Clinical Evidence Specialist

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