The Data Sharing Manager is responsible for managing and overseeing clinical data sharing requests, ensuring compliance with privacy standards and procedural requirements. The role involves supervising vendors, managing YODA Project requests, and supporting external research teams using J&J clinical data.
The Manager, Quality Clinical Risk Management role involves leading and participating in clinical trial risk management activities, including risk identification, mitigation, and escalation. The role also supports pre-submission quality reviews, inspection readiness, and provides guidance on quality and compliance issues.
This role involves leading the development and maintenance of product labeling documents, providing guidance on labeling content and processes, and contributing to the global labeling strategy. The position requires a strong understanding of regulatory affairs and pharmaceutical drug development, with a focus on ensuring high-quality and compliant labeling.
As an AI/ML/Data Science Intern, you will work on developing and implementing advanced AI methods for medical image and video understanding. Your responsibilities will include conducting interviews with clinical personnel, designing and evaluating computer vision models, and extracting insights from medical imaging data to improve clinical trial efficacy.
As an AI/ML/Data Science Intern, you will work on developing and implementing advanced AI methods for medical image and video understanding. You will collaborate with clinical personnel to understand their needs, design and evaluate computer vision models, and communicate technical insights to diverse stakeholders.
As an AI/ML/Data Science Intern, you will work on developing and implementing advanced AI methods for medical image and video understanding. Your responsibilities include conducting interviews with clinical personnel, designing and evaluating computer vision models, and extracting insights from medical imaging data to improve clinical trial efficacy.
The Principal Project Manager role involves coordinating and managing technical documentation and change notifications for EU Notified Bodies under the MDR. Responsibilities include project planning, risk management, stakeholder communication, and maintaining regulatory compliance. The role requires strong project management skills and experience in the medical device industry.
The Content Compliance Specialist role involves coordinating and moderating the copy approval process for advertising and promotional materials across the DePuy Synthes EMEA region. Key responsibilities include managing workflows, ensuring compliance, maintaining audit-ready records, and supporting continuous improvement initiatives.
The role involves managing and overseeing clinical data sharing requests, supervising vendors for data anonymization, and supporting external research teams. The position requires strong expertise in data sharing, privacy, and regulatory compliance.
This role involves leading the EMEA Supply Chain Technology - Logistics for DePuy Synthes, focusing on the regional technology roadmap, logistics platform management, and ensuring alignment with business priorities. The Senior Manager will partner with various teams to deliver technology solutions, manage operational reliability, and drive transformation initiatives while maintaining business continuity.
Leads safety evaluation and risk management for pharmaceutical products across development and post-marketing phases, providing scientific analysis to inform regulatory decisions and benefit-risk assessments. Works cross-functionally within Global Medical Safety to conduct proactive data reviews, support safety documentation, and guide strategy. Serves as subject matter expert and may oversee training, audits, and process improvements.
This role involves leading safety evaluations for pharmaceutical products in development and on the market, with a focus on analyzing complex medical data, supporting global safety teams, and ensuring regulatory compliance. The scientist will act as a subject matter expert, contribute to safety strategy, and provide oversight on critical safety documentation and risk management. Based in the U.S., the position operates in a hybrid model with significant autonomy and cross-functional collaboration.
This role involves leading the scientific safety assessment of pharmaceutical products across development and post-marketing stages, with a focus on analyzing complex medical data, supporting global safety teams, and ensuring regulatory compliance. The Associate Director will serve as a subject matter expert, driving safety evaluations, contributing to key clinical documents, and advising on risk management strategies. They will also lead training initiatives, support audits, and innovate processes for safety data interpretation and reporting.
The Medical Affairs Specialist supports the use of Intraocular Lenses (IOLs) through proctoring, case analysis, and managing Medical Information Requests (MIRs). They ensure optimal clinical outcomes by providing expert-level support to healthcare professionals and collaborating with various teams to analyze and optimize patient outcomes.
This role involves leading the scientific safety assessment of pharmaceutical products, supporting safety management teams, and ensuring regulatory compliance through high-quality safety evaluations and reporting. The individual will analyze complex medical-scientific data, contribute to risk-benefit assessments, and act as a subject matter expert during audits. The position emphasizes leadership, cross-functional collaboration, and innovation in safety data interpretation and presentation within a hybrid work environment.
