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 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: **
Clinical Data Management
Job Category:
Professional
All Job Posting Locations:
Beerse, Antwerp, Belgium, Leiden, South Holland, Netherlands
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 a** Manager, Standards Management Expert (ADaM)** within Integrated Data Analytics & Reporting (IDAR), to provide expert guidance and tailored solutions on projects, programs, and processes that span multiple related areas in support of the organization's overall Clinical Data Standards strategy. The Standards Management Expert (ADaM) is an individual contributor who takes a leadership role in the collaboration with various internal and external partners to ensure consistency of clinical data standards across clinical trials and in compliance with regulatory requirements.
**This role may be located in High Wycombe, United Kingdom, Beerse, Belgium or Leiden, Netherlands (Hybrid / 3 days onsite per week preferred). **
Please note that this role is also 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):
Belgium/Netherlands- Requisition Number: R-047957
United Kingdom - Requisition Number: R-046150
Remember, whether you apply to one or all of these requisition numbers, your applications will be considered as a single submission.
Purpose:
- Acts as a top-level specialist to establish programs and innovative strategies that advance the Clinical Data Standards organization
- Manages standards, projects, programs, or processes for Clinical Data Standards in line with agreed internal strategy and regulatory requirements.
- Participates in the development of solutions to provide accurate, timely, and consistent clinical data standards to study teams.
- Communicates ideas for process improvement, while supporting the design and integration of new technologies to enhance clinical data standards.
- Coaches and trains junior colleagues in clinical data standards application and responsibilities.
- Integrates Johnson & Johnson’s Credo and Leadership Imperatives into team goals and decision making.
You will be responsible for:
Manager, Standards Management Expert (ADaM) is responsible for the development and maintenance of clear specifications for standard content across the data lifecycle, including data collection, delivery, analysis & reporting, aligned with program requirements and medical writing. Examples of standard content:
- Analysis Data Model metadata (ADaM)
- Template spreadsheets for adverse events and medications of interest, laboratory toxicities/abnormalities.
The role is responsible for acquiring and maintaining deep expertise in the various data collection and analysis tools and templates applied in the clinical trials, specifically those in use in J&J (e.g., AUTOCODE), in industry standards, including but not limited to CDISC standards (ADaM and define.xml) and adjacent data standards (e.g., HL7 / FHIR, OHDSI/OMOP).
The role should be knowledgeable in using common clinical data tools such as LSAF, Pinnacle 21, or SAS. The position may also be involved in innovative projects which requires learning of new tools and standards.
The role is responsible for remaining aware of the industry standards development and trends, and regulatory requirements, to support the development strategy and evolution of the J&J.
The role may also have responsibility for providing operational expertise in cross functional initiatives
Qualifications / Requirements:
- A Bachelor’s degree in a scientific, technology or healthcare discipline, or equivalent experience. Advanced degrees preferred (e.g., Master, PhD)
- At least 6 years of relevant pharmaceutical/scientific experience in a related discipline; e.g., data management, biostatistics, clinical or statistical programming
- Expert knowledge of relevant regulatory requirements (e.g., GCP, ICH) and industry standards (e.g., SDTM, ADaM)
- Demonstrated written and verbal communications skills
- Demonstrated customer focus and solution-oriented experience
- Demonstrated interpersonal skills to build relationships with internal and external business partners
- Demonstrated leadership on cross-functional projects
- Demonstrated leadership in decision making and problem solving
- Excellent spoken and written English
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.
Johnson & Johnson Family of Companies are equal opportunity employers, and all qualified applicants will be considered for employment without regard to any other characteristic protected by law. We will ensure that individuals with disabilities are provided a reasonable accommodation to participate in the job application or interview process, to perform crucial job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.
#LI-Hybrid
**Required Skills: **
Clinical Data Standards, Data Analysis Reporting, Data Collection Methods
Preferred Skills:
Biostatistics, CDISC ADaM, Clinical Data Interchange Standards Consortium (CDISC) Standards, Clinical SAS Programming, Cross-Functional Leadership, Data Management, Regulatory Requirements, Statistical Programming