Full-Time General Manager jobs in the Biotechnology & Pharmaceuticals industry in Andover, Massachusetts

Global Marketing Product Manager/Senior Product Manager, Gaucher Disease This person will play a major role in launching a transformative new therapy within Genzyme's flagship business unit. Part of a small team within one of the world's leading biotechnology companies, this role has immediate visibility, diverse challenges and the opportunity to learn virtually all aspects of the business. Respon...
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. JOB PURPOSE This role is key for assessment of feasibility of clinical trials proposed or to be performed by the Clinical & Sciences Operation Platform (C&SOP) of Sanofi-Aventis R&D. The Feasibility Manager (FM) is the central point of contact for coordination and conduct of the feasibility assessments and provide reliable and consolidated results at the C&SOP level utilising wide sources of dat...
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Senior Manager - Corporate Accounting - CPA International, industry leading, products firm, with billions in revenue, is looking for a a dynamic Assoc Director of Accounting to oversee the accounting of a number of complex areas. This accounting leader will own all issues surrounding these key areas, including month end close, financial analysis, research and implementation of changes as well as a...
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Job Summary: The Controlling Sr. Manager is responsible for leading the day to day activities of the U.S. Genzyme CSO (Clinical Sciences and Operations) Financial Controlling function. This position is primarily responsible for ensuring the accurate recording of financial information with respect to Genzyme CSO cost centers, ongoing CSO client support and ensuring adherence to all related financia...
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Role Summary: The Manager/Sr Manager, Global Services Continuous Improvement will be part of a team that drives process improvement initiatives across the Sanofi Global Services Division (GSD). They will serve as a change agent who leads teams to execute projects using a variety of continuous improvement tools and methodologies. The scope of these initiatives includes key business processes and se...
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Primary Duties: Under the direction of the Director of Regulatory Affairs direct and manage Regulatory Affairs activities for developing and executing CMC strategies across product life cycles. Mange submissions and interactions with the FDA and other regulatory agencies for CMC issues. Provide regulatory support, guidance and expertise to internal groups such as product development, QA, QC and ma...
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Position Summary: Outstanding opportunity to join a fast paced team that is seeking to continuously improve and expand training capabilities for the Sanofi Biosurgery/Device Franchise. Through extensive assessment and collaboration with cross functional stakeholders you will design impactful training plans supporting commercial effectiveness. This position reports to the Director of Commercial Cap...
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Responsibilities: Review the Triage incoming reports for initial assessment of seriousness, expectedness, causality, and reportability for reports from clinical trials and post marking sources in accordance with local work instructions, US FDA regulations, and international guidelines and regulations with high level of accuracy, accountability, and minimal supervision Assist with data entry of inc...
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JOB TITLE: Project Coordinator I BASIC SUMMARY: Assist in the coordination, organization, and prioritize study tables as well as assist in the review of in-life data. This is an entry to mid-level position with the expectations of supervised and/or semi-independent functionality, demonstrating a comfortable level of project coordinating and writing skills in the Medical Writers Department. ESSENTI...
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. Sanofi, a global and diversified healthcare leader, discovers, develops and distributes therapeutic solutions focused on patients' needs. Sanofi has core strengths in the field of healthcare with seven growth platforms: diabetes solutions, human vaccines, innovative drugs, rare diseases, consumer healthcare, emerging markets and animal health. Sanofi is listed in Paris (EURONEXT: SAN) and in New...
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. This role is key for medical supervision and medical management of clinical trials in the North American Region (US & Canada). The Medical Advisor (MA) is the medical link between Medical Operations (and/or Units/Customers) and (potential) investigators or experts/Key Opinion Leaders (KOL's) in North American Region. He/she should be the medical support in the territory for the studies he/she is...
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. Job Responsibilities/Department Description: The Senior Director, Advertising and Promotion will be responsible for directing the regulatory aspects of internal and external communications including advertising and promotional activities for all Genzyme products as well as the recruitment and management of a staff of Regulatory Affairs Ad/Prom professionals. The product portfolio includes multip...
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