Job Description
Company : Medical Device Mfg. Company.
Position : Medical & Regulatory Writer (On-Site)
Location: Ahmedabad, Gujarat
Experience Required:
Minimum 5+ years strong experience in Clinical Evaluation Reports (CERs) and executing clinical studies for non-active implantable medical devices.
Role Overview:
Medical and Regulatory Writer to lead the clinical and regulatory documentation efforts for non-active implantable medical devices. This role will also be responsible for design and develop clinical protocols and execute clinical studies (pre-market or post-market studies) with minimal supervision. The candidate should have extensive experience in clinical evidence generation strategy and scope research topics to provide recommendations on clinical trial strategy. The ideal candidate will bring in-depth knowledge of international medical device regulations, robust scientific writing capabilities, and demonstrated experience in end-to-end clinical evaluation and evidence ge...
Position : Medical & Regulatory Writer (On-Site)
Location: Ahmedabad, Gujarat
Experience Required:
Minimum 5+ years strong experience in Clinical Evaluation Reports (CERs) and executing clinical studies for non-active implantable medical devices.
Role Overview:
Medical and Regulatory Writer to lead the clinical and regulatory documentation efforts for non-active implantable medical devices. This role will also be responsible for design and develop clinical protocols and execute clinical studies (pre-market or post-market studies) with minimal supervision. The candidate should have extensive experience in clinical evidence generation strategy and scope research topics to provide recommendations on clinical trial strategy. The ideal candidate will bring in-depth knowledge of international medical device regulations, robust scientific writing capabilities, and demonstrated experience in end-to-end clinical evaluation and evidence ge...
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