Principal Scientist In Vivo Immunology at GSK

Hobart, Tasmania, Australia -

Full Time

Start Date

Immediate

Expiry Date

06 Jul, 26

Salary

0.0

Posted On

07 Apr, 26

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

In vivo immunology, Preclinical study design, Murine studies, Flow cytometry, ELISPOT, Luminex, Meso scale discovery, Animal handling, Drug administration, Necropsy, Tissue harvest, IVIS imaging, Protocol development, Data analysis, Matrix management, Scientific writing

Industry

Pharmaceutical Manufacturing

Description

Site Name: USA - Massachusetts - Cambridge Posted Date: Apr 7 2026 At GSK, we have bold ambitions for patients, aiming to positively impact the health of 2.5 billion people by the end of the decade. Our R&D focuses on discovering and delivering vaccines and medicines, combining our understanding of the immune system with cutting-edge technology to transform people’s lives. GSK fosters a culture ambitious for patients, accountable for impact, and committed to doing the right thing, making sure that we focus our efforts on accelerating significant assets that meet patients’ needs and have the highest probability of success. We’re uniting science, technology, and talent to get ahead of disease together. Find out more: Our approach to R&D Job Purpose: The Principal Scientist in the in vivo immunology team will serve as the preclinical in vivo study lead and will represent the project team in spearheading GSK’s innovation of novel viral vaccines and platform programs. You will have the opportunity to lead the in vivo efforts on multiple viral vaccine programs and platforms within GSK and with external partners in a collaborative and matrix team. You will design and write in vivo study protocols, coordinate and initiate preclinical studies, conduct and analyze experimental results pertaining to the understanding of the immune responses from novel vaccine candidates, formulations, and platforms. Key responsibilities: This role will provide you with the opportunity to lead key activities and to progress your career based on performance. The responsibilities include the following: Design, plan, conduct, coordinate, monitor, and analyze in vivo murine studies for vaccine and platform programs. May serve as the preclinical in vivo lead. Implement and ensure adherence to GSK and regulatory requirements for compliance with Institutional Animal Care and Use Committee (IACUC) guidelines through writing and reviewing in vivo study protocols and participating in the independent scientific review committee. Conduct dosing, In Vivo Imaging System (IVIS) imaging, necropsy, and tissue harvest from animal studies and supervise technicians conducting these activities Perform experiments characterizing cell-mediated immune response for preclinical immunogenicity or challenge studies using flow cytometry, Enzyme‑Linked ImmunoSpot (ELISPOT), Luminex or Meso Scale Discovery (MSD) assays and others. As a preclinical in vivo study lead, you will work in a matrix team to support the identification of novel vaccine candidates and support platform development. Prepare and document study protocols and final reports for projects as an author. Contribute to patent filing, Investigational New Drug (IND) submissions, and scientific publications. Present study plans and results at project meetings. Develop new experimental techniques based on project needs. Mentor and train junior scientists. Basic qualifications Doctor of Philosophy (Ph.D.) or Master of Science (M.S.) degree in immunology or a related field. 4+ years of working experience post Ph. D or 6+ years of working experience post M.S in immunology or in these related field. Experience in conducting in vivo animal studies within the fields of vaccines, infectious diseases, or immunology. Experience in small rodent handling and drug administration, in-study blood sampling, necropsy, tissue harvest, and processing. Experience in designing, executing, and analyzing immune response readouts using conventional or spectral flow cytometry. Preferred qualifications Matrix management experience. A collaborative team player with strong interpersonal skills to work with diverse groups within the organization. Detail-oriented with the agility to balance multiple projects. Extremely organized with experience in documentation of study protocols and reports. Experience with immune-response related readout methods such as ELISPOT, Luminex, and qPCR methodologies. Experience preparing and delivering written and verbal communications in a professional setting. #GSK-LI • If you are based in Cambridge, MA; Waltham, MA; Rockville, MD; or San Francisco, CA, the annual base salary for new hires in this position ranges $115,500 to $192,500. The US salary ranges take into account a number of factors including work location within the US market, the candidate’s skills, experience, education level and the market rate for the role. In addition, this position offers an annual bonus and eligibility to participate in our share based long term incentive program which is dependent on the level of the role. Available benefits include health care and other insurance benefits (for employee and family), retirement benefits, paid holidays, vacation, and paid caregiver/parental and medical leave. If salary ranges are not displayed in the job posting for a specific country, the relevant compensation will be discussed during the recruitment process. Please visit GSK US Benefits Summary to learn more about the comprehensive benefits program GSK offers US employees. Why GSK? Uniting science, technology and talent to get ahead of disease together. GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale. People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people. If you require an accommodation or other assistance to apply for a job at GSK, please contact the appropriate Recruitment Staff by emailing us at - usrecruitment.adjustments@gsk.com GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law. Important notice to Employment businesses/ Agencies GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site. Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK’s compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at https://openpaymentsdata.cms.gov/

Responsibilities

The Principal Scientist will lead preclinical in vivo studies for viral vaccine programs, designing protocols and coordinating experimental execution. They will also analyze immune responses, document findings for regulatory submissions, and mentor junior scientific staff.