Senior Clinical Research Scientist

At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are our expertise in Innovative Medicine and MedTech we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow and profoundly impact health for more at .

As guided by Our Credo Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson we respect the diversity and dignity of our employees and recognize their merit.

Job Function:

Discovery & Pre-Clinical/Clinical Development

Job Sub Function:

Clinical Development & Research Non-MD

Job Category:

Scientific/Technology

All Job Posting Locations:

Danvers Massachusetts United States of America

Job Description:

We are searching for the best talent for Senior Clinical Research Scientist.

Fueled by innovation at the intersection of biology and technology were developing the next generation of smarter less invasive more personalized treatments.

Are you passionate about improving and expanding the possibilities of Cardiovascular Ready to join a team thats reimagining how we heal Our Cardiovascular team develops leading solutions for heart recovery electrophysiology and stroke. You will join a proud heritage of continually elevating standards of care for stroke heart failure and atrial fibrillation (AFib) patients.

Your unique talents will help patients on their journey to wellness. Learn more at is a hybrid role available in Danvers Massachusetts within the United States. While specific cities are listed in the Locations section for reference please note that they are examples only and do not limit your application. We invite candidates from any location to apply. Remote work options may be considered on a case-by-case basis and if approved by the Company.

Responsibilities:

• Support execution of Abiomeds scientific objectives within Abiomed-sponsored clinical studies
• Support protocol development revisions submission and approval including collaboration with study steering committee and principal investigators and communication with FDA
• Work closely with biostatistics team to evaluate study design options and analyze study data to support decisions related to protocol development and study execution

• Support the production of trial-related interim analyses hypothesis testing publications and presentations
• Provide scientific support for development of electronic data capture (EDC) for Abiomed-sponsored clinical studies

• Support planning and execution of steering committee meetings and investigator/research coordinator meetings
• Support generation of scientific content for study-related documents including annual and final study reports
• Review periodic study reports for outliers ranges and potentially problematic data; identify and communicate root causes and suggest possible solutions document data observations and follow pre-established processes and procedures
• Support execution of the regulatory pathway required for new investigational devices and for indication expansion globally
• Ensure data analysis integrity for clinical studies within scope of role
• Contribute to strong publication/presentation cadence for Abiomed-sponsored clinical studies

• Conduct literature review and clinical data review to support regulatory submissions and CERs
• Cross-collaboration with Medical Office and other departments

Qualifications:

• Advanced degree in science or engineering; MS PhD or MD required
• At least 3 years relevant post-graduate research experience
• Clinical science/research experience in cardiology/cardiovascular space or medical devices preferred
• Strong research background and publication history
• Strong understanding of biostatistics
• Proficient in statistical programming software (MATLAB R Python or SAS)
• Strong work ethic self-motivated team player with excellent English written and oral communication skills and strong interpersonal skills

Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race color religion sex sexual orientation gender identity age national origin disability protected veteran status or other characteristics protected by federal state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.

Johnson & Johnson is committed to providing an interview process that is inclusive of our applicants needs. If you are an individual with a disability and would like to request an accommodation please contact us via or contact AskGS to be directed to your accommodation resource.

The anticipated base pay range for this position is: $109000 - $174800.

The Company maintains highly competitive performance-based compensation programs. Under current guidelines this position is eligible for an annual performance bonus in accordance with the terms of the applicable plan. The annual performance bonus is a cash bonus intended to provide an incentive to achieve annual targeted results by rewarding for individual and the corporations performance over a calendar/performance year. Bonuses are awarded at the Companys discretion on an individual basis. Employees and/or eligible dependents may be eligible to participate in the following Company sponsored employee benefit programs: medical dental vision life insurance short- and long-term disability business accident insurance and group legal insurance. Employees may be eligible to participate in the Companys consolidated retirement plan (pension) and savings plan (401k).This position is eligible to participate in the Companys long-term incentive program. Employees are eligible for the following time off benefits: Vacation up to 120 hours per calendar year. Sick time - up to 40 hours per calendar year; for employees who reside in the State of Washington up to 56 hours per calendar year. Holiday pay including Floating Holidays up to 13 days per calendar year. Work Personal and Family Time - up to 40 hours per calendar year. For additional general information on Company benefits please go to: - This job posting is anticipated to close on August 28 2026. The Company may however extend this time-period in which case the posting will remain available on to accept additional applications.

Required Skills:

Preferred Skills:

Clinical Data Management Clinical Evaluations Coaching Critical Thinking Data Savvy Drug Discovery Development Ethical and Participant Safety Considerations Good Clinical Practice (GCP) Industry Analysis Medicines and Device Development and Regulation Regulatory Affairs Management Relationship Building Research Documents Safety-Oriented Scientific Research Standard Scientific Processes and Procedures Technologically Savvy