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Regulatory Affairs Specialist

Department of Health and Human Services
National Institutes of Health
The National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
This job announcement has closed

Summary

This position is located in the National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK), Office of the Director (OD), Office of Clinical Research Support (OCRS). As a Regulatory Affairs Specialist, you will collaborate with the Office of Clinical Research Support, Program Officers and extramural offices, as well as serve as an expert advisor to leadership in order to establish and maintain regulatory best practices and implement project procedures.

Overview

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Hiring complete
Open & closing dates
06/03/2024 to 06/07/2024
Salary
$117,962 to - $153,354 per year
Pay scale & grade
GS 13
Location
1 vacancy in the following location:
Montgomery County, MD
Remote job
No
Telework eligible
Yes—as determined by the agency policy.
Travel Required
Not required
Relocation expenses reimbursed
No
Appointment type
Permanent
Work schedule
Full-time
Service
Competitive
Promotion potential
13
Job family (Series)
Supervisory status
No
Security clearance
Other
Drug test
No
Position sensitivity and risk
Moderate Risk (MR)
Trust determination process
Announcement number
NIH-NIDDK-DE-12410037
Control number
793350700

This job is open to

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Clarification from the agency

You must be a U.S. Citizen or U.S. National. Foreign nationals or legal permanent residents are not eligible for consideration. This job is also open to USPHS Commissioned Corps Officers and Call-To-Active Duty (CAD) Candidates.

Duties

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As a Regulatory Affairs Specialist your duties will include but are not limited to the following:

  • Serve as a sponsor for regulatory applications submitted to the Food & Drug Administration (FDA) for NIDDK extramural clinical trials as well as intramural studies conducted within the NIH/NIDDK clinical laboratories.
  • Analyze, Develop and Standardize policies, procedures, and guidelines for Standard Operating Procedures (SOPs) for Investigational New Drug (IND) and Investigational Device Exemption (IDE) applications, international drug regulatory policies, SAE identification and reporting.
  • Serve as a the senior regulatory specialist and expert advisor to NIDDK leadership.
  • Work with study teams to devise or advise on strategies to engage/collaborate with FDA on more challenging or higher risk protocols under IND/IDE.
  • Monitor and provide guidance on regulatory activities.
  • Manage IND and IDE activities and facilitate communications internally and externally.
  • Ensure incoming and historical documents from FDA regulated studies are filed appropriately and the Investigator and Sponsor regulatory record is complete and in compliance with FDA regulations, guidance, policies and procedures.
  • Establish standards for clinical site monitoring, essential regulatory document reviews and protocol activity tracking.

Requirements

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Conditions of employment

  • U.S. Citizenship requirement or proof of being a U.S. National must be met by closing date.
  • Employment is subject to the successful completion of a background investigation, verification of qualifications, completion of onboarding forms, submission of required documents, and any other job-related requirement before or after appointment.
  • Applicants must meet all qualification requirements by the closing date of this announcement.
  • Males born after December 31, 1959 must be registered with the Selective Service.
  • Position has an education requirement (please include transcripts).

Qualifications

In order to meet the Basic Qualification Requirements for a Regulatory Affairs Specialist, GS-0601-13, you must:

  • Have a Bachelor's or higher-level degree from an accredited university with a major study in an academic field related to the medical field, health sciences or allied sciences appropriate to the work of this position.
AND

In addition to the basic education requirements, you must demonstrate in your resume at least one (1) year of qualifying experience equivalent to at least the GS-12 level in the Federal service obtained in either the private or public sector, performing the following types of tasks: providing expert regulatory guidance to investigators, team members, and pharmaceutical partners, including technical expertise, on the development of Investigational New Drug (IND) and Investigational Device Exemption (IDE) applications and requests; preparing meeting requests and briefing documents and advising investigators on regulatory compliance; providing writing guidance for internal inspections; evaluating study documents and safety report cases for validity and consistency; and developing and maintaining liaison for site performance and compliance issues.

You will receive credit for all experience material to the position, including experience gained in religious, civic, welfare, service, and organizational activities, regardless of whether you received pay.

Do not copy and paste the duties, specialized experience, or occupational assessment questionnaire from this announcement into your resume as that will not be considered a demonstration of your qualifications for this position.

Preview assessment questionnaire before you apply: https://apply.usastaffing.gov/ViewQuestionnaire/12410037

Education

This position has an education requirement. You are strongly encouraged to submit a copy of your transcripts (or a list of your courses including titles, credit hours completed and grades). Unofficial transcripts will be accepted in the application package. Official transcripts will be required from all selectees prior to receiving an official offer. Click here for information on Foreign Education.

Additional information

  • This position is designated as a Tier II "non-emergency/teleworker" position and the selected candidate will be considered a "non-emergency/teleworker" employee. In the event of a closure, you must be available to telework or request leave.
  • A one-year probationary period may be required upon selection/placement.
  • At the supervisor's discretion, this position may offer work schedule flexibilities: [telework (work from home on a regular basis or ad hoc basis but reports to the office at least once a week/two days a pay period), compressed schedules].
  • PHS Commissioned Officers interested in performing the duties of this position within the Commissioned Corps should apply online to this announcement to receive consideration
  • We may make additional selections for similar positions within the commuting area(s) of the locations listed through this vacancy announcement. By applying, you agree to have your application shared with any interested selecting official(s). Clearance of CTAP/ICTAP will be applied for similar positions.
  • The National Institutes of Health participates in the USCIS Electronic Employment Eligibility Verification Program (E-Verify). E-Verify helps employers determine employment eligibility of new hires and the validity of their Social Security numbers.
  • The NIH maintains a tobacco free work environment and campus.
  • Must be able to perform the essential duties of the position, with or without reasonable accommodation.
  • Visit our Applicant FAQs page for helpful information on the application process.
  • Visit our Total Compensation page and this sample for a detailed look into the benefits, awards, leave, retirement, and other incentives employees may receive as part of a rewarding work environment.

How you will be evaluated

You will be evaluated for this job based on how well you meet the qualifications above.

You will be assessed on the following competencies (knowledge, skills, abilities, and other characteristics):

  • 1. Ability to provide regulatory guidance on the development of Investigational New Drug and Investigational Device Exemption applications and requests.
  • 2. Ability to provide safety oversight for clinical trials.
  • 3. Skill in preparing reports and documentation on clinical trials and regulatory applications.
  • 4. Skill in providing operational support for clinical trials.


If you meet the minimum qualifications for this position, your application and responses to the online questionnaire will be evaluated under Category Rating and selection procedures for placement in one of the following categories:
  • Best Qualified - for those who are superior in the evaluation criteria
  • Well Qualified - for those who excel in the evaluation criteria
  • Qualified - for those who only meet the minimum qualification requirements
The Category Rating Process does not add veterans' preference points but protects the rights of veterans by placing them ahead of non-preference eligibles within each category. Applicants determined to be Best Qualified will be referred for further consideration. Preference eligibles in the Best Qualified category are referred before all other applicants.

To determine your qualifications and referral status, we may review your resume and supporting documentation and compare it against your responses to the vacancy questionnaire. Ensure you support your self-ratings by the information you provide in your application. We may verify or assess your qualifications at any time. Inflated or unsupported qualifications may affect your rating. Any misrepresentation or material omission of facts may be sufficient cause to end further consideration of your candidacy. Persons listed as having knowledge of your past accomplishments or experience in your application may be contacted for verification purposes at any time. Verification may, but need not, begin prior to receiving an offer.

To be considered well qualified for the purposes of the Career Transition Assistance Program (CTAP) and the Interagency Career Transition Assistance Program (ICTAP), you must be able to satisfactorily perform the duties of the position upon entry and substantively exceed the basic qualifications by scoring at least an 85 on the assessment and meet all eligibility, physical, medical, suitability, and all other requirements.

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