A remote role at Clarioclinical.
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Original listing text, shown exactly as published by the company.
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Represent Clario by providing cardiology expertise to pharmaceutical sponsors across consulting services, including protocol design and development, cardiac safety and efficacy strategies, statistical analysis plans, expert report writing, and regulatory representation
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Serve as a cardiology liaison across internal departments, supporting cardiologist activities, cardiac solutions, safety consulting, and cardiac‑related compliance strategies
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Support clinical consulting for Digital Physiology and other Clario endpoints, enabling cross‑business‑unit opportunities and therapeutic area strategies
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Participate in client discussions for prospective and ongoing studies requiring cardiac safety or efficacy approaches
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Assist Cardiac Solutions Scientific and Medical Affairs leadership in developing, maintaining, and updating policies, procedures, and SOPs, including Cardiology Review Guidelines and expanded digital physiology endpoints
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Stay current on scientific advancements in cardiac safety and efficacy and educate internal stakeholders as appropriate
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Support generation of endpoint data through interpretation of ECGs, Holters, patch devices, stress tests, blood pressure variability assessments, and related endpoints, including QA and QC activities
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Contribute to ECG core lab procedures to enhance interpretation quality, consistency, and operational efficiency
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Provide sales support by contributing scientific and clinical expertise as needed
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Support system development and validation efforts for EXPERT and other Clario platforms
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Participate in meetings and research collaborations with regulatory authorities
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Provide leadership in statistical innovation and research, supporting sponsor interactions involving statistical design and analysis and contributing strategically across Clario lines of business.
What We Look For
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MD degree required
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ABIM Board Certification
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Board certification in Cardiovascular Diseases required for U.S.‑based candidates
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Minimum of three years’ experience in the pharmaceutical industry as an employed cardiologist or consultant, particularly in early‑phase development
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Experience authoring reports for QT waivers and working knowledge of clinical pharmacology desirable
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Prior experience working with or consulting for pharmaceutical sponsors
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Demonstrated high ethical standards and commitment to representing Clario with integrity and professionalism.
Clario, a part of Thermo Fisher Scientific, is a leading provider of endpoint technology solutions for clinical trials, transforming lives by accelerating the development of therapies for patients worldwide.
EEO Statement
Clario is an equal opportunity employer. Clario evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status, or any other legally protected characteristic.
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