Gene Editing Senior Research Fellow, Non-Viral Delivery
Vertex
Country: United States of America
Location: Boston, MA
Time Type: Full time
Posted On: December 13, 2024
Job Description
Gene Editing Senior Research Fellow, Non-Viral Delivery
GENERAL SUMMARY
The Gene Editing Senior Research Fellow, Non-viral Delivery has an impressive history of accomplishments which contribute significantly 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 refined, 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 scientific 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 scientific 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 scientific and ethical development, motivates personnel and resolves conflicts
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 define scientific 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 scientific 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 scientific 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 scientific 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 confidence 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 DesignatedFlex 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