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FDA Bioassays to Assess NK Cell Functions of Therapeutic mAbs in Tumor Microenvironment Fellowship

Office of Intramural Training & Education
Silver Spring, MD Full Time
POSTED ON 12/22/2024 CLOSED ON 2/21/2025

What are the responsibilities and job description for the FDA Bioassays to Assess NK Cell Functions of Therapeutic mAbs in Tumor Microenvironment Fellowship position at Office of Intramural Training & Education?

About the position

  • Applications will be reviewed on a rolling-basis. FDA Office and Location: A research opportunity is available within the Food and Drug Administration (FDA) in The Center for Drug Evaluation and Research (CDER), located at Silver Spring, Maryland. The Center for Drug Evaluation and Research (CDER) performs an essential public health task by making sure that safe and effective drugs are available to improve the health of people in the United States. As part of the U.S. Food and Drug Administration (FDA), CDER regulates over-the-counter and prescription drugs, including biological therapeutics and generic drugs. This work covers more than just medicines. Research Project: This project will be in the Office of Pharmaceutical Quality Research (OPQR), Office of Pharmaceutical Quality (OPQ). This project will develop and qualify optimal cell-based potency assay(s) for FDA regulated therapeutics that include immune effector cell functions, and to demonstrate that the optimized assay(s) reflect the in vivo mechanism of action of the products either using in vitro cell based assays or tumor microenvironment models. Learning Objectives: Under the guidance of the mentor, the participant will gain knowledge on monoclonal antibody therapies and bioassay development and qualification. The participant will be trained in classical immunology, biochemistry, molecular biology, and cell biology by developing cell-based bioassays. Anticipated Appointment Start Date: 2024/2025. Start date is flexible and will depend on a variety of factors. Appointment Length: The appointment will initially be for nine months, but may be renewed upon recommendation of FDA and is contingent on the availability of funds. Level of Participation: The appointment is full time. Citizenship Requirements: This opportunity is available to U.S. citizens, Lawful Permanent Residents (LPR), and foreign nationals. Non-U.S. citizen applicants should refer to the Guidelines for Non-U.S. Citizens Details page of the program website for information about the valid immigration statuses that are acceptable for program participation. This program, administered by ORAU through its contract with the U.S. Department of Energy to manage the Oak Ridge Institute for Science and Education, was established through an interagency agreement between DOE and FDA. The participant will receive a monthly stipend commensurate with educational level and experience. Proof of health insurance is required for participation in this program. Participants do not become employees of FDA, DOE or the program administrator, and there are no employment-related benefits. Completion of a successful background investigation by the Office of Personnel Management is required for an applicant to be on-boarded at FDA. OPM can complete a background investigation only for individuals, including non-US Citizens, who have resided in the US for a total of three of the past five years. FDA Ethics Requirements If an ORISE Fellow, to include their spouse and minor children, reports what is identified as a Significantly Regulated Organization (SRO) or prohibited investment fund financial interest in any amount, or a relationship with an SRO, except for spousal employment with an SRO, and the individual will not voluntarily divest the financial interest or terminate the relationship, then the individual is not placed at FDA. For additional requirements, see FDA Ethics for Nonemployee Scientists. FDA requires ORISE participants to read and sign their FDA Education and Training Agreement within 30 days of his/her start date, setting forth the conditions and expectations for his/her educational appointment at the agency. This agreement covers such topics as the following: Non-employee nature of the ORISE appointment; Prohibition on ORISE Fellows performing inherently governmental functions; Obligation of ORISE Fellows to convey all necessary rights to the FDA regarding intellectual property conceived or first reduced to practice during their fellowship; The fact that research materials and laboratory notebooks are the property of the FDA; ORISE fellow’s obligation to protect and not to further disclose or use non-public information.

Apply for this vacancy

What you'll need to apply

A complete application consists of:

An application Transcripts –
  • A current resume/CV, including academic history, employment history, relevant experiences, and publication list
  • One educational or professional recommendation

All documents must be in English or include an official English translation.

Contact name

Mentor

Contact email

ORISE.FDA.CDER@orau.org

Qualifications

The qualified candidate should be currently pursuing or have received a doctoral degree in the one of the relevant fields. Preferred skills: Experience in assay development is favorable.

Disclaimer/Fine Print

The application must be completed through Zintellect.

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