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Associate Director Pharmaceutical Jobs (NOW HIRING)

Real Chemistry

Associate Director, Programmatic

... pharmaceutical and biotech industries. Our #LifeatRealChem culture is rooted in our people-we ... The Associate Director should be comfortable operating independently, managing priorities ...

Lonza

Associate Director, MSAT

Walkersville, MD · On-site +1

$174K - $203K/yr

Associate Director, MSAT Location: This position is currently remote. A future transition to an on ... Master's degree in engineering, Biotechnology, Pharmaceutical Sciences, Chemistry, Life Sciences ...

Lonza

Associate Director, MSAT

Walkersville, MD

$174K - $203K/yr

Associate Director, MSAT Location: This position is currently remote. A future transition to an on ... Master's degree in engineering, Biotechnology, Pharmaceutical Sciences, Chemistry, Life Sciences ...

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How much do associate director pharmaceutical jobs pay per year?

As of Aug 6, 2026, the average yearly pay for associate director pharmaceutical in the United States is $164,797.00, according to ZipRecruiter salary data. Most workers in this role earn between $121,500.00 and $200,000.00 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.

More about Associate Director Pharmaceutical jobs
What cities are hiring for Associate Director Pharmaceutical jobs? Cities with the most Associate Director Pharmaceutical job openings:
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Associate Director Pharmaceutical jobs near you
Infographic showing various Associate Director Pharmaceutical job openings in the United States 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 $164,797 per year, or $79.2 per hour.

Associate Director, Regulatory Affairs CMC

Skyhawk Therapeutics

Waltham, MA • On-site

$170K - $230K/yr

Other

Posted 28 days ago

Job description

Associate Director, Regulatory Affairs CMC

Skyhawk Therapeutics is seeking a hands-on, Associate Director, Regulatory Affairs CMC (RegCMC) to support the development and execution of the global RegCMC strategy for Skyhawk's small molecule pipeline. Working closely with the Director, RegCMC, you will help serve as a RegCMC point of contact across the organization, partnering with Pharmaceutical Development, Manufacturing, Quality, and Program teams to deliver high-quality, timely regulatory submissions that advance clinical development and support eventual commercialization. This is an ideal opportunity for a growing RegCMC professional who thrives in fast-paced, science-driven biotech where their work has direct and visible impact.

Responsibilities:

  • Support the development and execution of global RegCMC strategies for small-molecule programs across stages of development, from IND through NDA/MAA readiness.
  • Identify and work in collaboration with CMC Team to address regulatory risks.
  • Monitor evolving global health authority expectations and guidance (FDA, EMA, ICH) and translate them into actionable strategy.
  • Author and review all applicable Quality sections for global regulatory filings, including IND/IMPD, annual reports, and briefing documents.
  • Support and coordinate responses to CMC information requests with accuracy and timeliness.
  • Partner with Pharmaceutical Development, Manufacturing, Quality, and Program Management to provide regulatory input on control strategy, specifications, manufacturing changes, comparability, process validation, and lifecycle management.
  • Assist with CDMO and external partner oversight from a regulatory perspective, ensuring alignment with submission commitments.

Education/Skills/Experience Requirements:

  • Advanced degree (MS, PhD, PharmD) in chemistry, pharmaceutical sciences, chemical engineering, or a related discipline; a Bachelor's degree with directly relevant experience will be considered.
  • 7+ years of combined Regulatory Affairs CMC and pharmaceutical industry experience.
  • Experience contributing to global CMC regulatory strategy for small-molecule programs across one or more stages of development.
  • Hands-on authorship of CTD Module 3 content; working familiarity with ICH guidelines and applicable FDA/EMA guidance.
  • Experience supporting IND, NDA, or MAA regulatory submissions.
  • Ability to work both independently and collaboratively, and to prioritize in a fast-paced biotech environment.
  • Strong written and verbal communication skills.

Preferred Qualifications

  • Experience supporting a program through later-stage development or the clinical-to-commercial transition.
  • Exposure to both early- and late-stage pipeline assets within the same organization.

Skyhawk Therapeutics is committed to pay transparency and equitable compensation practices. The base salary range for the Associate Director, Regulatory Affairs CMC is $170,000-230,000 annually. This range reflects the minimum and maximum target for such position. Skyhawk Therapeutics will assess the appropriate level for a qualified candidate based on job-related skills, professional experience, and relevant education or training.

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