MSAT Senior Principal Scientist, Physician Communications

  • Vertex Pharmaceuticals, Inc
  • Boston, Massachusetts
  • Full Time

Job Description

The MSAT Senior Principal Scientist, Physician Communications, will serve as the critical interface between commercial Casgevy manufacturing operations, Manufacturing Science and Technology, internal Commercial teams, and external physician stakeholders. This role will be instrumental in ensuring clear, concise, and accurate communication, in alignment with Vertex-approved content, regarding individual patient outcomes in manufacturing, addressing physician inquiries, and facilitating a collaborative approach to optimize the customer experience .

The ideal candidate will possess a strong scientific and/or clinical background, experience with GMP manufacturing, exceptional communication skills, and the ability to translate complex technical information into easily understandable insights for a diverse audience. This individual will be a key resource in supporting our commitment to patient well-being and product excellence.

Key Duties and Responsibilities

  • Physician Communication: Serve as the primary point of contact for commercial teams in physician communications regarding manufacturing/patient outcomes, including potential deviations, delays, or other issues. Provide timely and transparent updates, answering questions and addressing concerns in a clear, empathetic, and scientifically sound manner.
  • Internal Collaboration & Coordination: Work closely with manufacturing, quality control, quality assurance, and MSAT investigation teams to gather comprehensive information on patient-specific manufacturing runs. Synthesize complex data and technical findings into digestible summaries for physicians and commercial teams. Work with Vertex Legal and Commercial to evolve the agreed/allowed communication content.
  • Issue Resolution & Investigation Support: Partner with scientific teams to understand the root cause investigations of manufacturing anomalies that may impact manufacturing outcomes. Provide physicians with relevant insights into these investigations, without disclosing proprietary information.
  • Cross-Functional Liaison: Facilitate effective communication between commercial teams, manufacturing, and scientific groups to ensure a unified understanding of patient cases and to support commercial strategies with accurate technical information.
  • Documentation & Reporting: Maintain detailed records of physician interactions, inquiries, and manufacturing outcome discussions. Contribute to internal reports summarizing trends in patient outcomes and physician feedback.
  • Training & Education: Potentially assist in developing educational materials or providing training to commercial teams on manufacturing processes and common queries related to patient outcomes.

Required Education Level

  • Advanced degree (Ph.D., MD, PharmD, M.S.) in a relevant scientific or medical discipline (e.g., Cell Biology, Immunology, Biomedical Engineering, Chemical Engineering, Biochemistry).

Required Experience

  • Minimum of 5-7 years of experience in the biopharmaceutical industry, preferably with direct experience in cell and gene therapy, manufacturing, and/or clinical development.
  • Demonstrated experience in a role requiring significant scientific or medical communication with external stakeholders, particularly healthcare professionals.
  • understanding of GxP regulations and manufacturing processes within the biopharmaceutical and ATMP industry.
  • Exceptional written and verbal communication skills, with the ability to explain complex scientific and technical concepts clearly, simply and concisely to non-experts.
  • Proven ability to work collaboratively in a cross-functional team environment.
  • Excellent problem-solving skills and the ability to remain calm and professional under pressure.
  • Strong analytical skills and attention to detail.
  • Ability to travel occasionally, < />

Pay Range:

$164,900 - $247,400

Disclosure Statement:

The range provided is based on what we believe is a reasonable estimate for the base salary pay range for this job at the time of posting. This role is eligible for an annual bonus and annual equity awards. Some roles may also be eligible for overtime pay, in accordance with federal and state requirements. Actual base salary pay will be based on a number of factors, including skills, competencies, experience, and other job-related factors permitted by law.

At Vertex, our Total Rewards offerings also include inclusive market-leading benefits to meet our employees wherever they are in their career, financial, family and wellbeing journey while providing flexibility and resources to support their growth and aspirations. From medical, dental and vision benefits to generous paid time off (including a week-long company shutdown in the Summer and the Winter), educational assistance programs including student loan repayment, a generous commuting subsidy, matching charitable donations, 401(k) and so much more.

Flex Designation:

Hybrid-Eligible Or On-Site Eligible

Flex Eligibility Status:

In this Hybrid-Eligible role, you can choose to be designated as:

  1. Hybrid: work remotely up to two days per week; or select

  2. On-Site: work five days per week on-site with ad hoc flexibility.

Note: The Flex status for this position is subject to Vertex's Policy on Flex @ Vertex Program and may be changed at any time.

Company Information

Vertex is a global biotechnology company that invests in scientific innovation.

Vertex is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, sex, gender identity or expression, age, religion, national origin, ancestry, ethnicity, disability, veteran status, genetic information, sexual orientation, marital status, or any characteristic protected under applicable law. Vertex is an E-Verify Employer in the United States. Vertex will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law.

Any applicant requiring an accommodation in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should make a request to the recruiter or hiring manager, or contact Talent Acquisition at ...

Job ID: 486454571
Originally Posted on: 7/23/2025

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