Job Function
Data Analytics & Computational Sciences
Job Sub Function
Clinical Data Management
Job Category
Professional
All Job Posting Locations
Allschwil Basel-Country Switzerland
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 are searching for the best talent for a Senior Manager Metrics Lead within Integrated Data Analytics & Reporting (IDAR) to guide the execution of projects programs and processes that span multiple related areas in support of the organizations overall Clinical Data Standards strategy.
Purpose
This position is responsible for applying comprehensive knowledge of Clinical Data Standards to install best in class policies procedures and plans for the area and ensuring consistency of clinical data standards across clinical trials and in compliance with regulatory requirements. The role tracks and analyzes metrics both Globally and across TAs to ensure the required level of standards use by trial teams. This position may be responsible for the development execution and maintenance of the governance framework across the clinical data lifecycle of standards development maintenance and implementation. The role works directly with governance councils and committees (i.e. Global council Therapeutic Area (TA) and Delivery Unit (DU) councils) to ensure adoption of standards leading development of content for review and ensuring decisions are made based on comprehensive understanding of standards and portfolio needs.
The role may be located in High Wycombe United Kingdom; Beerse Belgium; Leiden Netherlands; Allschwil Switzerland Titusville NJ / Raritan NJ / Spring House PA US (Hybrid / 3 days onsite per week preferred) .
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-046246
Belgium / Netherlands - Requisition Number : R-048174
Switzerland - Requisition Number : R-048176
United States - Requisition Number : R-048178
Remember whether you apply to one or all of these requisition numbers your applications will be considered as a single submission.
Responsibilities
Acting independently to facilitate programs and innovative initiatives for the organization to advance Clinical Data Standards solutions.
Working to achieve operational functional and business targets with measurable impact on results for the Clinical Data Standards area.
Developing processes to provide accurate timely and consistent clinical data standards to study teams.
Leading the implementation of new technologies for development and implementation of clinical data standards.
Guiding junior colleagues through consultation and mentoring in techniques and processes and provides functional (matrix) supervision.
Integrating Johnson & Johnsons Credo and Leadership Imperatives into team goals and decision making.
Principal Relationships
Internal : Align collaborate advise and share best practices with other functions and teams in Therapeutic Areas Global Development Regulatory Affairs Data Sciences Clinical Data Standards and others as needed.
External : Interact and collaborate with vendors. Act as J&J representative for defining process standards and sharing best practices with industry counterparts and working groups as required.
Are you ready to join our team Then please read further!
Education and Experience Requirements
A bachelors degree in a scientific technology or healthcare discipline or equivalent experience. Advanced degrees preferred (e.g. Master PhD)
At least 8 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
For United States applicants only
The expected base pay range for this position in the $137000 to $235750 (USD). The compensation and benefits information set forth in this posting applies to candidates hired in the United States. Candidates hired outside the United States will be eligible for compensation and benefits in accordance with their local market.
The Company maintains highly competitive performance-based compensation programs. Under current guidelines this position is eligible for an annual performance bonus in accordance with the terms of the applicable plan. The annual performance bonus is a cash bonus intended to provide an incentive to achieve annual targeted results by rewarding for individual and the corporations performance over a calendar / performance year. Bonuses are awarded at the Companys discretion on an individual basis.
Subject to the terms of their respective plans employees and / or eligible dependents are eligible to participate in the following Company sponsored employee benefit programs : medical dental vision life insurance short and long-term disability business accident insurance and group legal insurance.
Subject to the terms of their respective plans employees are eligible to participate in the Companys consolidated retirement plan (pension) and savings plan (401(k)). This position is eligible to participate in the Companys long-term incentive program. Subject to the terms of their respective policies and date of hire employees are eligible for the following time off benefits :
Vacation 120 hours per calendar year
Sick time - 40 hours per calendar year; for employees who reside in the State of Colorado 48 hours per calendar year; for employees who reside in the State of Washington 56 hours per calendar year
Holiday pay including Floating Holidays 13 days per calendar year
Work Personal and Family Time - up to 40 hours per calendar year
Parental Leave 480 hours within one year of the birth / adoption / foster care of a child
Bereavement Leave 240 hours for an immediate family member : 40 hours for an extended family member per calendar year
Caregiver Leave 80 hours in a 52-week rolling period 10 days
Volunteer Leave 32 hours per calendar year
Military Spouse Time-Off 80 hours per calendar year
For additional general information on company benefits please go to : job posting is anticipated to close on January 5 2026. The Company may however extend this time-period in which case the posting will remain available on to accept additional applications.
Equal Opportunity Employer and Disability Accommodation
Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race color religion sex sexual orientation gender identity age national origin disability protected veteran status or other characteristics protected by federal state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.
Johnson & Johnson is committed to providing an interview process that is inclusive of our applicants needs. If you are an individual with a disability and would like to request an accommodation external applicants please contact us via internal employees contact AskGS to be directed to your accommodation resource.
Required Skills
Clinical Data Standards Decision Making Project Management Leadership
Preferred Skills
Advanced Analytics Clinical Data Management Clinical Trials Operations Data Privacy Standards Data Quality Data Savvy Good Clinical Practice (GCP) Innovation Issue Escalation Learning Management Systems (LMS) Leverages Information Organizing Program Management Regulatory Affairs Management Research Ethics Technical Credibility
Required Experience
Senior Manager
Key Skills
Administrative Skills,Facilities Management,Biotechnology,Creative Production,Design And Estimation,Architecture
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