ZipRecruiter

Log In

1

Associate Director Pharmaceutical Jobs in Raleigh, NC

IQVIA

Associate Director, Medical Reviewer

Durham, NC · Remote

$115K - $322K/yr

Associate Director, Medical Review (MLR) Location : Home-based in USA Job Overview: IQVIA Pharma ... the pharmaceutical industry. As a Final Medical Content Approver, you will act as the primary ...

next page

Showing results 1-20

All JobsAssociate Pharmaceutical JobsAssociate Director Pharmaceutical JobsAssociate Director Pharmaceutical Jobs in Raleigh, NC

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 Sep 12, 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 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 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.

Is an Associate Director Pharmaceutical a high position?

An Associate Director in the pharmaceutical industry is considered a senior management role, often overseeing teams and projects within a department. It typically requires extensive experience, leadership skills, and industry knowledge, making it a high-level position within the organizational hierarchy.

What are popular job titles related to Associate Director Pharmaceutical jobs in Raleigh, NC?

For Associate Director Pharmaceutical jobs in Raleigh, NC, the most frequently searched job titles are:

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:

Associate Director Pharmaceutical jobs near you
Infographic showing various Associate Director Pharmaceutical job openings in Raleigh, NC as of September 2026, with employment types broken down into 89% Full Time, 7% Part Time, and 4% Contract. Highlights an 86% In-person, 7% Hybrid, and 7% Remote job distribution, with an average salary of $160,196 per year, or $77 per hour.

Associate Director, Analytical Sciences

Durham, NC • On-site

implaion
See more jobs at implaionexternal

Full-time

Posted 23 days ago

Key responsibilities

  • Establish and evolve analytical strategies to support the company's development portfolio.

  • Provide scientific leadership for analytical lifecycle management, method validation, and control strategy development.

  • Partner with internal teams and external partners to ensure integrated analytical approaches and support regulatory activities.

Job description

SUMMARY

  • Clinical-stage biotech advancing antibody into Phase 2b
  • Senior scientific leader for analytical strategy — control strategy, comparability, validation, characterization through BLA
  • Direct ownership, no layers; drive the work with CDMOs and external labs

About the Position

The Associate Director, Analytical Sciences will provide scientific leadership and strategic direction for analytical sciences across the biologics development portfolio. Reporting to the Senior Director, Tech Ops, this individual will establish department-wide analytical strategies, drive late-stage analytical development, and provide technical leadership to ensure robust, phase-appropriate analytical control strategies and analytical methods. The Associate Director will also ensure phase-appropriate characterization of our products to ensure a growing state of knowledge leading all the way to a BLA filing. Working collaboratively with Analytical Project Leads and other functional leaders, the Associate Director will help integrate analytical activities across programs, strengthen technical capabilities, and prepare development programs for late-stage clinical development and eventual commercialization. This position serves as the senior scientific leader for Analytical Sciences and functions as a strategic partner to Analytical Project Leads and other functional experts. The role focuses on advancing analytical capabilities, enabling late-stage development, and ensuring scientific excellence across the portfolio while collaborating with program leaders responsible for day-to-day execution. This full-time, regular position will be located onsite in Durham, NC.

Summary of Key Responsibilities

Functional Leadership

  • Establish and evolve the Analytical Sciences strategy to support the company's growing development portfolio.
  • Develop best practices, scientific standards, and analytical governance across programs.
  • Identify opportunities to strengthen departmental capabilities, technologies, and external partnerships.
  • Mentor scientists and contribute to building a high-performing analytical organization.

Technical Leadership

  • Provide scientific leadership for analytical lifecycle management, comparability strategies, method validation, specification development, reference standard strategy, and control strategy development.
  • Guide analytical planning for late-stage clinical development, process validation, commercial readiness, and regulatory submissions.
  • Lead scientific evaluation of complex analytical challenges and recommend strategic solutions.

Cross-Program Collaboration

  • Partner with Analytical Project Leads to provide scientific consultation, establish department-wide analytical strategies, and promote consistency of analytical approaches across the development portfolio.
  • Collaborate with Cell Line Development, Upstream and Downstream Process Development, Formulation Development, Pilot Plant, Bioassay, Quality, Manufacturing, and Regulatory Affairs to ensure integrated CMC strategies.
  • Support portfolio planning by identifying cross-program opportunities, technical risks, and resource needs.
  • Support Quality in updating SOPs and procedures to be phase appropriate

External Scientific Leadership

  • Provide scientific oversight for external analytical laboratories and CROs.
  • Lead technical interactions with external partners and support due diligence, technology transfers, and regulatory inspections.
  • Evaluate emerging analytical technologies and recommend implementation where appropriate.
  • Lead investigations as necessary for out-of-trend / out-of-specification results

Required Qualifications

We are looking for professionals with the following required skills to achieve our goals:

  • Ph.D. in Chemical/Biochemical Engineering or related Biological Sciences with 6+ years of experience in the Pharmaceutical/Biotech analytical CMC industry, or B.S./M.S. in in Chemical/Biochemical Engineering or related Biological Sciences with 12 years of experience in the Pharmaceutical/Biotech industry analytical CMC industry
  • Demonstrated experience advancing biologic products through IND and clinical development
  • Experience leading multidisciplinary CMC teams in a matrix environment.
  • Experience managing CDMOs and external development partners
  • Strong understanding of CMC regulatory expectations for biologic products
  • Excellent communication, leadership, and project management skills

Preferred Qualifications

  • Experience supporting Phase 2/3 development, commercial readiness and BLA submissions
  • Experience with addressing regulatory questions from worldwide health authorities
  • Experience with technology transfer, comparability, process validation, and lifecycle management
  • Experience supporting due diligence and strategic partnerships with CROs as well as providing oversight to these companies
  • Experience working in a fast-paced biotechnology environment with multiple concurrent development programs