Associate Director, Safety Analysis Scientist

Biopharma Careers; Horsham (PA); On-site; USD 150,000 - 180,000; Full time

Job summary

Johnson & Johnson Horsham, PA, is seeking an Associate Director, Safety Analysis Scientist to lead scientific safety analyses for products from development through lifecycle.

You will partner with Medical Safety Officers and SMTs to shape safety strategy, review data, and prepare regulatory submissions while guiding cross-functional teams on complex reports.

Qualifications

• Advanced degree in a relevant field (PhD/MD/PharmD) preferred.
• Extensive experience in safety data review and regulatory submissions.
• Strong communication and leadership skills for cross-functional teams.

Responsibilities

• Lead safety assessment and scientific safety analyses for assigned products.
• Collaborate with SMTs and cross-functional safety partners to shape product safety strategy.
• Review safety data and lead safety data review meetings.
• Provide training and oversight for junior team members on complex reports.

Skills

Safety analysis

Cross-functional collaboration

Regulatory compliance

Medical safety

Job description

# Associate Director, Safety Analysis ScientistHorsham, United States Full timeOther / Corporate Functions Associate DirectorNotify me about similar jobsView Full Job & Apply at Johnson & JohnsonJohnson & Johnson is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.## About this opportunityAt 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.comAs 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:**Product Safety**Job Sub Function:**Product Safety Risk Management**Job Category:**Scientific/Technology**All Job Posting Locations:**Horsham, Pennsylvania, United States of America, Raritan, New Jersey, United States of America, Titusville, New Jersey, United States of America**Job Description:**Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow.Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.Learn more at https://www.jnj.com/innovative-medicine**We are searching for the best talent for Associate Director, Safety Analysis Scientist.**The Associate Director (AD) Safety Analysis Scientist (SAS) provides scientific expertise and leads the safety assessment of assigned products. The AD SAS, in partnership with the Medical Safety Officer (MSO), is responsible for the preparation of scientific safety analysis and evaluations, which are required for regulatory compliance and to aid in safety-related decisions for marketed products and products in development.The AD SAS will support product Safety Management Teams (SMTs) and work in close collaboration with other cross-functional safety partners to determine a product’s safety strategy, complete safety analyses and evaluations, proactively review safety data/lead safety data review meetings and interpret safety information to make a recommendation, supporting SMT deliverables as required.The AD SAS will assist the Medical Safety Officer (MSO) with activities related to the SMT and with contributions to key safety and clinical documents.The AD SAS will have in-depth product knowledge, will serve as product point of contact, and will provide training to, and oversight of deliverables prepared by, other team members as needed (for complex reports).