Regulatory Writing jobs
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- Nottingham
- Negotiable
- Posted 2 days ago
We have a current opportunity for a Regulatory / Medical Writer on a contract basis for up to 40 hours per week. The position will be fully remote, dedicated to a renowned CRO. Experience within oncology is desired. Further information about this position please apply.
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- Cork
- Negotiable
- Posted 15 days ago
Role: Clinical Evaluation Specialist Consultant Tasks: Writing Clinical Evaluation Plans Writing Clinical Evaluation Reports Post market Clinical Follow Up Plans & Reports All focusing around EU Medical Device Regulation with a specific focus on Implantable Bio-materials. Start date: ASAP Contrac...
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- United States of America
- Negotiable
- Posted about 1 month ago
Job Overview The Clinical Evaluation Reporting Specialist is tasked with creating Clinical Evaluation Reports (CERs) for Terumo Blood and Cell Technologies (TBCT) products. This involves utilizing product labeling, preclinical and clinical data, published literature, risk management documents, co...