Medical Writer Specialist

CooperCompanies • Trumbull, CT

4d

About The Position

The Medical Writer is responsible for developing, writing, and managing
high-quality clinical and regulatory documents that support compliance and
product lifecycle needs for global standards such as EU MDR and FDA regulations.
 This includes planning, implementing, and reporting clinical data collection
for Post-Market Clinical Follow-up (PMCF) and clinical trials, ensuring
adherence to global regulatory standards. The role stays current with scientific
literature and regulatory requirements.

Responsibilities

• Developing, writing, and managing high-quality clinical and regulatory documents
• Planning, implementing, and reporting clinical data collection for Post-Market Clinical Follow-up (PMCF) and clinical trials
• Ensuring adherence to global regulatory standards
• Staying current with scientific literature and regulatory requirements

What This Job Offers

• Job Type: Full-time
• Education Level: No Education Listed
• Number of Employees: 501-1,000 employees