Clinical Scientist

Clinical Scientist

Anywhere

Type: Permanent

Category: Clinical Ops

Industry: Life Sciences

Workplace Type: Remote

Reference ID: JN -112025-104407

Date Posted: 01/11/2026

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Description:

Remote

Our client is a PE-backed medical device organization advancing next-generation technologies in atrial fibrillation and cardiac ablation. As the team prepares for two global Class III IDE studies, the Clinical Development and Science function is expanding to support protocol development, safety oversight, and scientific leadership. The role provides exposure to electrophysiology and Pulse Field Ablation, contributing to the scientific, clinical, and strategic elements of cardiac ablation innovation.

This is a full-time, permanent opportunity, offering a competitive salary and comprehensive benefits package. Qualified applicants must be willing and able to work on a w2 basis.

Salary: $130,000 - $150,000/ yr. w2

Responsibilities:

Responsibilities

• Lead development of clinical study protocols, case report forms, and associated study documents.

• Support clinical safety oversight, including adverse event review, vigilance, and coordination with the Clinical Events Committee.

• Contribute scientific input into study design, endpoints, and overall clinical strategy.

• Review and interpret clinical data to support study reports, publications, and regulatory submissions.

• Collaborate closely with Clinical Operations, Field Clinical, Regulatory, and Quality teams.

• Participate in discussions with key opinion leaders, investigator meetings, and internal scientific reviews.

• Ensure scientific consistency across programs and alignment with regulatory and clinical goals.

• Support the development of data collection tools and ensure clarity, accuracy, and completeness.

• Assist with medical writing elements related to clinical reports and study documentation.

Experience Requirements:

Experience Requirements

• Electrophysiology and Pulse Field Ablation experience required.

• Background supporting clinical studies in industry or academia.

• Strong understanding of clinical research methods and safety reporting.

• Ability to evaluate and interpret clinical data.

• Strong scientific writing skills and attention to detail.

• Ability to collaborate effectively across Clinical Development, Operations, and Regulatory functions.

• Excellent communication and analytical capabilities.

• Prior experience as a Clinical Scientist in medical devices preferred.

• Experience with Class III devices or IDE studies preferred.

• Experience contributing to regulatory submissions or interacting with health authorities preferred.

• Experience working with electrophysiologists, key opinion leaders, or clinical event committees preferred.

Education Requirements:

Education Requirements

• MS, PhD, or MD.

Recruitment Transparency Notice

Eliassen Group values transparency in our recruitment practices. Please be advised that Eliassen Group utilizes artificial intelligence (AI) tools as part of its initial application screening process. You may receive email and SMS notifications from the Eliassen Virtual Recruiting Team ( [email protected] , 781-808-2924) inviting you to complete a brief voice screening as part of your application process. These tools assist our hiring teams in different ways, including but not limited to, assistance in reviewing application materials to help identify candidates whose qualifications most closely match the requirements of the position. All AI-assisted evaluations and responses are reviewed by human recruiters before any hiring decisions are made. The use of AI in our process is intended to support fairness, efficiency, and consistency, and Eliassen Group takes measures to prevent bias or discrimination in connection with its hiring practices. By proceeding, you acknowledge, agree, and consent to Eliassen Group's use of these tools, including AI tools, as part of the application and hiring process.

Skills, experience, and other compensable factors will be considered when determining pay rate. The pay range provided in this posting reflects a W2 hourly rate; other employment options may be available that may result in pay outside of the provided range.

W2 employees of Eliassen Group who are regularly scheduled to work 30 or more hours per week are eligible for the following benefits: medical (choice of 3 plans), dental, vision, pre-tax accounts, other voluntary benefits including life and disability insurance, 401(k) with match, and sick time if required by law in the worked-in state/locality.

Please be advised- If anyone reaches out to you about an open position connected with Eliassen Group, please confirm that they have an Eliassen.com email address and never provide personal or financial information to anyone who is not clearly associated with Eliassen Group. If you have any indication of fraudulent activity, please contact [email protected] _.

About Eliassen Group:

Eliassen Group is a leading strategic consulting company for human-powered solutions. For over 30 years, Eliassen has helped thousands of companies reach further and achieve more with their technology solutions, financial, risk & compliance, and advisory solutions, and clinical solutions. With offices from coast to coast and throughout Europe, Eliassen provides a local community presence, balanced with international reach. Eliassen Group strives to positively impact the lives of their employees, clients, consultants, and the communities in which they operate.

Eliassen Group is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, pregnancy, sexual orientation, gender identity, national origin, age, protected veteran status, or disability status.

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