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Senior Research Fellow/Senior Director, Non-Viral Delivery

Vertex Pharmaceuticals Incorporated
United States, Massachusetts, Boston
50 Northern Avenue (Show on map)
Jan 30, 2025

Job Description

Gene Editing Senior Research Fellow, Non-Viral Delivery

GENERAL SUMMARY

The Senior Research Fellow/Senior Director Non-viral Delivery has an impressive history of accomplishments which contribute signicantly to the advancement of projects and is recognized internally and externally as a thought leader in the design, development, and implementation of LNP/VLP non-viral delivery for therapeutic applications. The incumbent applies superior acumen in identifying project needs that are bolstered by rened, systematic creativity and strong judgment of when to launch efforts on a new trajectory. The Gene Editing Senior Research Fellow, Non-viral Delivery will manage the scientic functions and lead the activities of a research group, and may be required to coordinate multiple teams to achieve project goals. The role's responsibilities include the maintenance of organizational balance across teams, as well as setting the scientic directions for personnel. The Gene Editing Senior Research Fellow, optimizes interdisciplinary understanding and synergy within the team and integrates activities with those of other Departments and Project Teams, to help shape cohesive Research plans.

KEY DUTIES and RESPONSIBILITIES

  • Manages activities of the research group across project boundaries

  • Mentors on scientic and ethical development, motivates personnel and resolves conicts

  • Ensures personnel goal setting is effectively linked to corporate and department goals

  • Manages the activities of staff and provides them insightful guidance to succeed and grow

  • Oversees activities of staff and adapts personnel deployment to changing priorities, to ensure key goals of all projects are met on time

  • Helps dene scientic and strategic directions and develops champions of technological innovation for the research group

  • Directs effective, timely and ethical publication and patenting activities for the group

  • Leads effective management of CRO contracts and/or external scientic collaborations

  • Maintains the excellence of standards for structure and interpretation of all laboratory records, electronic database entries, internal reports, patents and external communications from the group.

  • Communicates company objectives to the group and availability of group resources and methods to Project Team(s), in a clear and timely manner, and develops abilities of others in this role

  • Leads preparation of lucid scientic reports for all other branches and levels of the organization and its collaborators, presents expertly when called upon to various stakeholders and senior leadership

  • Responsible for developing and cultivating and high achieving organization

KNOWLEDGE and SKILLS

  • Advanced expertise in state-of-the-art non-viral (e.g. LNP/VLP) delivery technologies for therapeutic applications with a focus on the discovery, development, and implementation of strategies for tissue-specific delivery (expert level)

  • Expertise in the development of cell and/or gene therapies is a plus

  • Demonstrated scientific productivity as evidenced by a strong publication record in top tier journals or equivalent industry accomplishment

  • Highly developed scientic leadership qualities and established prowess integrating the activities of distinct functional groups across multiple projects.

  • Greater aptitude for identifying productive new research initiatives/directions

  • Experienced mentor who effectively infuses condence and team commitment

  • Exhibits a record of excellent operational and ethical standards, and team-improvement

  • Scientifically diverse and effective communicator

  • Possesses greater knowledge of the drug development process and a keener awareness of issues therein

  • Demonstrated success in resolving important organizational problems and/or infusing innovation

EDUCATION and EXPERIENCE

  • Ph.D. (or equivalent degree) in molecular and cell biology, or related disciplines and 10+ years of relevant post-doctoral employment experience.

  • Strong track record of developing non-viral delivery technologies for therapeutic applications.

Flex Designation:

On-Site Designated

Flex Eligibility Status:

In this On-Site designated role, you will 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 ApplicationAssistance@vrtx.com

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