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Associate Director Pharmaceutical Jobs in Raleigh, NC

Senior Integrated Clinic Pharmacist

Raleigh, NC · On-site

$115K - $137K/yr

You will report to a Associate Director, Integrated Clinical Pharmacist. You will: * Use evidence-based medicine and clinical judgment to evaluate the suitability of pharmacotherapy for high-risk ...

Senior Integrated Clinic Pharmacist

Raleigh, NC · On-site

$115K - $137K/yr

You will report to a Associate Director, Integrated Clinical Pharmacist. You will: * Use evidence-based medicine and clinical judgment to evaluate the suitability of pharmacotherapy for high-risk ...

Supervises Associate Directors to ensure the client projects and strategic initiatives are ... Pharmaceutical / CRO experience * Ability to manage through metrics * Ability to project manage

Showing results 21-40

Associate Director Pharmaceutical information

See Raleigh, NC salary details

$73.4K

$160.2K

$255.2K

How much do associate director pharmaceutical jobs pay per year?

As of Aug 10, 2026, the average yearly pay for associate director pharmaceutical in Raleigh, NC is $160,196.00, according to ZipRecruiter salary data. Most workers in this role earn between $118,100.00 and $194,400.00 per year, depending on experience, location, and employer.

What is an associate director pharmaceutical?

An Associate Director in the pharmaceutical industry is a leadership role responsible for overseeing various functions such as drug development, regulatory affairs, clinical operations, or commercialization. They provide strategic direction, ensure compliance with industry regulations, and collaborate with cross-functional teams to drive projects forward. This role requires extensive experience, leadership skills, and a deep understanding of pharmaceutical processes. Typically, an Associate Director works closely with senior executives to align business objectives with regulatory and scientific requirements.

What types of teams or departments does an associate director pharmaceutical typically collaborate with?

Associate Directors in the pharmaceutical industry often work closely with multidisciplinary teams, including clinical development, regulatory affairs, quality assurance, medical affairs, and commercial operations. They facilitate communication between departments to synchronize timelines, ensure regulatory compliance, and drive product development forward. Collaboration may also extend to external partners such as contract research organizations (CROs) or regulatory agencies. This cross-functional interaction is essential to efficiently manage resources, resolve challenges, and support organizational goals.

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

To thrive as an Associate Director Pharmaceutical, you need an advanced degree in pharmacy, life sciences, or a related field, plus significant experience in pharmaceutical development or regulatory affairs. Familiarity with clinical trial management systems, regulatory submission software, and certifications such as PMP or RAC are highly valued. Strong leadership, strategic thinking, and interpersonal communication set standout candidates apart. These skills and qualifications are crucial for overseeing cross-functional teams, ensuring regulatory compliance, and successfully managing complex projects within the pharmaceutical industry.

What job categories do people searching Associate Director Pharmaceutical jobs in Raleigh, NC look for? The top searched job categories for Associate Director Pharmaceutical jobs in Raleigh, NC are:
What cities near Raleigh, NC are hiring for Associate Director Pharmaceutical jobs? Cities near Raleigh, NC with the most Associate Director Pharmaceutical job openings:
Infographic showing various Associate Director Pharmaceutical job openings in Raleigh, NC as of August 2026, with employment types broken down into 1% As Needed, 68% Full Time, 28% Part Time, 1% Temporary, and 2% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $160,196 per year, or $77 per hour.

Associate Director/Director, Program Design Biologics

Fujifilm

Morrisville, NC • On-site

Full-time

Re-posted 25 days ago


Fujifilm rating

8.4

Company rating: 8.4 out of 10

Based on 67 frontline employees who took The Breakroom Quiz

50th of 538 rated manufacturers


Job description

We’re growing and seeking an accomplished biologics professional to join our Program Design team. In this role, you will partner closely with our global commercial sales organization and site technical/operations teams to shape winning, customertailored programs—from technology transfer through cGMP manufacturing and process validation.

You will lead technical discussions with prospective and current clients, translate complex needs into clear program designs and proposals, and help drive new business across FUJIFILM Biotechnologies sites.

Associate Director or Director will be aligned to your experience; the Director level may include people leadership and broader crosssite improvement initiatives.


The work we do at FUJIFILM Biotechnologies has never been more important—and we are looking for talented candidates to join us. We are growing our locations, our capabilities, and our teams, and looking for passionate, mission-driven people like you who want to make a real difference in people’s lives.
Join FUJIFILM Biotechnologies and help make the next vaccine, cure, or gene therapy in partnership with some of the most innovative biopharma companies across the globe. We are proud to cultivate a culture that will fuel your passion, energy, and drive - what we call Genki. 
 
Fujifilm is globally headquartered in Tokyo with over 70,000 employees across four key business segments of healthcare, electronics, business innovation, and imaging. We are guided and united by our Group Purpose of “giving our world more smiles.” Visit: https://www.fujifilm.com/us/en/about/region/careers


What You’ll Do

  • Lead the technical aspects of customer meetings and teleconferences, projecting FUJIFILM’s experience and expertise.
  • Review RFPs and design customer programs spanning process development, technology transfer, cGMP manufacturing, and process validation.
  • Assess customer programs for fit with FUJIFILM Biotechnologies’ capabilities and site requirements.
  • Partner with site operational/technical teams to evaluate program feasibility and requirements.
  • Prepare high-quality proposals in response to RFPs, tailored to customer goals and constraints.
  • Define program scope, siting/location, timelines, and resource needs in alignment with internal and client stakeholders.
  • Support the overall sales process as needed, including SoW development, internal commercial processes, and customer requests.
  • Engage proactively with internal stakeholders and manufacturing teams to promote open communication and enhance our service offerings.
  • Stay current with industry advancements; attend webinars and conferences in support of FUJIFILM commercial teams.
  • At the Director level, lead and direct Program Design team improvement efforts, including harmonization of work practices across sites.
  • At the Director level, manager 1-3 direct reports supporting the FUJIFILM Biotechnologies business.
  • Other duties as assigned.

Required Qualifications (Education and Experience)

  • Education: Scientific degree (Bachelor’s degree) in relevant biological science field.
  • Experience:
    • 8+ years of technical experience in the pharmaceutical/biotechnology industry.
    • Broad understanding of CDMO business models and Biologics manufacturing (Microbial and/or Mammalian).
    • Working knowledge of the regulatory environment, process development, and analytical technologies for biopharmaceutical manufacturing.
    • Demonstrated understanding of, and experience with, cGMP manufacturing and associated requirements.
    • Excellent written and verbal communication skills with the ability to interact with external customers in a professional and personable manner and to present a competent image of FUJIFILM at all times.
    • Proven ability to analyze complex technical problems and present clear, actionable solutions.
    • Ability to influence and collaborate effectively with customers and colleagues at all levels.
    • Any combination of education and experience, which would provide an equivalent background to deliver against role expectations.

 

Preferred Qualifications

  • Education: Advanced scientific degree (e.g. MSc or PhD) in a relevant biological science field.
  • Experience:
    • 6+ years of technical experience in a CDMO or closely related biopharmaceutical environment; experience working directly with customers in a client-facing capacity.
    • Prior experience within FUJIFILM Biotechnologies or another biologics CDMO.
    • Direct experience designing end-to-end programs from technology transfer through validation within a commercial environment.
    • Leadership experience, especially cross-site harmonization and/or managing a small team (for Director consideration).

Who You Are:

  • A customer-centric problem solver who thrives at the intersection of science, operations, and business development.
  • A clear communicator who can translate complex scientific concepts into compelling, solution-oriented proposals.
  • A collaborative partner who builds trust with technical, quality, and commercial teams to deliver on shared goals.

Why Join FUJIFILM Biotechnologies

  • Impact: Shape high-value biologics programs and help customers bring important therapies to patients.
  • Growth: Role scope and title (Associate Director or Director) tailored to your background, with opportunities to lead cross-site initiatives and people.
  • Collaboration: Work with a global, multidisciplinary team across leading biologics sites.

Research shows that some candidates hesitate to apply unless they check every box. If you’re excited about this role and have relevant experience in biologics/CDMO environments—even if your past experience doesn’t align perfectly with every requirement—we encourage you to apply. We’re committed to building a diverse, inclusive, and authentic workplace and welcome applicants from all backgrounds, including internal candidates exploring career growth.

 

To all agencies: Please, no phone calls or emails to any employee of FUJIFILM about this requisition. All resumes submitted by search firms/employment agencies to any employee at FUJIFILM via-email, the internet or in any form and/or method will be deemed the sole property of FUJIFILM, unless such search firms/employment agencies were engaged by FUJIFILM for this requisition and a valid agreement with FUJIFILM is in place. In the event a candidate who was submitted outside of the FUJIFILM agency engagement process is hired, no fee or payment of any kind will be paid.


Fujifilm is committed to providing equal opportunities in hiring, promotion and advancement, compensation, benefits, and training regardless of nationality, age, gender, sexual orientation or gender identity, race, ethnicity, religion, political creed, ideology, national, or social origin, disability, veteran status, etc.


If you require reasonable accommodation in completing this application, interviewing, completing any pre-employment testing, or otherwise participating in the employee selection process, please direct your inquiries to our HR Department (fdbglobaltalent@fujifilm.com).


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About Fujifilm

Sourced by ZipRecruiter

With each Industry we enter, We’ve learned to Leverage and Adapt our knowledge, Expertise and rRsources to make the World a better place. When it comes to Innovating for a Healthier World and a more sustainable society, we’ll NEVER STOP. Fujifilm will contribute to the social challenges by creating new value in a wide range of business domains through innovation in Products, Services, and Technological Development. We launched our Healthcare Business with X-ray film in 1936. And now, We are developing our business in areas of prevention, diagnosis, and treatment as a Comprehensive Healthcare Company. We will never stop Innovating for a Healthier World.

Industry

Chemical manufacturing

Company size

10,000+ Employees

Headquarters location

Minato-ku, Tokyo, JP

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