• Principal Scientist Jobs in United States Of America - 23739115

  • Pfizer Inc.
  • United States Of America, Usa
  • Save Job
  • 5 - 8 Years
  • Posted : above 1 month

Job Description:

ROLE SUMMARY

We seek an accomplished Principal Scientist level oncology/immune oncology scientist to join the in vivo pharmacology group within Oncology Research & Development (ORD) in La Jolla, California The successful candidate will join a dynamic team of scientists in the Oncology In Vivo Pharmacology Group, playing a leading role in guiding project teams in the appropriate planning and use of models of cancer to evaluate new drug candidates, mechanisms and targets

The Principal Scientist/In Vivo Lead will participate in pre-clinical drug discovery and development projects with a focus on immuno-oncology while also contributing to projects related to signal transduction, targeted therapeutics, and epigenetics The successful candidate will be responsible for working with project teams to design, plan and execute an in vivo strategy to ensure efficient and effective project decision-making They will also be a key contributor to the In Vivo Committee, responsible for presenting study plans and obtaining peer input for protocol finalization and approval to meet research project objectives The individual will directly supervise laboratory staff that make up an in vivo team responsible for study performance and data analysis and play a role in the Pharmacology Department strategy The Principal Scientist will provide technical and scientific expertise in in vivo pharmacology across ORD to enable target identification, validation, prioritization and efficient drug discovery Ideal applicants will possess excellent communication, leadership and organizational skills, critical problem-solving abilities, and a commitment to excellence

Establish scientific in vivo strategy and study plans for drug discovery projects
Serve as the in vivo pharmacology lead for several drug discovery projects
Works within multi-functional teams to support target identification, validation, drug discovery and combination therapy
Works across In vivo teams in a highly collaborative manner, sharing expertise and resources to meet study needs across In Vivo Pharmacology
Design and conduct in vivo studies to evaluate and establish efficacy, PK/PD relationship, combination strategy, biomarker identification and analysis
Develop and characterize new in vivo mouse models, including syngeneic tumor and genetically engineered mouse (GEM) models, to study biologic mechanisms and support exploration of novel cancer immune therapeutics and targeted Interpretation, presentation and documentation of experiments as well as preparation of reports
The Principal Scientist will generate and be accountable for the necessary Animal Use Protocols that ensures team members comply with all regulatory requirements and internal policies

Facilitate and lead the development and execution of ancillary in vitro assays necessary to maximize value of the contribution by the in vivo team
Responsible for contribution to relevant in vivo sections of study reports and regulatory documents ie IND filingsWritten and verbal presentation of results within a multidisciplinary team environment Ensure that projects have all critical in vivo data to enable project stage dependent decisionsPublication of results in scientific peer-reviewed journals and presentations at internal, national, and international meetings

BASIC QUALIFICATIONS

PhD in Cancer Biology, Immunology, Biochemistry, Genetics or equivalent experience in a related discipline with > 5 years industry experience with technical and scientific experience in drug discovery and preclinical development
Experience in collaborative research in Oncology drug discovery programs
Expertise in animal models of human cancers as well as strong publication record or evidence of equivalent achievements in industry are desired
Expertise with GEMM and humanized models highly desirableHands on in vivo (eg IV, PO dosing, blood/tissue collection)and ex vivo skills (flow cytometry, western blot, ELISA)
Excellent written and oral communication and presentation skills in English Proficiency in all common office and scientific software

PREFERRED QUALIFICATIONS

Supervisory experience is a significant plus

Sunshine Act

Pfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations These laws and regulations require Pfizer to provide government agencies with information such as a health care providers name, address and the type of payments or other value received, generally for public disclosure Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act Therefore, if you are a licensed physician who incurs recruiting expenses as a result of interviewing with Pfizer that we pay or reimburse, your name, address and the amount of payments made currently will be reported to the government If you have questions regarding this matter, please do not hesitate to contact your Talent Acquisition representative

EEO & Employment Eligibility

Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA Pfizer is an E-Verify employer

Other Job Details

Eligible for Relocation Package
Eligible for Employee Referral Bonus
#LI-PFE

N (Other) (United States of America)

Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates

Profile Summary:

Employment Type : Full Time
Eligibility : Any Graduate
Industry : Biotechnology/Pharmaceutical/Medicine, Manufacturing/Industrial
Functional Area : Bio Tech/R&D/Scientist
Role : Bio-Technology Research
Salary : As per Industry Standards
Deadline : 31st Mar 2020

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