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Pharmaceutical State Licensing Project Manager Jobs in Raleigh, NC

... pharmaceutical client's team, you will manage projects from initial intake through final delivery. You will coordinate cross-functional stakeholders, multilingual content, copyright and licensing ...

New

Pharmaceutical, biotech, or life sciences industries. * OR other regulated manufacturing ... Licenses & Certifications: * PMP certification or progress toward certification is a plus. * CAPM ...

Pharmaceutical, biotech, or life sciences industries. * OR other regulated manufacturing ... Licenses & Certifications: * PMP certification or progress toward certification is a plus. * CAPM ...

... for the world's pharmaceutical, biotech and medical device industries. We do this across six ... Works in the role of a project manager on assigned project(s), which may range from single service ...

... for the world's pharmaceutical, biotech and medical device industries. We do this across six ... Works in the role of a project manager on assigned project(s), which may range from single service ...

Pharmaceutical, biotech, or life sciences industries. * OR other regulated manufacturing ... Licenses & Certifications: * PMP certification or progress toward certification is a plus. * CAPM ...

Construction Project Manager

Durham, NC ยท On-site

$51 - $53/hr

Project/Program Manager - Non IT III (Construction Project Manager) Location: Durham, NC (Onsite ... Experience with commercial, laboratory, healthcare, pharmaceutical, or life sciences facilities ...

Showing results 21-40

Pharmaceutical State Licensing Project Manager information

See Raleigh, NC salary details

$32.6K

$70.9K

$113.2K

How much do pharmaceutical state licensing project manager jobs pay per year?

As of Aug 9, 2026, the average yearly pay for pharmaceutical state licensing project manager in Raleigh, NC is $70,860.00, according to ZipRecruiter salary data. Most workers in this role earn between $53,000.00 and $84,100.00 per year, depending on experience, location, and employer.

What does a pharmaceutical state licensing project manager do?

A Pharmaceutical State Licensing Project Manager oversees and coordinates the process of obtaining and maintaining state licenses required for pharmaceutical operations. This role involves managing applications, ensuring compliance with state regulations, tracking renewals, and communicating with regulatory agencies. The project manager works closely with legal, regulatory, and operational teams to ensure all licensing requirements are met efficiently. Their work helps prevent interruptions in business operations and supports the company's expansion into new markets.

What is the difference between Pharmaceutical State Licensing Project Manager vs Pharmaceutical Regulatory Specialist?

AspectPharmaceutical State Licensing Project ManagerPharmaceutical Regulatory Specialist
CredentialsTypically requires a bachelor's degree in life sciences or related field; certifications like RAC are commonSimilar credentials, often with RAC certification and relevant degrees
Work EnvironmentProject-based roles coordinating licensing across states, often within pharmaceutical companies or consulting firmsRegulatory compliance focus, working within pharmaceutical companies or regulatory agencies
Industry UsageUsed in pharmaceutical companies managing licensing projectsCommon in regulatory affairs departments
Search & Comparison IntentOften compared for licensing and project management rolesCompared for regulatory compliance and documentation expertise

The Pharmaceutical State Licensing Project Manager primarily oversees licensing projects across states, coordinating efforts to ensure compliance. The Pharmaceutical Regulatory Specialist focuses on regulatory documentation and compliance within the industry. While both roles require similar credentials and work environments, their core responsibilities differ: one manages licensing projects, the other ensures regulatory adherence.

What are the key skills and qualifications needed to thrive as a pharmaceutical state licensing project manager, and why are they important?

To thrive as a Pharmaceutical State Licensing Project Manager, you need in-depth knowledge of regulatory compliance, project management expertise, and experience in pharmaceutical licensing processes, often supported by a relevant degree and PMP certification. Familiarity with compliance management software, project tracking systems, and state-specific licensing databases is typically required. Exceptional attention to detail, organizational skills, and strong communication abilities help in coordinating between regulatory bodies and internal stakeholders. These skills ensure timely and accurate licensure, reducing compliance risks and enabling the business to operate smoothly across multiple states.

What are some common challenges faced by pharmaceutical state licensing project managers when coordinating multi-state licensing projects?

Pharmaceutical State Licensing Project Managers often encounter challenges such as navigating varying state regulations, aligning timelines for multiple applications, and ensuring documentation accuracy for each jurisdiction. Coordinating with cross-functional teams, such as legal, compliance, and operations, is essential to keep projects on track. Staying organized and proactive in communication is key, as delays in one state can impact overall project goals and company market access. Effective project managers leverage detailed tracking systems and maintain regular stakeholder updates to mitigate these challenges.
What are popular job titles related to Pharmaceutical State Licensing Project Manager jobs in Raleigh, NC? For Pharmaceutical State Licensing Project Manager jobs in Raleigh, NC, the most frequently searched job titles are:
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What cities near Raleigh, NC are hiring for Pharmaceutical State Licensing Project Manager jobs? Cities near Raleigh, NC with the most Pharmaceutical State Licensing Project Manager job openings:

Senior Project Manager, COA

110 ICR Ireland - IRE

Raleigh, NC โ€ข Remote

Full-time

Posted 3 days ago

New


Job description

Senior Project Manager, COA-ICON- US Remote (East Coast)

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.


As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.


Title: Senior Project Manager, COA

Location: Remote - USA (East Coast)

What you will do:  As a Senior Project Manager within Patient Centered Solutions and Language Services at ICON, you will lead the delivery of clinical outcome assessment localization and electronic Clinical Outcome Assessment programs across multiple clinical studies. Serving as an embedded extension of a key pharmaceutical client’s team, you will manage projects from initial intake through final delivery. You will coordinate cross-functional stakeholders, multilingual content, copyright and licensing activities, eCOA migrations, quality reviews, and project documentation. You will also help improve operational processes, reduce delivery timelines, and support the evaluation of new automation technologies.

Key responsibilities include:

  • Serve as the primary operational contact for incoming localization and eCOA requests, coordinating project kickoffs with study teams and other stakeholders.
  • Develop and manage project plans, requirements, timelines, deliverables, risks, and resource needs across multiple concurrent global and local studies.
  • Lead cross-functional collaboration among client stakeholders, study teams, localization specialists, technology teams, copyright holders, vendors, and other internal and external partners.
  • Assess the availability and readiness of questionnaires, translations, licenses, and supporting assets before translation and eCOA migration activities begin.
  • Coordinate copyright licensing, source-content review, translation preparation, multilingual deliverables, content modifications, and version-management activities.
  • Oversee automation-enabled eCOA questionnaire migrations and evaluate outputs for linguistic, formatting, technical, and content-readiness issues.
  • Identify and document migration defects, support root-cause analysis, recommend corrective actions, and provide structured feedback to technology teams.
  • Monitor project quality, timelines, review cycles, productivity, and stakeholder satisfaction through dashboards and status reporting.
  • Maintain complete, accurate, version-controlled, and audit-ready project documentation within approved SharePoint and document-management systems.
  • Identify opportunities to reduce bottlenecks, improve content reuse, shorten migration timelines, reduce manual effort, and standardize processes.
  • Support the validation and implementation of automation, artificial intelligence, and other emerging technologies used in localization and eCOA delivery.
  • Provide project leadership and guidance to cross-functional contributors while promoting quality, collaboration, and continuous improvement.

Your Profile:

  • Bachelor’s degree in Life Sciences, Languages, Translation, Clinical Research, Healthcare Administration, Project Management, or a related discipline.
  • At least five years of relevant experience in clinical localization, clinical operations, clinical technology, or project management within a pharmaceutical, biotechnology, CRO, or related environment.
  • Demonstrated experience managing multiple concurrent projects, timelines, risks, deliverables, and cross-functional stakeholders in a fast-paced, matrix environment.
  • Strong understanding of multilingual content development, translation, and localization workflows.
  • Excellent communication, stakeholder-management, organizational, analytical, and problem-solving skills, with strong attention to detail.
  • Experience using SharePoint, document-management systems, collaboration platforms, and project-tracking tools.
  • Ability to work independently, manage competing priorities, and maintain complete, accurate, and audit-ready project documentation.
  • Direct experience with Clinical Outcome Assessments, electronic Clinical Outcome Assessments, and questionnaire migration projects is highly preferred.
  • Experience with copyright licensing, content acquisition, translation preparation, and version-management processes is highly preferred.
  • Familiarity with eCOA platforms, localization technologies, translation-management systems, or comparable clinical technologies is preferred.
  • Experience reviewing migration outputs, documenting defects, performing root-cause analysis, or supporting quality-validation activities is preferred.
  • Experience supporting automation, artificial intelligence, or clinical-technology pilot programs is preferred.
  • PMP or an equivalent project-management certification is preferred.

Employment with ICON is contingent upon having the legal right to work in the country where the role is based.


Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.


Benefits may include:

  • Competitive base salary and performance related incentives
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.


Visit our careers site to read more about the benefits ICON offers.


Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.


If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.

Are you a current ICON Employee? Please click here to apply