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Director Policy Analyst Jobs in Raleigh, NC (NOW HIRING)

Supports the firm's Practice Group Directors in their oversight of the firm's critical business ... Comply with all firm policies and practices. * Engage in both physical and sedentary activity, such ...

Director, Human Resources

Chapel Hill, NC ยท On-site

$125K - $145K/yr

... provide analytical workforce snapshots for leadership. * Compliance & Policy: Ensure strict ... Director role at a company with >250 employees (500+ preferred). * Strong data and analytical ...

Overview POSITION TITLE (Oracle title) SENIOR DIRECTOR WORKING TITLE Senior Director-Talent ... policy. Serves as an essential partner in district efforts to analyze and improve employee ...

Our direct client has a new opening for a Lead Security Analyst 141809 This job is 14 months to ... policy implementation Incident response & threat mitigation Preferred Skills Experience with ...

Continuously enhances the data and analytics capabilities of Biostatistics and Statistical ... policies, practices, and procedures. * Identify training and development needs of direct reports ...

... direct deposit maintenance, terminations, leave of absences, wage garnishments, stock and equity ... Follow payroll procedures while interpreting and evaluating policies and procedures and suggesting ...

... of policies and procedures. The Closing team works in tandem with the Risk Management team to ... Collaborating with internal staff to prepare investment reports, to review key analytics and ...

Showing results 41-60

Director Policy Analyst information

See Raleigh, NC salary details

$40.3K

$94.2K

$133.2K

How much do director policy analyst jobs pay per year?

As of Aug 8, 2026, the average yearly pay for director policy analyst in Raleigh, NC is $94,215.00, according to ZipRecruiter salary data. Most workers in this role earn between $65,100.00 and $113,200.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a director policy analyst?

To thrive as a Director Policy Analyst, you need advanced analytical skills, expertise in policy development, and typically a master's degree in public policy, political science, or a related field. Familiarity with data analysis tools, legislative tracking systems, and policy research databases is important for effective performance. Strategic thinking, persuasive communication, and stakeholder management are critical soft skills that distinguish successful leaders in this role. These competencies ensure informed policy recommendations, effective advocacy, and the ability to navigate complex regulatory environments.

What is the difference between Director Policy Analyst vs Policy Analyst?

AspectDirector Policy AnalystPolicy Analyst
ResponsibilitiesOversees policy development, manages teams, and sets strategic goalsResearches, analyzes, and develops policy recommendations
CredentialsBachelor's or master's degree, often with experience in leadership rolesBachelor's or master's degree in public policy, political science, or related fields
Work EnvironmentSenior-level position in government agencies, think tanks, or NGOsEntry to mid-level roles in similar organizations
FocusStrategic planning and policy oversightData analysis and policy research

The main difference is that a Director Policy Analyst leads and manages policy teams and strategies, while a Policy Analyst focuses on research and analysis to inform policy decisions. The director role involves higher-level responsibilities and leadership, whereas the analyst role is more focused on detailed research and recommendations.

What does a director policy analyst do?

A Director Policy Analyst leads teams in researching, developing, and evaluating public policies for organizations, government agencies, or advocacy groups. They analyze complex policy issues, interpret legislation, and make recommendations to senior leadership. The director often shapes strategic objectives, oversees policy research projects, and communicates findings to stakeholders or the public. Additionally, they may represent their organization in meetings or public forums and help to guide the policy direction based on evidence and best practices.

How does a director policy analyst typically collaborate with stakeholders to shape policy recommendations?

A Director Policy Analyst frequently works with a diverse range of stakeholders, including government officials, community leaders, industry experts, and internal teams, to gather insights and feedback on policy issues. Collaboration often involves organizing meetings, leading workshops, and facilitating open communication to ensure all perspectives are considered in the analysis. This cross-functional teamwork is crucial for developing well-informed, practical policy recommendations that address the needs and concerns of various groups. Building and maintaining strong professional relationships is a key part of the role, as it enhances the quality and impact of policy initiatives.
What are the most commonly searched types of Policy Analyst jobs in Raleigh, NC? The most popular types of Policy Analyst jobs in Raleigh, NC are:
What are popular job titles related to Director Policy Analyst jobs in Raleigh, NC? For Director Policy Analyst jobs in Raleigh, NC, the most frequently searched job titles are:
What job categories do people searching Director Policy Analyst jobs in Raleigh, NC look for? The top searched job categories for Director Policy Analyst jobs in Raleigh, NC are:
Infographic showing various Director Policy Analyst job openings in Raleigh, NC as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 17% Part Time, and 4% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $94,215 per year, or $45.3 per hour.

Associate Director or Director, CMC Regulatory Affairs

Atsena

Durham, NC โ€ข On-site

$180 - $260/hr

Other

Posted 22 days ago


Job description

Position Summary

The Associate Director / Director, CMC Regulatory Affairs will lead global CMC regulatory strategy and execution for the companyโ€™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
  • 7โ€“10 years of experience in regulatory affairs and CMC.
  • Experience contributing to CMC sections of IND/CTA submissions.
Director Experience
  • 10โ€“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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