A Clinical Writer is needed for a 12-month contract position at major device company in Mid-West.
The Clinical Writer partners with Subject Matter Experts, Medical Directors and clinical team to create clinical study related documents in accordance with ICH, regulatory authority, and/or company’s guidelines. Creates a variety of clinical documents necessary for all phases ...
:: If you meet the qualifications listed below and would like more information contact Dave at 815-756-1221. Attach resume when responding to this posting ::
The Regulatory Specialist will be responsible for providing subject matter expertise to assure regulatory and safety compliance through discipline use and thorough knowledge of regulatory requirements and procedures.
The Regulatory Affairs Specialist works with a team of Regulatory Affairs professionals to ensure completion of Product Controllership and UDI deliverables in the area of product remediation and new product development.
Key responsibilities/essential functions include:
Create Registration program records for US registered products in IRIS
Create US country records for each registration ...
May 30 -
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