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- Tasks: Lead safety assessments and collaborate with teams to ensure product safety.
- Company: Join Johnson & Johnson, a leader in healthcare innovation dedicated to improving lives.
- Benefits: Enjoy a competitive salary, flexible working options, and career development opportunities.
- Why this job: Make a real impact in oncology by developing life-saving treatments and championing patient care.
- Qualifications: Degree in Healthcare/Biomedical Science with significant industry experience required.
- Other info: Hybrid work model available; remote options considered on a case-by-case basis.
The predicted salary is between 48000 - 72000 £ per year.
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.
About Innovative Medicine: 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.
About Oncology: Our Oncology team is focused on the elimination of cancer by discovering new pathways and modalities to finding treatments and cures. We lead where medicine is going and need innovators with an unwavering commitment to results.
The AD SAS provides scientific expertise and leads the safety assessment of assigned products and, 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. In summary, the AD SAS will support product Safety Management Teams (SMTs) and collaborate closely with cross-functional safety partners to determine a product’s safety strategy, conduct safety analyses, and lead safety data review meetings while interpreting safety information to make informed recommendations.
You will be responsible for:
- Take charge of strategy discussions, collaborating with the Therapeutic Area Safety Head (TASH), Medical Safety Office (MSO), and other key stakeholders.
- Handle data retrieval, analysis, report writing, and revisions to ensure comprehensive evaluations and guarantee high-quality reports with minimal comments and revisions from stakeholders.
- Provide valuable insights and reviews for key regulatory and clinical documents, supporting interactions with health authorities on safety and risk management through clear written and verbal communication.
- Show your leadership skills within the Safety Management Team (SMT) while supporting the MSO.
- Lead cross-functional training initiatives to improve stakeholder knowledge and skills.
- Lead proactive reviews of safety data to formulate a safety position utilisable for aggregate safety reports.
- Take on novel projects to build value and drive innovation, exploring creative ways to present data and prepare reports while improving efficiencies within your programmes.
- Act as a Subject Matter Expert (SME) during audits and inspections, while handling unscheduled reports within the Aggregate Report Calendar and overseeing deliverables prepared by team members, particularly complex reports.
- Participate in or spearhead departmental and cross-functional initiatives that promote teamwork and efficiency, encouraging management of activities within smaller Therapeutic Areas as applicable, along with overseeing contractor positions within your team when needed.
- Serve as backup to the TAL during their absence.
Qualifications / Requirements:
- A Degree in a Healthcare-related or Biomedical Science area with 11+ years industry experience is required, OR an advanced relevant degree (or higher) with 8+ years proven industry experience.
- Medical writing or PV experience.
- Solid understanding of medical concepts and familiarity with safety activities in drug development and post marketing and global safety health authority requirements.
- Ability to understand and analyse complex medical-scientific data from a broad range of disciplines is required.
- Ability to interpret and present complex data to determine benefit-risk impact is required.
- Ability to independently influence, negotiate and connect with both internal and external customers.
- Excellent English verbal and written communication.
- Ability to work in a matrix environment, proven leadership skills.
- Ability to plan work to meet deadlines and effectively handle multiple priorities.
Preferred:
- Clinical experience
- Early development submission experience
Benefits: We offer a competitive salary and extensive benefits package. The health and well-being of our employees is a priority; we have a flexible working environment as we value work-life balance. We offer career development opportunities for those who want to grow and be part of our organisation.
Associate Director, Safety Analysis Scientist, Oncology employer: Johnson & Johnson
Contact Detail:
Johnson & Johnson Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Associate Director, Safety Analysis Scientist, Oncology
✨Tip Number 1
Familiarise yourself with the latest trends and advancements in oncology and safety analysis. This will not only help you understand the role better but also allow you to engage in meaningful conversations during interviews, showcasing your passion and knowledge.
✨Tip Number 2
Network with professionals in the field of product safety and oncology. Attend relevant conferences or webinars, and connect with current employees at Johnson & Johnson on platforms like LinkedIn. This can provide you with insider insights and potentially a referral.
✨Tip Number 3
Prepare to discuss specific examples from your past experience that demonstrate your leadership skills and ability to influence stakeholders. Think about situations where you successfully managed complex projects or navigated challenging discussions.
✨Tip Number 4
Research Johnson & Johnson's recent initiatives in innovative medicine and oncology. Being able to reference their projects or values during your interview will show your genuine interest in the company and how you align with their mission.
We think you need these skills to ace Associate Director, Safety Analysis Scientist, Oncology
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in safety analysis, oncology, and any medical writing or pharmacovigilance roles. Use keywords from the job description to demonstrate your fit for the role.
Craft a Compelling Cover Letter: In your cover letter, express your passion for oncology and safety management. Discuss specific experiences that showcase your leadership skills and ability to influence stakeholders, as these are crucial for the role.
Highlight Relevant Qualifications: Clearly outline your educational background and industry experience, especially if you have a degree in a healthcare-related field. Mention any advanced degrees and how they relate to the position.
Showcase Communication Skills: Since excellent verbal and written communication is essential, provide examples of how you've effectively communicated complex data in previous roles. This could include reports, presentations, or interactions with health authorities.
How to prepare for a job interview at Johnson & Johnson
✨Understand the Role and Responsibilities
Before the interview, make sure you thoroughly understand the job description and responsibilities of the Associate Director, Safety Analysis Scientist role. Familiarise yourself with key terms related to safety analysis, regulatory compliance, and oncology to demonstrate your knowledge and enthusiasm.
✨Prepare for Technical Questions
Expect to be asked technical questions regarding safety assessment, data analysis, and medical writing. Brush up on your understanding of complex medical-scientific data and be ready to discuss how you would approach safety evaluations and risk management in drug development.
✨Showcase Your Leadership Skills
As this role involves leading cross-functional teams and training initiatives, be prepared to share examples of your leadership experience. Highlight situations where you influenced decisions or improved team performance, as this will resonate well with the interviewers.
✨Demonstrate Strong Communication Skills
Effective communication is crucial in this position. Practice articulating your thoughts clearly and concisely, both verbally and in writing. Be ready to discuss how you would communicate complex safety information to various stakeholders, including health authorities.
