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Submissions & Regulatory Intelligence Manager

Job in High Wycombe, Buckinghamshire, HP13, England, UK
Listing for: 7360-Janssen-Cilag Limited Legal Entity
Full Time position
Listed on 2026-10-08
Job specializations:
  • Healthcare
    Healthcare Management, Healthcare Compliance
Salary/Wage Range or Industry Benchmark: 90000 - 130000 GBP Yearly GBP 90000.00 130000.00 YEAR
Job Description & How to Apply Below
Company Overview

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, 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  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

Job Posting Location

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

Position Overview

We are searching for the best talent for a Submissions & Regulatory Intelligence Manager within Integrated Data Analytics & Reporting (IDAR), to contributes to the Clinical Data Standards team as an individual contributor and a developing subject matter expert, to take a leadership role in the collaboration with various internal and external partners. The Submissions & Regulatory Intelligence Manager provides expert guidance and implements tailored solutions on projects, programs, and processes that span multiple related areas in support of the organization’s overall Clinical Data Standards strategy.

Foremost is ensuring consistency of clinical data standards across clinical trials and in compliance with regulatory requirements.

Location Options

This role may be located in High Wycombe/Maidenhead, United Kingdom;
Beerse, Belgium;
Allschwil, Switzerland;
Leiden, Netherlands; or Spring House/Raritan/Titusville, United States (Hybrid / 3 days onsite per week preferred).

Requisition s
  • Belgium/Netherlands
    - Requisition Number: R-103242
  • United Kingdom
    - Requisition Number: R-101253
  • Switzerland
    - Requisition Number: R-103247
  • United States
    - Requisition Number: R-103251
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.

Key Responsibilities

The Submissions & Regulatory Intelligence Manager is responsible for providing significant expertise to the IDAR department (and GD if applicable) in clinical study data regulatory submission requirements and strategies. Examples of this content are:

  • Newly released or updated Regulatory Health Authority (RHA) and industry guidance documentation
  • Identification of…
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