Partners with the US Pain VP & BU Leadership Team to proactively shape the launch plan, and autonomously manages launch activity tracking and launch readiness team Drives the development high impact executive, cross functional and cross team presentations and communications, including executive presentations, business reviews, and department town halls Manages the annual

The Director, GCP Compliance is responsible for the escalation and management and compliance activities in support Quality Issues Management and other activities within RDQA. This role will act as a lead for GCP related events and escalation of these events. This individual will work closely with Quality Leads, Study team members, and other pillars in the Quality organiza

Establishes meaningful and professional relationships within key accounts across multiple layers of the hospital system (key hospital medical and administrative staff, pharmacies, formulary decision makers and KTLs) Develops and maintains expertise on the product's clinical attributes and patient unmet need and educates healthcare professionals on product use in appropria

Reporting to the Director of Inspection Excellence within Clinical Quality Management, the Clinical Quality Management Associate Director will support the management and operational oversight of Quality Events and is responsible for leading Quality Event Management activities for Global Clinical Operations (GCO) assigned unplanned deviations, corrective/ preventive action

The Technical Accounting and SEC Reporting Associate Director is primarily responsible for researching and documenting accounting positions and analyses for a variety of complex areas, as well as proactively monitoring and performing impact analyses with respect to new accounting standards and other regulatory developments. This position is based in our Boston, MA office,

This role will report to the senior manager of Product Development and focus on the design and transfer of implantable cell encapsulation devices for delivering proprietary cells. The successful candidate will join the Process Engineering Team and work closely with Research and Development, Device Quality Control, Device Quality Assurance, Regulatory Affairs, and Manufact

Appropriately partners with internal stakeholders across functions (Payer Accounts, State Government Affairs, Hospital Account Managers, Marketing, Patient Support) to develop and achieve targeted plans of action. Collaborates closely with Field Payer teams on coverage policy developments and coding education Develops and maintains geographic and account business plans Es

The Senior Principal Research Scientist is self reliant with a proven record of accomplishments, independently identifying and solving complex problems using sophisticated scientific methods and analytical thought, across a number of critical and diverse projects. The Senior Principal Research Scientist encourages use of diverse experimental approaches within their area o

Maintain a high level of productivity in the laboratory setting Develops and executes clear synthetic routes using state of the art synthetic methodologies Primarily responsible for executing organic syntheses in a timely, efficient, and independent manner Create and interpret SAR with a clear understanding of the biological data Organize and triage efforts to stay consis

Lead the delivery of therapeutic area specific analytical insights in response to market access landscape, issues and trends. Generate insights and develop KPIs as part of US market access readiness launch activities, including evaluating in market analogs pricing & contracting environment, payer/PBM landscape, clinic/hospital economics, employer groups, value based agree

The Associate Director (AD), Commercial Supply Chain Risk Management will aid in formulating and executing, optimizing, stabilizing, and scaling of the new Risk Management framework and overall Risk Management strategy to ensure it keeps pace with the growth of the company and Commercial Manufacturing and Supply Chain (CMSC). The Associate director will also play a role i

Oversee material requirements and lead the device raw material planning process for the providence, RI site for BOM and non BOM materials. Partner with CMC, Procurement and Strategic Sourcing to ensure supply and solve supplier and materials related issues. Manage direct and indirect materials for manufacturing activities, as well as materials for packaging/labeling and s

Independently authors routine and complex clinical and regulatory documents Provides strategic input into program level plans Deep insight into how different functions contribute to the successes of the team Aligns, coordinates, and builds consistent information and messages across clinical program(s) Provides leadership related to the activities of Medical Writing Scienc

The Vendor Quality Management Director provides technical and strategic leadership for vendor quality, vendor quality processes, and associated governance for the cell and gene therapy business unit. This position focuses not just on the "what" but the "how", ensuring phase appropriate and risk based compliance. This is a hybrid role located in our Seaport offices. Key Du

Function as the first/primary point of contact for all Vertex interests/activities at certain ATMP cell and gene therapy Contract Development and Manufacturing Organizations (CDMOs) Provide operational oversight of, and troubleshooting support to, CDMOs to ensure all deliverables meet or exceed Vertex requirements (including but not limited to successful execution of manu