Job Function:
Medical Affairs Group
Job Sub Function:
Medical Affairs
Job Category:
Scientific/Technology
All Job Posting Locations:
Irvine, California, United States of America
Job Description:Job Summary:
This Medical Affairs Senior Scientist will be responsible for supporting one or several product development projects within the JJMT EP’s product portfolio while fostering strong, productive relationships with colleagues across the organization.
Duties and Responsibilities:
- Responsible for executing the pre-clinical strategy to support product characterization and design features
- Will develop and execute product and/or procedural protocols for evidence generation
- Collaborate with evidence generation colleagues for evidence generation for new and existing products to support regulatory approval/clearance
- Provide scientific and test method expertise during study design development
- Provide pre-clinical insight to the development teams for the risk assessment
Education
- Recommended, but not required: BSwith at least 6 years, MS with at least 4 years, PhD with at least 2 years of relevant experience in Engineering, Life Sciences, Physical Sciences, Nursing, or Biological Science. Pre-clinical experience working at a CRO operating on swine/canine models with surgical experience including necropsy.
Experience
- An understanding of cardiac anatomy and medical devices is required.
- A minimum of 3 years working on pre-clinical models is required, with chronic models is preferred.
- Advanced technical writing skills are required with an emphasis on organizing data and presenting findings, with demonstrated success in medical data generation, interpretation, and publications are highly preferred
- A proven working knowledge of catheter laboratory equipment and operating room procedures
- Experience in working with global cross-functional teams is required.
- Must be able to work in a high stress environment with minimal supervision.
- Proven project management skills, with a demonstrable track record of success managing multiple projects
- Must be able to collaborate well with multiple partners and work effectively in a matrix environment
Required Skills:
Preferred Skills:
Analytical Reasoning, Clinical Research and Regulations, Clinical Trials Operations, Coaching, Collaboration, Communication, Critical Thinking, Data Analysis, Data Savvy, Digital Culture, Digital Literacy, Healthcare Trends, Medical Affairs, Medical Communications, Medical Compliance, Product Development Lifecycle, Report Writing, Stakeholder Engagement, Technologically Savvy
The anticipated base pay range for this position is :
$109,000.00 - $174,800.00
Additional Description for Pay Transparency:
Subject to the terms of their respective policies and date of hire, employees are eligible for the following time off benefits:
Vacation 120 hours per calendar year
Sick time - 40 hours per calendar year; for employees who reside in the State of Colorado 148 hours per calendar year; for employees who reside in the State of Washington 56 hours per calendar year
Holiday pay, including Floating Holidays 13 days per calendar year
Work, Personal and Family Time - up to 40 hours per calendar year
Parental Leave 180 hours within one year of the birth/adoption/foster care of a child
Bereavement Leave 240 hours for an immediate family member: 40 hours for an extended family member per calendar year
Caregiver Leave 80 hours in a 52-week rolling period10 days
Volunteer Leave 32 hours per calendar year
Military Spouse Time-Off 80 hours per calendar year
For additional general information on Company benefits, please go to: - https://www.careers.jnj.com/employee-benefits
