Demo

Clinical Mapping Specialist

Precision Life Sciences
Burlington, MA Full Time
POSTED ON 1/12/2025
AVAILABLE BEFORE 2/21/2025

We are looking for a Clinical Mapping Specialist to be a key member of our high functioning Data Science team, leading important clinical and preclinical data acquisition and interpretation activities. This person will gain system-level understanding of a novel and potentially game-changing technology in a fast-moving field and grow their career in design and R&D.

Responsibilities

  • Support complex clinical and preclinical studies in the US and EU, including setting up and operating the mapping system, providing technical and clinical guidance during the procedure, documenting results, and supporting post-procedure data analysis to drive future system development.
  • Work closely with leading EP physicians to gain voice-of-customer feedback and drive design requirements.
  • Support the systems engineering team in translating user and clinical needs into technical requirements.
  • Develop training materials.
  • Work with R&D teams to define clinical workflows.
  • Review case data and support publications.
  • Train clinicians and EP lab staff on system usage and study protocols.
  • Extensive travel required.
Skills and Experience
  • Minimum of a BA/BS required, MS in Biomedical Engineering or similar desired.
  • 5 years working with commercially available high-resolution mapping systems.
  • Significant experience with the entire EP ecosystem, including RF generator, EP recording system, pacing and diagnostic catheters, and electrogram interpretation. PFA experience preferred.
  • Experience with complex software tools and spatiotemporal computations on electrograms.
  • Supported 300 EP procedures with various workflows including anatomical, signal- based, and map-guided ablation.
  • Deep understanding of EP and cardiac arrhythmias.
  • Ability to develop and maintain relationships with key EP opinion leaders.
  • Excellent verbal and writing skills.
  • Comfortable working in both a fast-paced and rigorous early-stage startup environment with fluid requirements, as well as a regulated later-stage process-driven setting.
  • Experience working in a regulated environment with Design Control and compliant QMS systems.

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