Deputy Center Director

Alohma LLC

$120K — $150K *
Education, Government & Non-Profit
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • 5-10 years of executive level management experience in scientific or regulatory fields.
  • Strong knowledge of FDA regulatory processes and policies.
  • Proven leadership in directing large organizations and implementing policies.
  • Excellent communication skills for diverse and geographically dispersed teams.
  • Extensive experience in the regulation of biological products.
  • Advanced degree in law, science, or management preferred.

Responsibilities

  • Collaborate with the Center Director to oversee all center operations and initiatives.
  • Act as the Deputy Center Director, representing leadership in their absence.
  • Advise on strategic initiatives and regulatory policy decisions.
  • Establish governance practices for effective policymaking across the center.
  • Monitor policy development and implementation activities with office directors.
  • Prepare and present comprehensive materials on substantive issues and proposals.
  • Lead strategic engagement with Congress and stakeholders on legislative matters.

Benefits

  • Opportunity for career advancement within a key federal agency.
  • Engagement in high-impact public health initiatives.
  • Participatory role in shaping national regulatory policies.
  • Access to professional development resources and training opportunities.
  • Flexible working arrangements may be available.
Full Job Description
Summary

This position is being filled under a stream-lined hiring authority, Title 21 of the United States Code (21 US Code 379d-3a) as amended by the 21st Century Cures Act of 2016, section 3072 and the Consolidated Appropriations Act of 2023, Section 3624. The candidate selected for this position will serve under a career or career-conditional appointment and be paid under the provisions of this authority. This position is being recruited based on the Title 21 Pay Table 4, BandH.

Duties

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  • As the Deputy Center Director, participates fully with the Center Director in planning, managing, organizing, and directing all operations, programs segments, functions, and activities of the Center.
  • Represents the Center Director and serves as the Acting Center Director in his or her absence.
  • Serves to organize and coordinate matters brought to the attention of the Office of the Center Director and acts as an advisor to the Center Director on issues requiring decisions based upon comprehensive reviews of the issues.
  • Acts as a principal policy advisor to the Center Director on issues that require the most careful analysis concerning strategic initiatives and regulatory policy programs for CBER.
  • Establishes and maintains effective Center-wide governance and clearance mechanisms for advancing policymaking within the CBER and in collaboration with other FDA Centers and Offices.
  • Participates with the Office Directors in monitoring policy development and policy implementation activities of interest to the Center Director. Evaluates Center-wide ongoing biological product policies.
  • Develops, prepares, and presents authoritative memoranda, briefings, position papers and other materials concerning substantive questions, issues, findings, conclusions and proposed solutions and suggested courses of action.
  • Collaborates with the Center Director and Agency leaders to develop policy on pre-market product access and approvals, labeling, exclusivity and incentives, and emerging biological technologies and tools, including for cross-Center coordination.
  • Directs special studies and workgroups on major issues, reviewing and evaluating Center programs and consulting with Agency officials to address problems with regional, national, and international impact, and recommending actions to resolve them.
  • Provides authoritative guidance to leadership on short- and long-term activities to maximize CBER's public health impact; reviews and analyzes program reports, proposals, memoranda, and other materials affecting Center operations.
  • Shares responsibility with the Center Director to identify opportunities, develop strategies, and cross-Center projects. Oversees improvements in governance, hiring, and strategic planning while building strong coalitions.
  • Leads the Center's strategic engagement on legislative issues, representing the Center with Congress and stakeholders, guiding positions on legislation, and developing implementation plans following enactment of new laws.


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.
  • The candidate selected for this position will serve under a career or career-conditional appointment within the competitive service.
  • Direct Deposit: You will be required to have all federal salary payments electronically deposited into a bank account with a financial institution of your choice.


Qualifications

In order to qualify for the Deputy Center Director position which falls under the 0601 occupational Series, you must meet the following requirements by 11:59 pm EST on 08/05/2026:

The candidate must meet the following qualifications for this Title 21 position:

  1. Scientific, Technical, and/or Professional Fields
  2. Qualified and Outstanding Candidates


a. Qualified applies to all candidates for Cures appointments. The FDA OTS will use the technical qualifications defined below as a baseline for comparing experience levels and other candidate attributes for relevant positions

b, Outstanding candidates can be defined by existing outstanding work experience, outstanding performance rating, or both.

Technical Requirements: (Please do not submit narrative responses these qualifications must be included in your 2-page resume)

  1. Executive Level experience directing a large organization.
  2. Experience establishing organizational policy, including the implementation of new legislative authorities or other significant mandates.
  3. Demonstrated ability to communicate effectively both internally and externally to a large number of staff located in different geographic areas.
  4. Demonstrated ability and experience coordinating complex work and priorities and building coalitions with partners in other organization.
  5. Extensive experience and knowledge of the FDA's regulatory and review process; strong leadership and significant executive management experience.
  6. Demonstrated knowledge and experience in the regulation and development of biological products, including the evaluation of safety, effectiveness, and product quality.


Desired Qualifications:

  1. Knowledge of Federal laws and regulations and DHHS and FDA policies and procedures.
  2. Talent for leading cultural and organizational change management efforts.
  3. Knowledge and awareness of the Director's interests and objectives in all matters involving the application of regulatory and policy judgement.
  4. Experience interacting with the media and with entities that perform oversight activities, such as Congress or the General Accountability Office or a Board of Directors.
  5. An advanced degree in law, science or management from an accredited college or university.


NOTE: Applicants must submit all relevant transcripts that demonstrate you possess the required education to meet the Basic Qualifications.

Supervisory Responsibilities The incumbent is delegated full authority to achieve group goals and objectives through the effective management of available resources. Performance and accomplishments are assessed primarily through work performance indicators, staff discussion, planning sessions, review of individual project outputs, and annual program review.

Leads in a proactive, customer-responsive manner consistent with Agency vision and values, effectively communicating program issues to external audiences. Ensures financial and managerial accountability by acting with prudence when executing fiduciary responsibilities. Demonstrates high integrity and adheres to the highest ethical standards of public service. Uses effective business practices including balanced measures of results, values, and invests in each employee; emphasizes empowerment and two-way communication. Takes a leadership role in advocating for and advancing the priorities of the Agency. Serves as a role model for leadership by encouraging teamwork and a collaborative approach. Timely notifies Agency officials of all significant actions and developments, including but not limited to those related to regulatory matters, legislative matters, budget matters, reports, initiatives, and events and ensures subordinate managers do the same.

Provides reasonable accommodations needed to best utilize qualified people with disabilities.

Organizational Management:

Program Management:

Resource Management:

Personnel Performance Management:

Human Capital Management:

This position is designated as an SES Equivalent position and is covered under the FDA Title 21 Executive Performance Management System and identified as a public filing position for ethics purposes.

Drug Impact Statement for Top Secret Security Clearance: The position requires a Top-Secret/Sensitive Compartmented Information (TS/SCI) security clearance, and the incumbent has access to documents and facilities related to national security.

Ethics Preclearance Requirements

This position requires financial disclosure reporting and will be subject to FDA's prohibited financial interest regulation. If you are hired, you may be required to divest of certain financial interests. You are advised to seek additional information on this requirement from the hiring official before accepting any job offers. For more information, please visit the FDA Ethics web page: https://www.fda.gov/about-fda/jobs-and-training-fda/ethics.

All requirements must be met by the closing date of this announcement (08/05/2026); only education and experience gained by this date will be considered. You must continue to meet all requirements throughout the entire hiring process.

Education

Pay careful attention to the Qualifications and Education sections to identify vacancies where a transcript is required. Even if you hold a similar position or are a current employee, you are not exempt from transcript requirements.

Education Requirement: Bachelor's or graduate/higher level degree: major study in an academic field related to the medical field, health sciences or allied sciences appropriate to the work of the position.

TRANSCRIPTS: Positions which are scientific or technical in nature often have very specific educational requirements. You must submit an official transcript, unofficial transcript, including courses, grades earned, completion dates, and quarter and semester hours earned.

Education must be accredited by an accrediting institution recognized by the U.S. Department of Education in order for it to be credited towards qualifications. Therefore, provide only the attendance and/or degrees from schools accredited by accrediting institutions recognized by the U.S. Department of Education.

If you are using education completed in foreign colleges or universities, see the Foreign Education section below for additional requirements.

Electronic Transcript Caution: If you have obtained your transcripts electronically, the file might contain security measures that could prevent our application system from reading the file. Therefore, you should consider asking the institution to provide the file in a non-secured electronic format. Alternatively, you could scan or take a photo of the printed copy of the transcript. If your uploaded transcript cannot be read by our system, you may receive consideration and credit for the information we can access.

Foreign Education: If you are using education completed in foreign colleges or universities to meet the qualification requirements, you must show that the education credentials have been evaluated by a private organization that specializes in interpretation of foreign education programs and such education has been deemed equivalent to that gained in an accredited U.S. education program; or full credit has been given for the courses at a U.S. accredited college or university. For further information, visit the U.S. Department of Education website for Foreign Education Evaluation.

To be acceptable, the foreign credential evaluation must include/describe at a minimum, the following information: (1) The type of education received by the applicant; (2) The level of education in relation to the U.S. education system, and state that its comparability recommendations follow the general guidelines of the International Eval

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