is comprised of 20 wholly-owned premier clinical research centers nationwide. Our clinical research centers provides a critical service to biopharmaceutical companies by recruiting study participants into clinical research, conducting the clinical research protocol and collecting the data necessary to support the safety and efficacy of the drug company's product to the FDA. Our client list includes every major pharmaceutical company and contract research ...
• Signaling on drug and device safety data
• Preparation of epidemiology sections of risk management plans
• Preparation of aggregate safety information for risk analysis reports
• 1-3 years experience in an industry or University environment.
• Excellent oral and written communication skills.
• Excellent capabilities in Excel, Word, PowerPoint
• Ability to program in SAS a plus.
NO sponsorship, NO relocation. US based candidates only, please
Ensure execution of a clinical study program (IIIB/IV studies supporting marketed products) within timeline and on budget, utilizing internal resources or overseeing CRO activities
Write full or sections of protocol based on approved synopsis
Develop quality supporting documents, e.g., manual of operations, informed consent
Ensure Health Authority and IRB submission and approval
Participate in site selection and evaluation process
Interact with clinical supply ...
Jan 24 -
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