Associate Director, Clinical Science & External Research

6010-Biosense Webster Inc. Legal Entity; Irvine (CA); On-site; USD 137,000 - 236,000; Full time

Benefits offered by this job

Vacation time – 120 hours/year

Sick time – 40 hours/year

Parental Leave – 480 hours/year

Job summary

Johnson & Johnson MedTech Electrophysiology is recruiting an Associate Director, Clinical Science & External Research in Irvine, CA. Lead external research projects, ensure SOP/GCP compliance, and drive publication plans in collaboration with Clinical Research and Biostatistics teams.

You will mentor CSER staff, manage budgets, and liaise with diverse cross-functional teams to advance cardio-electrophysiology programs and evidence generation.

Qualifications

• Bachelor’s or Master’s Degree in Life Science or related field.
• PhD/MD/PharmD with 8–10 years of research experience preferred.
• Minimum 5+ years in clinical research or publication planning.

Responsibilities

• Leads end-to-end management of external research projects in CSER.
• Oversees clinical trial procedures and sponsor management.
• Develops and executes publication plans with cross-functional teams.
• Mentors CSER staff and manages project budgets.

Skills

Leadership

Clinical Operations

Clinical Research

Regulatory Knowledge

Biostatistics

Publication Planning

Written Communication

Project Management

Vendor Management

Team Mentoring

Education

Bachelor’s/Master’s in Life Science

PhD/MD/PharmD in relevant field

Job description

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through 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 humanity. Learn more at jnj.com 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:

R&D Operations

Job Sub Function:

Clinical/Medical Operations

Job Category:

People Leader

All Job Posting Locations:

Irvine, California, United States of America

Job Description: Johnson & Johnson MedTech Electrophysiology is recruiting for an Associate Director, Clinical Science & External Research to support the Electrophysiology (EP) business unit based in Irvine, CA. At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through 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 humanity. Learn more at https://www.jnj.com/. Fueled by innovation at the intersection of biology and technology, we’re 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 that’s 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 https://www.jnj.com/medtech.

Key Responsibilities:

• Leads end to end management of assigned external research projects ensuring compliance to SOPs, GCPs and study timelines
• Acts as a key leader from CSER responsible for clinical trial procedures, sponsor management and point of contact for internal and external meetings
• Leads publication plan development as well as execution in partnership with Clinical Research, Biostatistics and physician authors.
• Works with Clinical Study Team on data timelines to create long-term forecasting for data availability
• Enforce guidelines and Company policies governing the development of clinical data publications while continuing to look at innovation in publication and scientific communications
• Supports evidence generation strategy , by providing inputs and insights
• Provides input to publications, including substantial drafting and editing, as needed
• Provides status updates on assigned projects for management review
• Develops positive relationships with diverse cross-functional teams including Medical Affairs, Data Science, Health Economics and Market Access, Global Strategic Marketing, Education, Communications, etc.
• Develops subject matter knowledge and leads external scientific discussions and builds positive relationships with external physician partners
• Supports congress planning, as needed, including clinical booth activities and scientific sessions coverage
• Supervises and mentors team members and junior CSER staff
• Handles budget associated with assigned projects
• Leads or participates in monthly literature review with global teams; performs literature review as needed to support EGS and EDS

Qualifications:

• Education: A minimum of a Bachelor’s or Master’s Degree with at least 10-12 years of clinical, medical affairs or related technical experience, OR PhD/MD/ PharmD with 8-10 years of industry/academic research experience preferred. A Life Science, Physical Science, Nursing, or Biological Science degree.
• Required: Minimum of 5+ years of clinical research, clinical publication planning and writing experience in a medical industry or related setting. Leadership in managing teams in clinical research or evidence generation strategy. Able to influence others along with strong written and oral communication skills. Advanced project management skills with the ability to prioritize and balance multiple projects ensuring adequate follow through. Strategic mentality and critical analytical skill. Working knowledge of biostatistical methods. Excellent oral, written, and interpersonal communication skills. Knowledge of Good Clinical Practices and ICMJE standards.
• Preferred: Medical device experience, especially in cardiovascular and/or electrophysiology therapeutic experience highly preferred. Pre- or Postmarket study design and execution experience including clinical trial management. Experience with medical writing, publication planning. Other: This position will be located in Irvine, CA. May require up to 15% travel. Johnson & Johnson is an Equal Opportunity Employer.

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 https://www.jnj.com/contact-us/careers or contact AskGS to be directed to your accommodation resource.

Required Skills:

• Analytical Reasoning
• Clinical Operations
• Clinical Research and Regulations
• Clinical Trial Designs
• Clinical Trials
• Developing Others
• Fact-Based Decision Making
• Good Clinical Practice (GCP)
• Inclusive Leadership
• Innovation
• Laboratory Operations
• Leadership
• Operational Excellence
• Program Management
• Research and Development
• Research Ethics
• Team Management
• Vendor Management

Preferred Skills:

• Analytical Reasoning
• Clinical Operations
• Clinical Research and Regulations
• Clinical Trial Designs
• Clinical Trials
• Developing Others
• Fact-Based Decision Making
• Good Clinical Practice (GCP)
• Inclusive Leadership
• Innovation
• Laboratory Operations
• Leadership
• Operational Excellence
• Program Management
• Research and Development
• Research Ethics
• Team Management
• Vendor Management

Pay Transparency:

The anticipated base pay range for this position is : $137,000.00 - $235,750.00

Additional Description for Pay Transparency:

• Vacation –120 hours per calendar year
• Sick time - 40 hours per calendar year
• for employees who reside in the State of Colorado –48 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 – 480 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

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through 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 humanity. Learn more at https://www.jnj.com/.