
Healthcare Insurance • Pharmaceuticals • Biotechnology
Johnson & Johnson is a multinational corporation focused on innovating across multiple sectors of healthcare and medicine. With a commitment to redefining healthcare, the company merges science and technology to address complex diseases through its divisions in innovative medicine and medical technology. Its areas of focus include oncology, immunology, neuroscience, and specialty ophthalmology, as well as interventional solutions and orthopaedics. J&J is dedicated to advancing global health equity and environmental sustainability while fostering innovation, diversity, and inclusion in the workplace. The company strives to provide solutions that connect health and care for providers, patients, and communities worldwide.
10,000+ employees
Founded 1886
⚕️ Healthcare Insurance
💊 Pharmaceuticals
🧬 Biotechnology
14 hours ago

Healthcare Insurance • Pharmaceuticals • Biotechnology
Johnson & Johnson is a multinational corporation focused on innovating across multiple sectors of healthcare and medicine. With a commitment to redefining healthcare, the company merges science and technology to address complex diseases through its divisions in innovative medicine and medical technology. Its areas of focus include oncology, immunology, neuroscience, and specialty ophthalmology, as well as interventional solutions and orthopaedics. J&J is dedicated to advancing global health equity and environmental sustainability while fostering innovation, diversity, and inclusion in the workplace. The company strives to provide solutions that connect health and care for providers, patients, and communities worldwide.
10,000+ employees
Founded 1886
⚕️ Healthcare Insurance
💊 Pharmaceuticals
🧬 Biotechnology
• Create and update critical trial-specific documents (e.g., Monitoring Guidelines, Informed Consent Form, Investigational Medicinal Product [IMP] related documentation). • Vendor set up and management of day-to-day study vendor activities, including set-up, SOW creation and budget oversight. • Responsible for country / regional coordination of trial management activities and oversight (e.g., aligns feasibility strategy with local teams, perform country-level risk reviews, aware of all projects conducted across countries). • Support development of program-level compound training, collaborating with Clinical / CTL&D Medical writing. • Provide input into trial level operational strategies. • Resolve trial-related issues and mitigate trial-related risks. • Participate in process improvement activities at a trial, compound & cross-DU level, as needed. • Provide support during Health Authority inspections and on the identification of risks and mitigation plans at the program level for key issues. • Mentor & support onboarding of new team members, particularly those in Trial Management. • Foster employee engagement, inclusion, and Credo Behaviors.
• A minimum of a BS degree or equivalent, preferred areas of study include Life Sciences (Life Sciences (e.g., Biology, Chemistry, Biochemistry, Nursing, Pharmacy). • A minimum of 8 years in Pharmaceutical, Healthcare or related industries. • Experience in and knowledge of the pharmaceutical development process. • Clinical research operational knowledge and experience across multiple phases of studies (Phase I-IV) must have the ability to manage all aspects of execution of a clinical trial. • 2-3 years’ experience leading multiple aspects of a global clinical trial. • Must possess excellent leadership skills and proven ability to foster team productivity and cohesiveness. • Experience of leading without authority and in muti-functional matrixed and global environments. • Excellent decision-making, analytical and strong financial management skills are essential to this position. • Operate and execute with limited supervision. • Experience mentoring/coaching others. • Strong project planning/management, communication and presentation skills are required. • Travel up to 15-20% of the time, defined by business needs.
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