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- Tasks: Lead safety signal detection and evaluation for innovative pharmaceutical products.
- Company: Join Johnson & Johnson, a leader in healthcare innovation.
- Benefits: Competitive salary, health benefits, and opportunities for professional growth.
- Why this job: Make a real impact on patient safety and healthcare solutions.
- Qualifications: Bachelor’s degree with experience in drug safety or related fields.
- Other info: Dynamic team environment with global collaboration and career advancement.
The predicted salary is between 48000 - 72000 £ per year.
Overview
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
Job Function
Product Safety
Job Sub Function
Pharmacovigilance
Job Category
Scientific/Technology
All Job Posting Locations
High Wycombe, Buckinghamshire, United Kingdom
Job Description
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.
Learn more at https://www.jnj.com/innovative-medicine
We are searching for the best talent for Associate Director, Signal Detection Scientist located in High Wycombe, UK.
The objective of this position is to lead the implementation of the Signal Management Group aggregate surveillance strategies for proactive and systematic detection and evaluation of new safety signals and emerging trends from post-marketing safety data for complex pharmaceutical products (e.g., large innovative programs, new therapeutic areas, or complex business partner relationships). These activities include the development, evaluation, piloting, and use of novel, computer-assisted tools and methodologies for signal detection and analysis of internal company safety data, international regulatory safety databases, and other data sources, e.g., claims and electronic medical records.
This position develops and implements product-specific surveillance plans, performs post-marketing signal detection activities, including signal validation, and participates in communication of emerging signals in forums, such as the Product Team Meetings and Safety Management Team Meetings. This position will also participate in the development of strategies for signal evaluation, including providing guidance on data sources and methods of analysis. The position may also perform activities supporting signal evaluation, such as ad hoc data mining of FDA FAERS, WHO VigiBase, and EMA EudraVigilance databases. The role also supports exploration of new signal detection methodologies, tools, and data sources to further the science of safety surveillance.
Primary Responsibilities
- Identify and assess (validate) new safety signals and trends by conducting systematic reviews of aggregate data with a focus on spontaneous adverse event reports. This includes signal detection activities in safety platforms, including our Company signal detection system and routine and ad hoc data mining in Empirica Signal.
- Prepare reviews of topics and summary analysis reports of safety data, with minimal guidance.
- Provide recommendations for further signal evaluation.
- Work with key customers and business partners (Medical Safety Officers, Safety Scientists, and other Safety Physicians) in developing and implementing product-specific surveillance plans.
- Participate as member of the matrix teams to address product specific safety issues, assist in the development of signal evaluation strategies, and participate in signal evaluation.
- Communicate findings from routine and ad hoc signal detection and assessment activities.
- Assist in the development and implementation of programmatic surveillance of adverse event reports for potential safety and product quality issues.
- Assist in the evaluation of novel, computer-assisted tools, and methodologies for analysis of safety data, including piloting new data source and methodologies.
Qualifications
Education:
- Bachelor’s Degree required
- Advanced Healthcare-related Degree (e.g., RN, BSN, PharmD) with 3+ years industry experience in drug safety or related area and 1+ year of clinical/patient-care experience highly preferred
Required
- Understanding of global health authority regulations and guidance surrounding the processing, reporting and evaluation of adverse events
- Understanding in single case medical assessment, post-marketing aggregate adverse event data reviews, evaluations of drug safety issues, adverse event dictionaries, core labeling, and Periodic Safety Review preparation
- Ability to lead projects
- Skillful in presenting complex data in a concise and understandable scientific manner
- Ability to thrive in a global, matrix environment – able to handle high workload and critical issues.
- Up to 10% travel – Domestic & International
Preferred
- Ability to manipulate data in platforms such as Excel and SAS JMP
- Familiarity with applied epidemiologic principles of case series evaluation and understanding of computer-assisted methodologies for safety data analysis
- Knowledge in public health surveillance and tools (relevant work experience or Masters Public Health or equivalent)
- Knowledge of statistics, or system analytics, information systems engineering, or machine learning
Required Skills
Preferred Skills:
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Associate Director, Signal Detection Scientist employer: Johnson & Johnson Innovative Medicine
Contact Detail:
Johnson & Johnson Innovative Medicine Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Associate Director, Signal Detection Scientist
✨Tip Number 1
Network like a pro! Reach out to professionals in the field of pharmacovigilance and signal detection. Attend industry events or webinars, and don’t be shy about asking for informational interviews. We all know that sometimes it’s not just what you know, but who you know!
✨Tip Number 2
Prepare for those interviews by brushing up on your knowledge of global health authority regulations and adverse event reporting. We recommend creating a cheat sheet of key concepts and examples from your experience. This will help you communicate your expertise clearly and confidently.
✨Tip Number 3
Showcase your analytical skills! Be ready to discuss how you've used data analysis tools like Excel or SAS in your previous roles. We suggest preparing a few case studies where you identified safety signals or trends, as this will demonstrate your hands-on experience.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we love seeing candidates who are proactive about their job search. So, get your application in and let’s make a difference in healthcare together!
We think you need these skills to ace Associate Director, Signal Detection Scientist
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Associate Director, Signal Detection Scientist role. Highlight your relevant experience in drug safety and any specific projects that align with the responsibilities mentioned in the job description.
Craft a Compelling Cover Letter: Your cover letter should tell us why you're passionate about healthcare innovation and how your background makes you a perfect fit for our team. Use specific examples to showcase your skills in signal detection and data analysis.
Showcase Your Skills: Don’t forget to highlight your technical skills, especially in data manipulation and analysis tools like Excel and SAS. We want to see how you can contribute to our mission of developing smarter treatments.
Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you’re considered for this exciting opportunity at Johnson & Johnson.
How to prepare for a job interview at Johnson & Johnson Innovative Medicine
✨Know Your Stuff
Make sure you brush up on your knowledge of pharmacovigilance and signal detection. Familiarise yourself with the latest regulations and guidance from global health authorities. Being able to discuss these confidently will show that you're serious about the role.
✨Showcase Your Analytical Skills
Prepare to discuss specific examples where you've successfully identified safety signals or trends from data. Use metrics and outcomes to illustrate your impact. This will demonstrate your ability to handle complex data and make informed decisions.
✨Be a Team Player
Since this role involves working in a matrix environment, be ready to talk about your experience collaborating with cross-functional teams. Highlight how you’ve contributed to team projects and how you handle differing opinions to achieve common goals.
✨Ask Insightful Questions
Prepare thoughtful questions about the company’s approach to innovative medicine and how they implement surveillance strategies. This shows your genuine interest in the role and helps you assess if the company aligns with your values and career goals.
