Takeda Development Center Americas, Inc Cambridge, Massachusetts, 02142 Takeda Development Center Americas, Inc. is seeking a Product Manager in Cambridge, MA to drive the development of a product vision, strategy, and global roadmap taking into consideration key stakeholder capability and product needs. Up to 75% telecommuting allowed. Up to 20% domestic and international travel required. Full time. $224,100 - $255,600 per year. Apply on-line at https://jobs.takeda.c |
Pioneer Data Systems Cambridge, Massachusetts, 02139 Our client, a world-leading Pharmaceutical Company in Cambridge, MA is currently looking for a Clinical Data Manager to join their expanding team. Position Details: Job Title: Clinical Data Manager / Digital Health Technology Duration: 12 months contract, extendable up to 36 months Location: Cambridge, MA Note: The client has the right-to-hire you as a permanent employee at any time during or afte |
American Consumer Credit Counselling AUBURNDALE, Massachusetts, 02466 The Business Development Manager will play a pivotal role in expanding ACCC’s reach by developing and managing strategic alliances across various industries. This role is integral to increasing opportunities for credit counseling and debt management services, helping more consumers reduce their debt and become debt-free. Primary Duties and Responsibilities: Strategic Alliances and Partnerships: o |
Takeda Development Center Americas, Inc Lexington, Massachusetts, 02421 Takeda Development Center Americas, Inc. is seeking Senior Manager, Statistical Programming in Lexington, MA to Lead projects directly or indirectly related to GPTs or other functions. Up to 100% remote work allowed from anywhere in the U.S. Full time. $224,000 - $258,000 per year. Apply on-line at https://jobs.takeda.com and search for Req #R0134645. |
Takeda Development Center Americas, Inc Lexington, Massachusetts, 02421 Takeda Development Center Americas, Inc. is seeking a Manager, Global Regulatory Affairs CMC Submissions Management in Lexington, MA to establish global submission activities and timelines in partnership with global and cross-functional stakeholders in Pharmaceutical Science, GMS, Biologics and Small Molecule operating units, Regulatory Affairs, and QA. Up to 20% domestic travel required. Up to 50 |