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Preclinical Safety Assessment (PSA) is a global function responsible for the design and conduct of nonclinical safety programs for the comprehensive safety assessment of Vertex therapies at all stages of discovery and development. Vertex Pharmaceuticals uses cutting edge science and technologies to perform robust assessments of novel...

Job DescriptionGENERAL POSITION SUMMARY: The Manager, Global Medical Communications will be responsible for brand or Cystic Fibrosis disease specific global medical communication strategies and execution of those plans for designated brands at Vertex.

The Manager, Global Patient Safety (GPS) Individual Case Safety Report (ICSR) is responsible for performing triage of all safety information, providing vendor management and oversight of ICSR processing activities, and has operational and line management responsibility of the Intake team.

Vertex Pharmaceuticals creates new possibilities in medicine to cure diseases and improve people’s lives. The Associate Director, Drug Product Tech Transfer/Commercial Manufacturing is responsible for the successful tech transfer, validation, and commercial manufacturing of drug product in an innovative, high-science, Quality-by-Design,...

GENERAL POSITION SUMMARY:The primary responsibility of the Associate Director, Global Medical Communication, Triple Combination will oversee the execution of the brand specific medical communication plan in collaboration with the Director, Triple Combination Medical Communications and Lead Medical Director.

Job DescriptionGENERAL POSITION SUMMARY: The primary responsibility of the Associate Director, Global Medical Communication, Triple Combination will oversee the execution of the brand specific medical communication plan in collaboration with the Director, Triple Combination Medical Communications and Lead Medical Director.

Job DescriptionThe Director, Early Career Talent Acquisition will be responsible for developing and executing the strategy for attracting and recruiting students and early career talent. A key part of this role will be to develop and implement a university relations strategy at specific target campuses.

The Associate Director Clinical Outsourcing provides leadership to the clinical research Outsourcing managers within the Outsourcing function. Responsibilities include: conception and direction of strategic outsourcing initiatives, utilizing metrics to monitor risk and develop mitigation strategies in outsourced programs, and assurance...

We seek a highly motivated and innovative scientist with extensive biomolecular NMR experience and a passion to apply biophysical techniques to drug discovery The ideal candidate • Will have a proven track record in NMR structure determination • Provide broad expertise in biophysics, protein biochemistry, and structural biology •...

The Senior Project Manager, Outsourced Programs, possesses proven experience successfully managing and executing projects related to CMC (Chemistry, Manufacturing and Controls) activities, capital improvements, process excellence, supply chain or technical transfer of manufacturing processes.

The Sr Pharmacovigilance Scientist/Medical Writer provides functional area and operational expertise of assigned developmental and/or marketed product(s). He/She collaborates closely with the safety physician and cross-functional partners to evaluate and actively manage risks in accordance with global regulatory frameworks, write...

Vertex Pharmaceuticals is seeking a highly motivated, collaborative histopathology research scientist to join the Preclinical Safety Assessment (PSA) department located at our Boston facility. PSA is a global function responsible for the design and conduct of comprehensive nonclinical safety programs and through its Pathobiology team...

The Senior Director is responsible for overseeing the development and implementation of global regulatory CMC strategies for all large molecule and gene therapy product development. The Senior Director will provide regulatory CMC leadership across projects, teams and committees and will provide strategic and operational leadership...

Biosample Operations Lead Vertex Pharmaceuticals is seeking to recruit a Biosample Operations Lead in support of the company’s clinical research in rare diseases. Responsibilities: • Accountable for planning, coordinating, and overseeing all operational activities required to manage the lifecycle of biomarker samples (oversight of...

Job DescriptionModeling & Simulation (M&S) methodologies plays an increasingly important role in the development of new drugs within Vertex Pharmaceuticals. We are seeking an Associate Director, Modeling & Simulations to add to our Modeling & Simulations group.

Vertex Pharmaceuticals is seeking a toxicologist with expertise in knowledge management and data sciences to join its Predictive and Investigative Safety Assessment team in Boston, MA. Predictive and Investigative Safety Assessment is a global function within the Preclinical Safety Assessment (PSA) department responsible for the design...

The Senior Director, Global Trade, Logistics and Systems will support Vertex’s clinical and commercial programs by ensuring uninterrupted product movement across Vertex’s global drug supply network. In addition, this individual will provide leadership in the development of manufacturing information systems roadmap and aligning that...

This role provides testing support for Release and Stability Laboratory (RSL) department supporting validation, testing and reporting of in-process, release and stability samples. Specific assigned persons are responsible to ensure activities occur in an efficient and cGMP compliant manner while fostering the Vertex vision and values.

We are seeking a creative scientist to join the Global Computational Chemistry group at Vertex and contribute to chemical reaction informatics. The successful candidate will address data analysis, visualization and decision support needs for high throughput reaction screening and synthesis planning.

The Senior Manager is responsible for support and quality oversight for the assigned programs focused on Gene Therapy/ Biologics and possesses a strong knowledge of GCP study oversight and management of quality activities related to clinical trial execution and GMP cell-based production (drug development).