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Supervisory Regulatory and Clinical Operations Specialist

Department of Health and Human Services
National Institutes of Health
National Cancer Institute
This job announcement has closed

Summary

This position is located in the Office of Sponsor and Regulatory Oversight (OSRO), Office of Clinical Director (OCD), Center for Cancer Research (CCR), National Cancer Institute (NCI), National Institutes of Health (NIH), Department of Health and Human Services (HHS).

Overview

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Hiring complete
Open & closing dates
07/25/2024 to 07/29/2024
Salary
$163,964 to - $191,900 per year
Pay scale & grade
GS 15
Locations
1 vacancy in the following locations:
Frederick County, MD
Montgomery County, MD
Remote job
No
Telework eligible
Yes—as determined by the agency policy.
Travel Required
Not required
Relocation expenses reimbursed
Yes—You may qualify for reimbursement of relocation expenses in accordance with agency policy.
Appointment type
Permanent
Work schedule
Full-time
Service
Competitive
Promotion potential
15
Job family (Series)
Supervisory status
Yes
Security clearance
Other
Drug test
No
Position sensitivity and risk
Non-sensitive (NS)/Low Risk
Trust determination process
Announcement number
NIH-NCI-MP-24-12484227
Control number
800510100

This job is open to

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Clarification from the agency

You must be a current or former federal employee eligible to apply under merit promotion procedures or otherwise be eligible as a status applicant (e.g. Veterans Employment Opportunity Act) OR be an individual who is eligible through an OPM interchange agreement or for a non-competitive appointment. This job is also open to USPHS Commissioned Corps Officers and Call-To-Active Duty (CAD) Candidates.

Duties

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  • Managing all Sponsor clinical operations obligations as listed in ICH GCP E6 section 5.
  • Managing all Sponsor activities for sites assessment, initiation, activation and close out.
  • Developing SOPs and processes in support of those actives.
  • Serve a supervisor for the clinical operation team and serve as the COR or COR representative for support contract.
  • Providing expert guidance to investigators, team members, and pharmaceutical partners, on clinical operations to support clinical trials in new and commercial drugs and devices used in the treatment of cancer.
  • Providing expert guidance to investigators, team members, and pharmaceutical partners to ensure IND/IDE study protocols, reports, and documentation conform to applicable guidelines and regulations. The candidate must remain current on trends and patterns in the health sciences/allied science and medical research fields and regulations governing IND/IDEs.
  • Reviews, adverse drug reaction reports to determine the implications for current and planned research, and initiates necessary actions, including modification of specific protocol and overall drug development plans.
  • Provides leadership and direction for the following functions: Protocol Development and Review; Development, Support, and Oversight of Clinical Trial Procedures; Training and Quality Assurance Functions; and Liaison, Coordination, and Advisory Functions.

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 the pre-appointment process (i.e., background investigation, verification of qualifications and job requirements, completion of onboarding forms, submission of required documents, etc.)
  • Males born after December 31, 1959 must be registered with the Selective Service.
  • Applicants must meet all qualifications requirements within thirty (30) calendar days of the closing date of this announcement, including time in grade.
  • Position requires Education. Please submit transcript(s).
  • A one-year supervisory trial/probationary period may be required upon selection/placement.

Qualifications

In order to qualify for a Supervisory Regulatory Operations Specialist, GS-0601, position you must have successfully completed a bachelor's degree or graduate/higher level degree with major study in an academic field related to the medical field, health sciences or allied sciences appropriate to the work of the position. (This degree must be from an educational program from an accrediting body recognized by the U.S. Department of Education at the time the degree was obtained).

In addition, in order to qualify for a Supervisory Regulatory Operations Specialist, GS-0601-15, you must have at least one year of qualifying specialized experience equivalent to at least the GS-14 level in the Federal Government obtained in either the private or public sector, performing the following types of tasks: providing leadership, oversight, and guidance on regulatory requirements for clinical trials for Investigational New Drug and Investigational Device Exemption applications; providing expertise and guidance on regulations, policies, and procedures governing clinical trials operations and regulatory applications; overseeing the preparation of reports on clinical trials operations and regulatory issues; overseeing and providing guidance on the development of clinical trial protocols; and providing supervision and direction to other staff.

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.

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.

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 with 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 knowing your past accomplishments or experience in your application may be contacted for verification purposes at any time. Verification may, but need not, begin before receiving an offer.??

Preview assessment questionnaire before you apply: https://apply.usastaffing.gov/ViewQuestionnaire/12484227

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 "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.
  • You may qualify for reimbursement of relocation expenses in accordance with agency policy.
  • If selected, you will be required to complete a Confidential Financial Disclosure Report, OGE Form 450 to determine if a conflict or an appearance of a conflict exists between your financial interest and your prospective position with the agency. This information is required annually. For information, visit the NIH Ethics website: https://ethics.od.nih.gov/topics/fd.html.
  • A newly appointed or reappointed employee may receive service credit for prior work experience or active duty uniformed service that otherwise would not be creditable for the purpose of determining his or her annual leave accrual rate. All creditable service must be directly related to the duties of the position being filled and decisions to allow for such credit must be finalized prior to the selectee's entrance on duty. Recipients will be determined on a case-by-case basis based on organizational need, specific case justification, and budget limitations.
  • A one-year probationary period may be required upon selection/placement.
  • PHS Commissioned Officers interested in performing the duties of this position within the Commissioned Corps should apply online to this announcement to receive consideration.
  • Veterans' Preference applies only to Schedule A (disability appointment) and Veterans Recruitment Appointments (if applicable).
  • 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 supervision and direction to other staff.
  • 2) Skill in managing clinical and operational activities for clinical trials for cancer research.
  • 3) Skill in clinical trial protocol development and review.
  • 4) Knowledge of the regulations, policies, and procedures governing clinical trials.


Additional selections may be made for similar positions across the Department of Health and Human Services (HHS) within the local commuting area(s) of the location identified in this announcement. By applying, you agree to have your application shared with interested selecting official(s) at HHS. Clearance of CTAP/ICTAP will be applied for similar positions across HHS.

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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