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Job Title: Sr. Regulatory Medical Writer
W-2
Location: Home-based
Assignment Duration: 6 month extendable
Write clinical documents for submission to regulatory authorities, including but not limited to: briefing documents, clinical development plans, previous human experience summaries, human pharmacology summaries, investigator brochures, study protocols, model informed consents, interim and final clinical study reports, common technical document (CTD) clinical overviews ...
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 ...
We are looking for a Pharmaceutical Associate Scientist that has protein formulation and process development for at least a 9 month assignment (possible duration up to 2 years) with a major pharmaceutical company in a north suburb of Chicago, IL. Qualified Scientists, outside of the area, are encouraged to apply; however this contract assignment does not offer relocation assistance.
The Associate Protein Scientist will be responsible for
• executing stability studies and characterization ...
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 ...
As a key scientific leader create early clinical research strategies to drive the development of novel oncology therapeutics. Work with our clinics and laboratories to develop novel biomarkers, research tools and study designs derived from the safety, pharmacokinetic and pharmacodynamic data obtain in the early phase trials.
Will:
*** Determine the most efficient study designs, patient population and biomarkers to ensure the success of early clinical research
*** Conceptualize and implement ...
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