Pediatrics Hematology/Oncology - Project Scientist series - Nowicki Lab

University of California, Los Angeles

$90K — $120K *
Healthcare
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Ph.D. or equivalent qualification
  • Prior experience in clinical research
  • Familiarity with Good Manufacturing Practice (GMP) guidelines
  • Expertise in DNA, RNA and protein isolation and purification
  • Proficient in cell culture techniques, including hematopoietic progenitor cells

Responsibilities

  • Manufacture clinical research products adhering to GMP guidelines
  • Maintain comprehensive records and documents in a GMP environment
  • Conduct post-manufacturing lot-release tests such as Elisa and Mycoplasma assay
  • Support FDA IND applications through experimental design and execution
  • Collaborate on NYESO-TCR research projects using multiparametric flow cytometry

Benefits

  • Access to academic ranking based on experience
  • Opportunities for professional development through seminars and workshops
  • Collaborative working environment within the Division of Hematology-Oncology
  • Engagement in cutting-edge research with potential impact on pediatric medicine
Full Job Description
Position description

The Division of Hematology-Oncology in the Department of Pediatrics of the David Geffen School of Medicine at UCLA is seeking a Project Scientist. The appointment will be in the Project Scientist series; academic rank will be commensurate with experience.

The position requires a Ph.D. or equivalent and prior experience. This is a non-senate position.

Duties and Responsibilities include:
  • Manufacturing products for clinical research according to Good Manufacturing Practice (GMP) guidelines
  • Operate in a GMP regulated environment according current standard operating protocols
  • Meticulous record keeping and maintenance of GMP, GTP and basic research related records and documents.
  • Attend and arrange seminars, training sessions and workshops to maintain competency in evolving current GMP/GTP regulations
  • Performing post-manufacturing lot-release tests: Elisa, Colony-forming Unit (CFU) assay, ELISA, Endotoxin assay, Mycoplasma assay, vector copy number (VCN) test by ddPCR
  • Culture of hematopoietic progenitor cells for in vitro differentiation into T-cells for proof of principle testing of gene delivery
  • Conduct experiments for FDA IND application(s)
  • Conduct DNA, RNA and protein isolation and purification according current GLP research grade protocols
  • Quantification of nucleic acids and proteins
  • Perform PCR and qPCR
  • Perform multiparametric flow cytometry to assist on-going specific NYESO-TCR research project for intracellular, surface and peptide target markers.
  • Culture adhered and non-adherent mammalian cells, preparing media, aliquots and other compounds utilized in tissue culture with proper sterile aseptic technique.
  • Ability to set up co-cultures for killing-assays or peptide release production-analysis
  • Ability to set up experiments utilizing real time in vitro cell imaging system Incucyte
  • Perform ELISA experiments in either cellular supernatants or cellular lysates normalizing results against total protein content
  • Plasmid preparation, bacteria growth on competent E. coli or Stable 3 systems, positive transformants selection and sequences analysis
  • Ability of align sequences on APE-software (or-equivalent) and design plasmids for plasmid-vector construction and PCR analysis
  • Perform plasmid sequencing and re-sequencing
  • Production of high-titer viral vectors, purification and concentration of viral supernatants for retrovirus
  • Production of high-titer viral vectors, purification and concentration of viral supernatants for lentivirus
  • Determination of viral titer by ddPCR on fresh and frozen supernatants
  • Document results of experiments and elaboration of reports for NYESO-TCR team leader
  • Perform experiments associated to survival tittering and transduction efficiency on target cells
  • Design and re-design of viral vectors for large scale manufacture of GMP and GMP-comparable clinical grade virus.
  • Performs other job-related duties as assigned

Interested candidates can apply online at: https://recruit.apo.ucla.edu/JPF10807

UC Regents Statement on Ethical Values and Standards of Conduct:
All aspects of searches are confidential and all candidates are expected to review and abide by UC Regents Policy 1111 on Statement on Ethical Values and Standards of Conduct https://regents.universityofcalifornia.edu/governance/policies/1111.html

Cultural North Star:
The shared values of the DGSOM are expressed in the Cultural North Star, which was developed by members of our community and affirms our unswerving commitment to doing what's right, making things better, and being kind. These are the standards to which we hold ourselves, and one another. Please read more about this important DGSOM program at https://medschool.ucla.edu/cultural-north-star .

Qualifications

Basic qualifications
Ph.D. or equivalent and prior experience

Application Requirements

Document requirements
  • Curriculum Vitae - Your most recently updated C.V.
  • Cover Letter/Personal Statement
  • Statement of Research (Optional)
  • Statement of Teaching (Optional)


Reference requirements
  • 3-5 letters of reference required

Letters to be used as part of the appointment dossier of the selected finalist
Apply link: https://recruit.apo.ucla.edu/JPF10807

Help contact: [email protected]

About UCLA

As a University employee, you will be required to comply with all applicable University policies and/or collective bargaining agreements, as may be amended from time to time. Federal, state, or local government directives may impose additional requirements.

The University of California is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, age, protected veteran status, or other protected status under state or federal law.

As a condition of employment, the finalist will be required to disclose if they are subject to any final administrative or judicial decisions within the last seven years determining that they committed any misconduct.
  • "Misconduct" means any violation of the policies or laws governing conduct at the applicant's previous place of employment, including, but not limited to, violations of policies or laws prohibiting sexual harassment, sexual assault, or other forms of harassment, discrimination, dishonesty, or unethical conduct, as defined by the employer.
  • UC Sexual Violence and Sexual Harassment Policy
  • UC Anti-Discrimination Policy for Employees, Students and Third Parties
  • APM - 035: Affirmative Action and Nondiscrimination in Employment


Job location

Los Angeles, CA

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