- Insmed Incorporated (NJ)
- …vendors for clinical services, management of project timelines and deliverables. Key global trial management support to the Associate Directors (CST Leads), ... so does every person who joins in. As a global biopharmaceutical company dedicated to transforming the lives of...contributions to meaningful progress. That commitment has earned us recognition as Science magazine's No. 1 Top Employer for… more
- Terumo Neuro (Aliso Viejo, CA)
- **13097BR** **Title:** Sr . Manager, Environmental Health & Safety (EHS) **Job Description:** Play a pivotal role in shaping and leading EHS initiatives at ... + Work closely with EHS leaders at other MicroVention sites to incorporate global and local safety best practices and formulate a comprehensive Business Continuity… more
- Jazz Pharmaceuticals (Redwood City, CA)
- …Jazz employee please apply via the Internal Career site. Jazz Pharmaceuticals is a global biopharma company whose purpose is to innovate to transform the lives of ... achieve compliance, inspection readiness, and continuous improvement across the Regulatory and Labeling organizations. Essential Functions/Responsibilities Responsible for all… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …understanding of professional working environment as well as Quality Assurance and global regulatory requirements such that identification of risks is recognized ... oriented in the execution of processes, as directed by senior staff, playing a supportive role in ensuring adherence...Import/export requirements to the extent that there is overall recognition of global differences exist and understanding… more
- Insmed Incorporated (San Diego, CA)
- …the future of science, we're in. Are you?About the Role:Insmed is seeking a Senior Research Associate - Lab Technician with specialized expertise in supporting ... so does every person who joins in. As a global biopharmaceutical company dedicated to transforming the lives of...contributions to meaningful progress. That commitment has earned us recognition as Science magazine's No. 1 Top Employer for… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …research areas centered around rare diseases and immune disorders. Summary The Associate Director, Global Oncology Medical Affairs, Medical Analytics will be ... for cardiovascular diseases, under the Group's 2025 Vision to become a " Global Pharma Innovator with Competitive Advantage in Oncology," Daiichi Sankyo is primarily… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …for cardiovascular diseases, under the Group's 2025 Vision to become a " Global Pharma Innovator with Competitive Advantage in Oncology," Daiichi Sankyo is primarily ... clinical studies, under the supervision of the Study Manager role the Study Associate Manager within Clinical Operations, in adherence to the protocol, Good Clinical… more
- Oatey (Shakopee, MN)
- …Sigma, and continuous improvement. + Strong knowledge of quality systems and global regulatory compliance requirements. + Demonstrated business and financial ... make an impact in a place where you matter?** **Position Summary:** The Senior Director, Cherne Global Operations will provide strategic leadership and oversight… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …for cardiovascular diseases, under the Group's 2025 Vision to become a " Global Pharma Innovator with Competitive Advantage in Oncology," Daiichi Sankyo is primarily ... research areas centered around rare diseases and immune disorders. Summary The Associate General Counsel, Intellectual Property is responsible for the protection of… more
- Merck & Co. (Upper Gwynedd, PA)
- …create breakthrough science that radically changes the way we approach serious diseases. --The Senior Director will report to an Associate Vice President in the ... Job DescriptionOur company is a global health care leader with a diversified portfolio...regulatory reporting, and publication. -- Responsibilities: Specifically, the Senior Director may be responsible for: -Analyzing and summarizing… more
- Jazz Pharmaceuticals (Palo Alto, CA)
- …Jazz employee please apply via the Internal Career site. Jazz Pharmaceuticals is a global biopharma company whose purpose is to innovate to transform the lives of ... member of the REMS Strategy and Operations department, the Senior Manager, REMS Data Programmer will provide support for...product risk management initiatives. This role reports to the Associate Director, REMS Analytics and Reporting level of the… more
- Olympus Corporation of the Americas (Center Valley, PA)
- …Learn more about Life at Olympus: https://www.olympusamerica.com/careers . **Job Description** The Sr . Clinical Trial Coordinator ( Sr . CTC) will be responsible ... of a clinical study by carrying out day-to-day study activities. The Sr . CTCwill develop, implement, and coordinate study procedures to successfully manage clinical… more
- Sun Pharmaceuticals, Inc (Princeton, NJ)
- …(GDP), and ALCOA++ principles. The role also provides support during regulatory , corporate, and internal audits. **Key Responsibilities** + Support batch ... preventive actions are appropriate and effective. + Ensure compliance with regulatory requirements for product, process, equipment, and release procedures. + Provide… more
- BeOne Medicines (San Mateo, CA)
- …medical devices - Conduct site visits to determine protocol and regulatory compliance, and prepare required documentation - Develop collaborative relationships with ... clinical trial processes with a thorough knowledge of ICH and associated regulatory guidelines - Minimum of 4-6 years of relevant Clinical Operations experience… more
- SMBC (New York, NY)
- …models, ensuring appropriate design and use. + Align model frameworks with business objectives and regulatory requirements ( SR 11-7, SR 12-7, SR 15-18, ... SMBC Group is a top-tier global financial group. Headquartered in Tokyo and with...seeks a quantitatively oriented individual for the position of Associate , Quantitative Analytics within Corporate Treasury. The role involves… more
- Lundbeck (Deerfield, IL)
- …and KOL relationships and collaborating with other functions (eg, Value Evidence, Regulatory , Clinical Development, Brand Teams, Global Medical Affairs etc.) in ... Associate Director Medical Affairs - Neurology Requisition ID:...including late stage and pipeline products + Collaborate with global Medical Affairs and cross-functional teams ( Regulatory ,… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …we work together to change lives for the better. The Position The Associate Director, Media Relations & Issues Management is accountable for establishing and leading ... the Director, Media & Stakeholder Relations, and interacts with senior leaders across all areas of Novo Nordisk US...Affairs, Legal, Finance and Investor Relations, Clinical, Medical and Regulatory , plus other cross functional teams as needed. Key… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …we work together to change lives for the better. The Position The Associate Director, Consumer Social Media Strategy is a high-impact, hands-on leadership role ... This role translates the corporate digital vision set by the Senior Director into best-in-class digital experiences, driving audience engagement, building brand… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- Legend Biotech is a global biotechnology company dedicated to treating, and one day curing, life-threatening diseases. Headquartered in Somerset, New Jersey, we are ... and cutting-edge therapeutics for patients worldwide.Legend Biotech entered into a global collaboration agreement with Janssen, one of the pharmaceutical companies… more
- Cipla (Central Islip, NY)
- …posting for local applicants only - is not for those applying for a global assignment and/or for employees working outside of Cipla's US Subsidiaries or Affiliates ... Job Title SCM Procurement- Associate Buyer Organization Name Invagen - A Cipla subsidiary...contracts. Suppliers - cost negotiation, material procurement, technical support, Regulatory docs for custom clearance, permits, approvals etc Service… more
