Jobs at Johnson & Johnson

The Sr. Manager, Trial Delivery Leader oversees clinical trials, ensuring timely, budget-compliant delivery by managing cross-functional teams and operational plans while mitigating risks.

Lead development of Investigational Product Preparation and Administration Instructions (IPPI), ensure safe, compliant IP preparation and administration across clinical sites, provide CMC consultation, track portfolio milestones, drive process improvements, and mentor team members across therapeutic areas and development stages.

The Regional Account Manager will oversee clinical support and management of Shockwave's product portfolio, focusing on building relationships with healthcare professionals and facilitating access to new technologies.

The Associate Site Manager serves as the primary contact for trial sites, ensuring compliance with protocols and regulations. Responsibilities include site management, monitoring, recruitment strategy, and data accuracy, while maintaining strong relationships with internal and external partners.

The Manager, Standards Management Expert (ADaM) guides clinical data standards, manages projects, improves processes, and coaches junior colleagues while ensuring regulatory compliance.

The Senior Analytical Monitor will manage analytical monitoring activities for clinical trials, ensure compliance with regulations, and support site managers with data-driven insights and communication.

The Experienced Statistical Programmer supports data analysis and reporting activities, develops statistical programs, performs quality control, and collaborates with cross-functional teams to ensure timely and high-quality deliverables in clinical research.

The Principal Portfolio Lead in Clinical Programming is responsible for strategy formulation, execution of programming activities within clinical trials, and collaboration with stakeholders, ensuring high-quality standards and effective resource management.

The Sales Key Account Manager is responsible for driving revenue and market share growth in key orthopedic accounts, managing stakeholder relationships, providing clinical education, and ensuring effective product use.

The Associate Director, Safety Analysis Scientist is responsible for leading safety evaluations and assessments, managing safety data, and ensuring compliance with regulatory requirements in the area of product safety risk management.

The Senior Director, International HCC oversees compliance programs for DePuy Synthes internationally, ensuring adherence to healthcare laws and regulations. They coordinate resources, manage compliance risks, and engage with senior management to foster a culture of compliance while overseeing investigations and corrective actions.

The Senior Director leads the global Health Care Compliance risk management strategy, ensuring effective execution, governance, and oversight of compliance programs while partnering with senior leadership and managing global teams.

The Senior Manager Clinical Operations leads and manages early development and clinical trial operations, ensuring compliance, resource allocation, and staff performance management across multiple therapeutic areas.

The Experienced Clinical Programmer oversees clinical data management for trials, ensuring data accuracy and compliance with standards, while also developing reporting solutions and improving processes.

The Manager, Standards Management Expert oversees development and maintenance of clinical data standards, ensuring compliance and consistency in trials while coaching junior staff.