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Agency Director Jobs in Raleigh, NC (NOW HIRING)

MERGE

Account Director - Pharma / Life Science

Raleigh, NC · Hybrid

$88K - $129K/yr

You will work closely with the account team to drive tactical projects through the agency and meet ... Our Account Director- Life Science Practice Area will be upbeat, optimistic, solution-oriented, and ...

Blue Castle Agency

Regional Director

Durham, NC · On-site

$165K - $185K/yr

Regional Director Richmond, VA & Durham, NC $165,000 - $185,000 / year (DOE) OVERVIEW A well-established, owner-operated multifamily organization is seeking a Regional Director to lead asset ...

StepUp Ministry

Be Seen First

Program Director (Life Skills Academy Program Director)

Raleigh, NC · On-site

$60K - $70K/yr

... agencies, or resolving complaints. • Establish a follow-through routine to ensure program ... and directors to support the growth of different departments. • Cultivate and grow the Life ...

UHS

DIR - HIM/MEDICAL RECORDS

Raleigh, NC · On-site

Direct the Health Information Management Service Department within all standards established by regulatory and licensing agencies. * Consult with management, administration, and medical staff to ...

UHS

DIR - HIM/MEDICAL RECORDS

Raleigh, NC · On-site

Direct the Health Information Management Service Department within all standards established by regulatory and licensing agencies. * Consult with management, administration, and medical staff to ...

Therapy Smarts, Inc

ABA Program Director

Chapel Hill, NC · On-site

$100K - $120K/yr

The ABA Program Director will present with a passion for working with children and families in a ... Lead and manage all aspects of the agency's operations, including program development, staff ...

Therapy Smarts Inc

ABA Program Director

Chapel Hill, NC

$100K - $120K/yr

The ABA Program Director will present with a passion for working with children and families in a ... Lead and manage all aspects of the agency's operations, including program development, staff ...

Targetbase

Senior Director, Strategy

Raleigh, NC · On-site

$150 - $210/hr

## Senior Director, StrategyApplyremote type: Hybridlocations: Raleigh, North Carolina, United States ... Agency:**Targetbase **Job Function:**Strategy and Planning **Job Subfunction:**Account Planning and ...

Sage-Truck-Driving-School

School Director

Durham, NC · On-site

$75 - $110/hr

The Director is responsible for the overall day-to-day and long-term administration and management ... agencies; · Responsibility for attendance, testing, grading, and student files; · Invoice for ...

TriMark Digital

Director of Design Services

Raleigh, NC · On-site

$120 - $180/hr

As a performance marketing agency, we believe great design does more than look good--it drives ... direct mail, sales materials, and other marketing and communications initiatives. * Ensure all ...

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All JobsAgency JobsAgency Director JobsAgency Director Jobs in Raleigh, NC

Agency Director information

See Raleigh, NC salary details

$40.3K

$78.6K

$115.7K

How much do agency director jobs pay per year?

As of Sep 4, 2026, the average yearly pay for agency director in Raleigh, NC is $78,645.00, according to ZipRecruiter salary data. Most workers in this role earn between $50,500.00 and $108,400.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as an agency director?

To thrive as an Agency Director, you need strong leadership, strategic planning, and financial management skills, typically supported by a degree in business, management, or a related field. Familiarity with project management software, CRM systems, and relevant industry certifications such as PMP or agency-specific credentials is often expected. Exceptional communication, decision-making, and team-building abilities help set outstanding Agency Directors apart. These skills are crucial for ensuring the agency meets its goals, maintains client satisfaction, and operates efficiently in a competitive environment.

What are some common challenges agency directors face when leading a team, and how can they effectively address them?

Agency Directors often encounter challenges such as managing diverse client expectations, aligning team members with agency goals, and adapting to rapid changes in the industry. Effective communication, fostering a collaborative work environment, and providing ongoing professional development help address these hurdles. Regular check-ins and transparent goal-setting also empower teams to stay motivated and aligned with both client and organizational objectives.

What does an agency director do?

An agency director oversees the operations, strategic planning, and management of an agency or organization. They coordinate staff, develop policies, ensure compliance, and work to meet organizational goals, often requiring leadership skills and experience in administration or management. The role may also involve budgeting, client relations, and reporting to stakeholders.

What are the most commonly searched types of Agency jobs in Raleigh, NC?

The most popular types of Agency jobs in Raleigh, NC are:

What cities near Raleigh, NC are hiring for Agency Director jobs?

Cities near Raleigh, NC with the most Agency Director job openings:

Agency Director jobs near you
Infographic showing various Agency Director job openings in Raleigh, NC as of August 2026, with employment types broken down into 2% As Needed, 70% Full Time, 11% Part Time, and 17% Contract. Highlights an 89% Physical, 3% Hybrid, and 8% Remote job distribution, with an average salary of $71,529 per year, or $34.4 per hour.

Associate Director or Director, CMC Regulatory Affairs

Atsena

Durham, NC • On-site

$180 - $260/hr

Other

Re-posted 19 days ago

Job description

Position Summary

The Associate Director / Director, CMC Regulatory Affairs will lead global CMC regulatory strategy and execution for the company’s gene therapy programs from early research through clinical development and commercialization. This role is responsible for developing CMC regulatory strategies across product development stages, supporting regulatory submissions, and serving as the regulatory liaison to internal CMC teams and external contract manufacturing organizations.

The individual will work cross-functionally with process development, analytical development, manufacturing, quality, and program leadership to ensure that CMC development plans meet regulatory expectations for gene therapy products. The role will also support interactions with global regulatory authorities such as the U.S. Food and Drug Administration and the European Medicines Agency.

Key Responsibilities CMC Regulatory Strategy
  • Develop and implement global CMC regulatory strategies for gene therapy programs from early development through clinical stages and commercialization.
  • Provide regulatory guidance on viral vector manufacturing, process development, analytical characterization, and product comparability.
  • Assess regulatory risks related to manufacturing changes and propose mitigation strategies.
Regulatory Submissions
  • Lead preparation and review of CMC sections of global regulatory submissions, including: INDs and IND amendments, CTAs and IMPDs, BLA/MAA submissions and supplements, annual reports and regulatory updates
  • Ensure submissions meet regulatory expectations for gene therapy products.
Health Authority Interactions
  • Prepare CMC regulatory briefing documents and support agency meetings.
  • Serve as the subject matter expert for CMC topics during interactions with agencies including the FDA and EMA.
  • Coordinate and author responses to regulatory agency questions related to CMC.
Cross-Functional Collaboration
  • Partner closely with internal teams including: Process Development, Analytical Development, Manufacturing, Quality
  • Serve as the CMC regulatory representative on cross-functional program teams.
  • Provide regulatory guidance for manufacturing changes, comparability strategies, and lifecycle management.
Regulatory Intelligence & Compliance
  • Monitor evolving regulatory guidance related to gene therapy and advanced biologics.
  • Interpret regulatory requirements and communicate implications to internal teams.
  • Support development of internal regulatory policies and processes.
Qualifications Education
  • PhD or MS in biochemistry, molecular biology, chemical engineering, pharmaceutical sciences, or related field.
Preferred Qualifications
  • Direct experience with AAV, lentiviral, or other gene therapy platforms.
  • Experience supporting late-stage development or BLA/MAA submissions.
  • Familiarity with global regulatory frameworks for advanced therapy medicinal products (ATMPs).
  • Prior experience participating in regulatory meetings.
Associate Director Experience
  • 7–10 years of experience in regulatory affairs and CMC.
  • Experience contributing to CMC sections of IND/CTA submissions.
Director Experience
  • 10–15+ years of experience in regulatory affairs with leadership responsibility for CMC regulatory strategy.
  • Demonstrated experience leading CMC regulatory submissions and health authority interactions.
Knowledge & Skills
  • Strong knowledge of global CMC regulatory requirements for biologics and gene therapies.
  • Understanding of viral vector manufacturing processes.
  • Experience with analytical characterization, comparability, and manufacturing changes.
  • Excellent regulatory writing and communication skills.
  • Ability to work effectively in a fast-paced startup environment.
Key Competencies
  • Strategic thinking and problem solving
  • Strong scientific and regulatory expertise
  • Cross-functional leadership
  • Excellent communication and collaboration skills
  • Ability to manage multiple programs and timelines
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