Clinical Evidence Specialist

Job Summary

A company is looking for a Global Clinical Evidence Specialist.

Key Responsibilities

• Support the development and creation of Clinical, Scientific, and Regulatory documents in accordance with global requirements
• Conduct literature reviews, synthesize scientific evidence, and develop clinical evidence reports
• Collaborate with cross-functional teams to develop, review, and finalize Clinical Evaluation Reports and related documentation

Required Qualifications

• Bachelor's degree (B.S./B.A.) or equivalent combination of education and relevant industry experience
• Minimum of 5 years of clinical trial experience within the medical device industry or a related regulated industry
• Strong computer proficiency, including Microsoft Office and Adobe
• Working knowledge of global regulatory guidelines and requirements, including U.S. FDA regulations and ISO standards
• Demonstrated ability to prioritize and manage multiple tasks effectively