Therapy Development Manager - Carotid - Shockwave Medical

Johnson & Johnson UK

Chicago, Illinois, United States
Base: $131,000.00 - $210,450.00; bonus/equity: not...
Fully remote
Clinical expert in carotid artery disease
Physician & hospital staff training
Procedural case support
The Therapy Development Manager (TDM) is responsible for being a clinical expert in the treatment of carotid artery disease to support clinical trial excellence, gain treatment insights, and function as a subject matter expert across the organization

Job Summary

  • The Therapy Development Manager (TDM) is responsible for being a clinical expert in the treatment of carotid artery disease to support clinical trial excellence, gain treatment insights, and function as a subject matter expert across the organization.
  • This role will require strong clinical acumen to be successful, including physician and hospital staff training with procedural case coverage to ensure the safe and effective use of IVL.
  • Employees are eligible to participate in the Company’s consolidated retirement plan (pension) and savings plan (401(k)), and are eligible for various time off benefits including vacation, sick time, and holiday pay.

Matching Summary

The Therapy Development Manager (TDM) is responsible for being a clinical expert in the treatment of carotid artery disease to support clinical trial excellence, gain treatment insights, and function as a subject matter expert across the organization.

Salary

Base: $131,000.00 - $210,450.00; Bonus/Equity: Not specified; Benefits: Eligible for Company's consolidated retirement plan (pension) and savings plan (401(k)), long-term incentive program, vacation, sick time, holiday pay, Work/Personal/Family Time, Parental Leave, Bereavement Leave, Caregiver Leave, Volunteer Leave, Military Spouse Time-Off

Skills & Requirements

Must-have

  • Clinical expert in carotid artery disease
  • Physician & hospital staff training
  • Procedural case support
  • Gather clinical & best practice insights
  • Collaborate with internal stakeholders

Nice-to-have

  • Foster relationships with site investigators
  • Attend congresses or regional meetings
  • Work in a fast-paced environment
  • Operate as a team or independently

Key Requirements

  • Minimum 6 years Medtech experience
  • At least 3 years supporting interventional/surgical procedures
  • Knowledge of device clinical studies preferred
  • Ability to attain and maintain hospital credentials
  • Ability to stand for up to 8 hours wearing a lead apron

Work Rights

Not specified

Tailored Resume

Cover Letter