Most Recent Ironwood Pharmaceuticals, Inc. Job Listings

This position requires a highly motivated, detail and service orientated individual to be responsible for managing the worldwide collaboration accounting at Ironwood. The Company's lead product was approved for marketing in the US and Europe in 2012. The product is being commercialized in the US by Ironwood and its collaboration partner, Forest Laboratories, and the parties share e...

We are seeking aCompliance Analyst/Manager toaudit and monitor key business activities as part of our Corporate Compliance program, including monitoring and assessment of activities pertaining to (1) pharmaceutical product promotion; (2) medical affairs interactions; (3) clinical research and development, (4) foreign corrupt practices/anti-bribery compliance and (5) adherence to federal and...

We are seeking an experienced Marketing Communications professional to lead the advancement of Ironwood Customer Communications capabilities with physicians and patients. This individual will play a key role in enhancing the ability of Ironwood brand teams to excel in integrated channel marketing and measurement, and will develop, implement and optimize new communication capabilities, techn...

The Director of Enterprise Architecture (EA) is responsible for leading the program to develop, maintain and leverage the enterprise architecture (EA) across the Ironwood organization. Responsible for defining EA governance and processes and leading their integration with related business and IT processes. This position will work closely with IT organization to align future business drivers...

Ironwood recognizes that clinical outcome assessments are critical for achieving product regulatory approvals, creating robust and differentiated product profiles, informing health economic assessments, and providing important information to patients and health care professionals for therapeutic decision-making. The Associate Director will be responsible for supporting the development of cl...

Reporting to Leadership in the Pharmaceutical Development department, the Packaging and Materials Manager is responsible for the packaging, labeling, and distribution of clinical supplies for Ironwood Pharmaceutical's clinical development programs. The position will operate within a collaborative cross-functional team with Quality Assurance, Clinical Operations, Regulatory Affairs, Global O...

This position has the overall responsibility for financial statements and analysis in a deadline-driven, fast-paced accounting organization. This position reports to the Assistant Controller and will have one direct report. Responsibilities - Responsibilities include the following though they may change based on the continuing growth of the Company: Prepare and a...

Business Partner to commercial team and other entities within Ironwood in the delivery and measurement of one-to-many, one-to segment and one-to-one communications to patients and professionals across multiple channels (i.e., direct mail, email, web, mobile, broadcast, etc.). This individual is the owner of the technical service that delivers the ability to set up, deploy, and measure all m...

Ironwood Pharmaceuticals is looking for a highly motivated scientist to join the Pharmaceutical Development group. The successful candidate will perform analytical tests and method development under supervision of a senior level scientist, collaborate with formulation scientists, process chemists and other analytical chemists in a team environment for project support and general lab operati...

Ironwood recognizes that clinical outcome assessments are critical for achieving product regulatory approvals, creating robust and differentiated product profiles, informing health economic assessments, and providing important information to patients and health care professionals for therapeutic decision-making. The Head of Outcome Measurement Study Endpoints will be responsible for leading...

Reporting to the Vice President, Regulatory Affairs, the Director of CMC Regulatory Affairs will be responsible for developing and implementing CMC regulatory strategies as well as coordinating all aspects of CMC regulatory submissions. This person will represent the function of CMC regulatory on project teams within Ironwood as well as serve as the regulatory CMC liaison with partners on d...

Reportingto the Vice President, Regulatory Affairs, the Director of Regulatory Affairs is responsible for developing the overall regulatory strategy for NCE (new chemical entity) development programs in assigned therapeutic area, assuring that regulatory documents are in compliance with health authority regulations and interacting with US and international health authorities.