At a Glance
- Tasks: Lead the creation of plain language summaries for clinical trial results, ensuring clarity and compliance.
- Company: Join Johnson & Johnson, a leader in healthcare innovation dedicated to improving lives.
- Benefits: Enjoy a competitive salary, extensive benefits, and opportunities for professional growth.
- Other info: Work in a diverse, inclusive environment with excellent career advancement opportunities.
- Why this job: Make a real impact on health by translating complex data into understandable insights.
- Qualifications: Bachelor’s degree in a scientific field and 5 years of relevant experience required.
The predicted salary is between 63000 - 77000 £ 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 Med Tech, 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: Data Analytics & Computational Sciences
- Job Sub Function: Data Governance & Policy
- Job Category: Professional
- All Job Posting Locations: High Wycombe, Buckinghamshire, United Kingdom
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 Med Tech, 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/.
We are searching for the best talent for a Manager Clinical Data Transparency / Plain Language Summary (PLS) Manager to join our Clinical Data Standards & Transparency team/ Innovative Medicine, to be located in High Wycombe / Maidenhead, United Kingdom; or Mumbai / Hyderabad, India.
Target start date: April/May 2027.
Please note that this role is available across multiple countries and may be posted under different requisition numbers to comply with local requirements.
While you are welcome to apply to any or all of the postings, we recommend focusing on the specific country(s) that align with your preferred location(s): United Kingdom - Requisition
Number: R-088079 India – Requestion
Remember, whether you apply to one or all of these requisition numbers, your applications will be considered as a single submission.
Purpose
The overall responsibility of the PLS Manager is to maintain the scientific integrity of clinical study results, aligned with J&J's compliance framework and regulatory standards, and deliver a summary that is understandable to lay readers in a fair, balanced, and non-promotional manner.
Proficiencies specific to the production of plain language summaries of clinical trial results
- Knowledge of the application of regulatory guidance (i. e., EU Clinical Trial Regulations) in writing PLSs
- Understands the principles of clinical research, fundamental biostatistics, and safety data reporting
- Interprets information for indications across various therapeutic areas using source documents such as the protocol, Clinical Study Report but also the Informed Consent Forms, Technical Summaries of Clinical Trial Results (i. e., Clinicaltrials. gov, Eudra CT)
- Applies critical scientific thinking to align the study rationale and research objectives with study endpoints and results.
- Understands the trial design, disease characteristics and measures being summarized to ensure study results accurately present scientific content in plain language
- Experience in writing Clinical Study Reports
- You will be responsible for
- Ensuring PLS production process is robust and scalable.
- Monitoring vendor quality to identify weak points and develop solutions
- Interacting effectively with multiple functions, clinical teams across all Therapeutic Areas and external vendors to communicate document requirements and to provide high quality results
- Ensuring compliance with departmental SOPs, Job Aids, policies and regulatory guidance documents
- Leading discussions by proposing solutions on guidelines, standards, processes
- Possessing sound organisational and leadership skills, and the ability to balance multiple responsibilities and work under tight time constraints
- Vendor oversight, reviewing all draft PLSs, ensuring adherence to PLS compliance documents (i. e., PLS Template and Job Aid) and health literacy principles
- Leading discussions with cross-functional teams to address and resolve content issues
- Completing understanding of J&J's PLS policy and regulatory mandates.
- Communicating effectively with team members to confirm studies qualify under internal policy and mandatory criteria (i. e., national and regional requirements including EU Clinical Trial Regulation [EU CTR])
- Assessing impact of and applying, as appropriate, regional and/or local PLS content-related requirements and evaluates the impact with key stakeholders
- Ensuring that results presentation is appropriate to the statistical analysis, and relevant for nonscientific readers, and includes sufficient context
- Understanding the concerns around commercially confidential information, intellectual property and participant privacy issues in clinical trials
- Collaborating with teams who publish clinical trial results for alignment
- Preparing material and facilitating meetings with PLS production extended team members (i. e., PLS and ad-hoc Subject Matter Experts)
- Facilitating the timely hand-off of PLS for translation to begin
- Attending and actively participating in vendor(s) operational and governance meetings, raising issues to PLS Lead
- Assisting in the updates of procedural documents, including the template, standard terms and definitions and Job Aids
- Identifying relevant program metrics to qualify/quantify project benefit, identifying risks and areas of improvement
- Possessing strong oral/written communication and presentation skills
- Mastering the use of systems, tools, and processes
Education & Experience Requirements
- A Bachelor’s degree in a scientific, technical or healthcare subject area, or equivalent experience is required.
- At least 5 years in relevant pharmaceutical/scientific experience in a related field; e. g. medical writing, PLS writing
- Excellent understanding of at least one of the following: regulatory clinical trial disclosure requirements, translation of scientific content for a lay audience
- Demonstrated written and verbal communications skills is required
- Demonstrated customer focus and solution-oriented experience required
- Proficient English written and spoken
- Ability to commence role April/May 2027
- Preferred
- Demonstrated interpersonal skills to build relationships with internal and external business partners
- Demonstrated leadership on cross-functional projects.
- Demonstrated leadership in strategic decision making and problem solving
Benefits
- We offer a competitive salary and extensive benefits package.
- We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment.
- Please contact us to request accommodation.
- Johnson & Johnson is an Affir…
Affirmative Action and Equal Opportunity Employer.
All qualified applicants will receive consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.
- Required Skills
- Clinical Data Analysis
- Clinical Data Interpretation
- Clinical Data Standards
- Preferred Skills
- Critical Thinking
- Cross-Functional Collaboration
- Data Privacy Standards
- Data Savvy
- Medical Writing
- Scientific Writing
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, andsolutions are personal.
Through our expertise in Innovative Medicine and Med Tech, 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/.
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Business Title Manager Clinical Data Transparency in High Wycombe employer: 7360-Janssen-Cilag Limited Legal Entity
Janssen-Cilag Limited is an exceptional employer that fosters a collaborative and innovative work culture in High Wycombe, England. With a strong commitment to employee development, we offer extensive growth opportunities through mentorship and training, ensuring our team members thrive in their careers while contributing to impactful clinical programming strategies. Our focus on operational excellence and compliance not only enhances the quality of our work but also creates a rewarding environment for those passionate about advancing healthcare.
Contact Details:
7360-Janssen-Cilag Limited Legal Entity Recruitment Team
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