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Pharmaceutical jobs in Parsippany, NJ

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Eli Lilly and Company - Stamford, CT
Oncology Sales Representatives will be responsible for dissemination of clinical information about Lilly Oncology's products and services for patients with cancer to healthcare professionals including medical oncologists, oncology nurses, office managers, reimbursement manager, and pharmacists. Primary responsibility will be for CYRAMZA (ramicirumab) and ALIMTA (pemetrexed). The selling approach requires strong scientific ..


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Sr. Technical Training Specialist
Morris Plains, NJ
Job Description This role is responsible for preparing, conducting and evaluating technical training programs and will partner with technical subject-matter experts (SMEs) to conduct training needs assessments, develop and provide hands-on training support to effectively design, develop, deliver and measure training related to our Quality Systems and GMP training requirements. This ..

Last verified - 1 day(s) 5 hour(s) ago



Technical Training Specialist
Morris Plains, NJ
This role is responsible for preparing, conducting and evaluating technical training programs and will partner with technical subject-matter experts (SMEs) to conduct training needs assessments, develop and provide hands-on training support to effectively design, develop, deliver and measure training related to our Quality Systems and GMP training requirements. • Prepare and ..

Last verified - 1 day(s) 5 hour(s) ago



Sr. QA Compliance Specialist (Audit and Self-Inspection)
Morris Plains, NJ
PURPOSE • Responsible for management and oversight of Morris Plains Self-Inspection Program. • Oversight and monitoring of Novartis, BTDM Compliance and Alert actions for compliant CGT implementation • Oversight of actions and CAPAs associated with GCA audits and HA inspections for compliant implementation. • Support Global Compliance initiatives, departmental projects and ..

Last verified - 1 day(s) 4 hour(s) ago



Associate Director, QA Validation
Morris Plains, NJ
The incumbent will focus in development, implementation, validation standard and strategy of analytical methods, automation systems, cleaning, laboratory instrument, equipment, utilities, and process in adherence to Corporate policies, standards, and government regulations. This role will provides vision, guidance, direction, and consultations to system users, quality control and manufacturing department personnel, and ..

Last verified - 1 day(s) 5 hour(s) ago



Associate Director, Strategic Market Access CAR-T
East Hanover, NJ
The role will report to the Executive Director, Market Access CAR-T and will be responsible for Oncology Market Access deliverables with the CAR-T Business Franchises (BF) and the CTL019 Brand team. They will support and collaborate to: • Establish new product value propositions inclusive of pricing, patient access and distribution • ..

Last verified - 1 day(s) 4 hour(s) ago


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Senior Investigator – Clinical Pathologist
East Hanover, NJ
Summary The clinical pathologist provides expertise to research and preclinical safety studies through well-written reports that accurately reflect data derived from standard clinical pathology endpoints as well as investigative biomarkers and immunotoxicological assessments. In conjunction with the study teams, the pathologist contributes an integrated assessment of the significance of study findings ..

Last verified - 1 day(s) 5 hour(s) ago



Director, Rheum/Derm Field Operations & Capabilities
East Hanover, NJ
Novartis provides innovative healthcare solutions that address the evolving needs of patients and societies. Headquartered in Basel, Switzerland, Novartis offers a diversified portfolio to best meet these needs: innovative medicines, cost-saving generic and biosimilar pharmaceuticals and eye care. Novartis has leading positions globally in each of these areas. In 2016, the ..

Last verified - 1 day(s) 4 hour(s) ago



Regulatory CMC Manager/Senior Manager Writer
East Hanover, NJ
The Regulatory CMC Manager/Senior Manager Writer focuses on providing and driving creation of global CMC regulatory documentation for biologic projects/products covering development, registration and approval/post approval activities. Responsibilities: 1. Author/Co-author high-quality CMC regulatory documentation for HA submission, applying CMC global regulatory strategies, assuring technical congruency and regulatory compliance. 2. As early ..

Last verified - 1 day(s) 4 hour(s) ago



Trade Return Goods Coordinator
East Hanover, NJ
The Trade Return Goods Coordinator is responsible for the data entry functions of the Trade Operations group. This position will serve as the primary point of contact for Third Party Logistic Company inquiries pertaining to RA issuance and returned products. This role supports the Trade Analyst and Manager. Major Accountabilities: Responsible ..

Last verified - 1 day(s) 5 hour(s) ago



Clinical Development Medical Director-Ophthalmology
East Hanover, NJ
The Clinical Development Medical Director is the clinical leader of defined program level activities (e.g. submission activities, briefing books etc.), or a large, complex trial, under the leadership of the (Sr.) GPCH. May lead a section of a clinical program (e.g., an indication, a new formulation, or a specific development phase). ..

Last verified - 1 day(s) 5 hour(s) ago


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