Clinical Scientist

Clinical Scientist

Anywhere

Type:
Permanent

Category:
Clinical Ops

Industry: Life Sciences

Workplace Type:
Remote

Reference  -

Date Posted: 01/11/2026

Shortcut:

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.

(Full‑time, Permanent) Competitive salary and comprehensive benefits package. Qualified applicants must be willing and able to work on a W2 basis.

Salary: $130,000 - $150,000/year W2

• 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.

• 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.

• MS, PhD, or MD.

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.