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Clinical Documentation Coordinator – 2406195241W
Description
An internal pre-identified candidate for consideration has been identified. However, all applications will be considered.
About Johnson & Johnson
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/.
Are you ready to be a crucial part of our mission to build a world without disease? Janssen Research & Development, a proud member of the Johnson & Johnson Family of Companies, is on the lookout for a dynamic individual to join our team as a Clinical Documentation Coordinator based in Beerse, Belgium.
About the Role: As a member of our Clinical Pack & Tech department, situated within the global Janssen Research & Development organization, you will play a vital role in our commitment to clinical excellence. Working in close collaboration with a team of Clinical Documentation Coordinators, you will be responsible for creating clinical labels and batch records.
Key Responsibilities:
Execute packaging and labeling activities for a diverse portfolio of clinical studies.
Serve as the Single Point of Contact (SPOC) for the Clinical Source Documentation Specialist, operations, and Local Medication Coordinators.
Collaborate with various CSC functions to ensure seamless processes.
Apply NGENCODAC for label and order creation, ensuring compliance with source documentation, local requirements, and technical specifications.
Timely upload of approved labels into submission database, adhering to system requirements and naming conventions.
Qualifications
Bachelor’s degree or equivalent through experience.
Result and performance-driven mentality.
Ability to thrive in a cross-cultural environment and multidisciplinary teams.
Proactive and independent, with a collaborative spirit.
Knowledge and experience with GMP activities and GDP guidelines.
Specific expertise in Clinical Packaging & Label requirements is a valuable asset.
Preferred:
Enthusiasm for working on multiple projects simultaneously.
Passion for delivering precision work; excellence is non-negotiable.
Thrives on tackling innovative, complex issues and simplifying them.
Critical thinking ability and leadership skills in inspiring change and optimization.
Johnson & Johnson is an Affirmative Action and 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, or protected veteran status and will not be discriminated against on the basis of disability.
Primary Location Europe/Middle East/Africa-Belgium-Antwerp-Beerse
Organization Janssen Pharmaceutica N.V. (7555)
Job Function Clinical Supply Operations
Req ID: 2406195241W
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