Regulatory Writing jobs

• 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.

• United States of America
• US$140000 - US$190000 per annum
• Posted 15 days ago

Job Title: Senior Medical Writer OR Associate Director, Medical Writing (Regulatory) Location: Hybrid schedule in San Francisco, New Jersey, or New York Position Overview: A bio-pharmaceutical company is seeking a highly skilled and experienced Senior Medical Writer or Associate Director, Medical...

• 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...

• Tuttlingen
• Negotiable
• Posted 24 days ago

We have a current opportunity for a QA/RA Manager on a permanent basis. The position will be based in Tuttlingen. For further information about this position please apply. You can look forward to these tasks: * Evaluation, selection and continuous monitoring of suppliers in accordance with intern...

• 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...