Overview
On Site
Full Time
Skills
Training and development
Clinical trials
Public health
Pharmaceutical industry
Data Analysis
Clinical research
Leadership
Problem solving
Critical thinking
Strategy
Health care
Innovation
Spectrum
IMPACT
Design
Reporting
Research
Biostatistics
Marketing
Data
Collaboration
Science
Business analytics
Mergers and acquisitions
FOCUS
Epidemiology
Pharmaceutics
Presentations
Communication
Energy
SAP BASIS
Job Details
Description
Johnson & Johnson is currently seeking an Associate Director, Clinical Scientist to join our world-class Medical Affairs Gastroenterology Therapeutic Area Strategy Team located in Horsham, PA. Are you an ambitious Clinical Scientist looking to take your career to the next level? In this role, you will have the opportunity to work on groundbreaking projects and contribute to the development of life-changing medical breakthroughs.
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
In this role, you will contribute to world-class Medical Affairs sponsored and supported clinical programs for company products in the gastroenterology therapeutic area and make a significant impact on the lives of patients. As the Associate Director, Clinical Scientist, you will play a crucial role in the design, execution, analysis, and reporting of clinical studies, partnering closely with other GI team members, as well as real-world evidence, health economic and outcomes research, biostatistics, and commercial marketing personnel through integrated evidence teams. You will contribute to ways to identify and address key stakeholders' knowledge gaps through data dissemination, data generation, and education, through the design and execution of registries, Phase IIIb/IV trials and other post-marketing requirements within current or emerging US GI indications. Your expertise and proven track record will be essential in ensuring flawless execution of clinical trials and supporting the development of innovative therapies.
Participates in the development and execution of Medical Affairs sponsored and supported clinical programs for company products in the Gastroenterology Therapeutic Area
Supervises clinical studies of all types, including trials, registries, real-world evidence, collaborations and investigator-initiated studies
Participates in the preparation of regulatory submissions and presents and/or responds to questions at meetings with Health Authorities.
Collaborate closely with cross-functional teams to determine study objectives, design protocols, and develop clinical trial plans
Ensures regulatory post-marketing commitments are met with cost-effective, efficient and scientifically rigorous methods
Successfully implement innovative strategies to optimize clinical trial outcomes and accelerate the development timeline
Foster a culture of continuous learning and development within the clinical science team
Contributes to the development of abstracts and manuscripts related to Johnson and Johnson-supported and sponsored studies.
Builds and manages effective relationships with key opinion leaders and investigators related to Medical Affairs studies and initiatives
Qualifications
BA/BS required. MA/MS/PharmD/PhD preferred, ideally with focus on clinical science, public health, and/or epidemiology.
A minimum of 8 years total work experience required
Pharmaceutical industry experience required
Experience with data analysis and review and study medical monitoring is required
Clinical study, registry, or real-word evidence study experience strongly preferred
Demonstrated history of successfully designing and implementing clinical trials in the pharmaceutical or biotech industry preferred
Strong organizational abilities, presentation, written and verbal communication skills are required
Strong knowledge of regulatory guidelines and requirements for clinical research preferred
Energy and enthusiasm, strong leadership skills, and the ability and desire to embrace building subject matter expertise are essential
Exceptional problem-solving and critical-thinking abilities required
Ability to thrive in a fast-paced and highly collaborative environment required
Approximately 10% to 20% annual travel may be required (primarily domestic, occasionally international)
Don't miss this exciting opportunity to join a world-class team and contribute to the development of life-changing therapies. Apply now and take the next step in your career with Johnson & Johnson.
Johnson & Johnson is an Affirmative Action and 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, or protected veteran status and will not be discriminated against on the basis of disability.
Johnson & Johnson is currently seeking an Associate Director, Clinical Scientist to join our world-class Medical Affairs Gastroenterology Therapeutic Area Strategy Team located in Horsham, PA. Are you an ambitious Clinical Scientist looking to take your career to the next level? In this role, you will have the opportunity to work on groundbreaking projects and contribute to the development of life-changing medical breakthroughs.
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
In this role, you will contribute to world-class Medical Affairs sponsored and supported clinical programs for company products in the gastroenterology therapeutic area and make a significant impact on the lives of patients. As the Associate Director, Clinical Scientist, you will play a crucial role in the design, execution, analysis, and reporting of clinical studies, partnering closely with other GI team members, as well as real-world evidence, health economic and outcomes research, biostatistics, and commercial marketing personnel through integrated evidence teams. You will contribute to ways to identify and address key stakeholders' knowledge gaps through data dissemination, data generation, and education, through the design and execution of registries, Phase IIIb/IV trials and other post-marketing requirements within current or emerging US GI indications. Your expertise and proven track record will be essential in ensuring flawless execution of clinical trials and supporting the development of innovative therapies.
Participates in the development and execution of Medical Affairs sponsored and supported clinical programs for company products in the Gastroenterology Therapeutic Area
Supervises clinical studies of all types, including trials, registries, real-world evidence, collaborations and investigator-initiated studies
Participates in the preparation of regulatory submissions and presents and/or responds to questions at meetings with Health Authorities.
Collaborate closely with cross-functional teams to determine study objectives, design protocols, and develop clinical trial plans
Ensures regulatory post-marketing commitments are met with cost-effective, efficient and scientifically rigorous methods
Successfully implement innovative strategies to optimize clinical trial outcomes and accelerate the development timeline
Foster a culture of continuous learning and development within the clinical science team
Contributes to the development of abstracts and manuscripts related to Johnson and Johnson-supported and sponsored studies.
Builds and manages effective relationships with key opinion leaders and investigators related to Medical Affairs studies and initiatives
Qualifications
BA/BS required. MA/MS/PharmD/PhD preferred, ideally with focus on clinical science, public health, and/or epidemiology.
A minimum of 8 years total work experience required
Pharmaceutical industry experience required
Experience with data analysis and review and study medical monitoring is required
Clinical study, registry, or real-word evidence study experience strongly preferred
Demonstrated history of successfully designing and implementing clinical trials in the pharmaceutical or biotech industry preferred
Strong organizational abilities, presentation, written and verbal communication skills are required
Strong knowledge of regulatory guidelines and requirements for clinical research preferred
Energy and enthusiasm, strong leadership skills, and the ability and desire to embrace building subject matter expertise are essential
Exceptional problem-solving and critical-thinking abilities required
Ability to thrive in a fast-paced and highly collaborative environment required
Approximately 10% to 20% annual travel may be required (primarily domestic, occasionally international)
Don't miss this exciting opportunity to join a world-class team and contribute to the development of life-changing therapies. Apply now and take the next step in your career with Johnson & Johnson.
Johnson & Johnson is an Affirmative Action and 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, or protected veteran status and will not be discriminated against on the basis of disability.