Senior Scientist, Discovery- Oncology In Vivo
About the role
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advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
About Oncology
Role Overview
Key Responsibilities
Design, execute, and interpret
Develop and optimize
Lead
Perform and oversee
Analyze and present
Collaborate
Manage multiple projects simultaneously
Mentor and supervise
Contribute to ex vivo analyses
Stay current
Communicate clearly and professionally
Flexibility required
Qualifications
- Bachelor's degree (BS/ BA) in the life sciences (molecular/ cellular biology, biochemistry, pharmacology, tumor immunology) with at least 10 years of relevant pharmaceutical or biotech industry/ lab/ academic experience OR a Master's degree (MS) with at least 7 years of relevant experience, or PhD with 1-3 years of relevant post-graduate experience.
- Ability to cell culture of cancer and immune cells.
- Experience with oncology-relevant xenografts and syngeneic mouse models is required; primary grafts, orthotopic models, humanized models, or genetically engineered tumor models are preferred.
- Experience with small molecules and/ or biologics is required
- Experience with immune-modulatory agents, vaccines or cell therapies such as CAR-Ts is desirable.
- Strong skills in tumor implantation techniques and dosing, proper handling of therapeutics, tumor measurement, health monitoring, and data collection and analysis are required.
- Experience with bioluminescent imaging, flow cytometry, IHC, ELISA, RT-PCR, Westerns, or Luminex® is desirable.
- Strong organizational skills including the ability to manage several projects simultaneously; detail oriented with excellent record keeping skills are required.
- Excellent interpersonal skills with the ability to interact effectively with matrixed teams, internally and externally, is required.
- Excellent data management and record-keeping skills are required.
- Ability to effectively present scientific data and concepts to colleagues and teams is critical, and experience presenting at external meetings is also required.
- Proven track record of adherence to animal welfare and compliance regulations is critical.
- Experience with mentoring or managing direct reports is desirable.
- Experience in writing technical drafts for patent filings, IND (US-FDA) or CTA (EMA) filings is desirable.
Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.
Johnson & Johnson is committed to providing an interview process that is inclusive of our applicants' needs. If you are an individual with a disability and would like to request an accommodation, external applicants please contact us via https://www.jnj.com/contact-us/careers , internal employees contact AskGS to be directed to your accommodation resource.
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Preferred Skills
Not included in the source posting: benefits.
Skills
Who can apply
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