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Associate Director Pharmaceutical Jobs (NOW HIRING)

AstraZeneca

Associate Director, CMC Lead

Boston, MA

$136K - $204K/yr

Associate Director, CMC Lead Introduction to role: Are you ready to lead early-stage CMC strategy ... Define and deliver the pharmaceutical development strategy for the pre-IND/IND-enabling portfolio ...

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Coastal Equities, Inc.

Associate Director (HLS)

The Associate Director is responsible for overseeing the customer experience across a dedicated portfolio of HLS clients-spanning healthcare providers, payers, pharmaceuticals, and medical device ...

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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
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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 Scientific Communications

Zentalis Pharmaceuticals

San Diego, CA • On-site

$180K - $220K/yr

Full-time

Posted 21 days ago

Job description

ASSOCIATE DIRECTOR SCIENTIFIC COMMUNICATIONS
Zentalis is a clinical oncology innovator developing a treatment approach for ovarian cancer and multiple tumor types. Leveraging therapeutics development and biomarker expertise, Zentalis is advancing monotherapy and combination studies of its investigational first-in-class WEE1 inhibitor, azenosertib. Focused on translating WEE1 science into clinical practice, we aim to equip physicians with a targeted, non-chemo, orally available medicine that enhances treatment experience, choice, and outcomes. Our mission: to unburden cancer patients with more convenience and care.
POSITION SUMMARY:
The Associate Director Scientific Communications will be a key member of the Medical Affairs team. This key role will play a pivotal role in translating complex data into clear, credible, and impactful scientific evidence and narratives that shape how Zentalis treatment approach for ovarian cancer and multiple tumor types is understood and applied across the global medical community. Operating at the intersection of strategy and execution, this role partners closely with cross-functional colleagues and external experts to deliver high-impact publications and scientific communications that advance both patient care and scientific dialogue. This is a unique opportunity to join a highly collaborative, mission-driven team known for scientific excellence, thoughtful partnership, and getting meaningful data to the audiences who need it most.
ESSENTIAL DUTIES AND RESPONSIBILITIES:
  • Contribute to the development of global strategic publication and scientific communications plans in alignment with the overall corporate strategy
  • Manage the planning and execution of publication tactics (manuscripts, abstracts, posters, oral presentations etc.) in accordance with GPP3, ICMJE, and Zentalis policies
  • Ensure the development and dissemination of scientific, clinical, and health-related information to healthcare professionals, patients, payers, regulators, and other stakeholders (Medical Information/MedComms)
  • Facilitate and operationalize the publication review process at Zentalis
  • Facilitate discussions/decisions at regular publication team meetings related to publication planning and execution
  • Develop and/or update scientific platforms
  • Manage and execute the development of scientific communication tactics, FAQs, medical tools, and congress materials
  • Partner with internal and external SMEs to develop credible, accurate, and impactful scientific content
  • Ensure materials progress efficiently through medical and publication review committees
  • Manage scientific communication and publication vendors, as well as electronic publication management systems
  • Identify opportunities to proactively address clinical and scientific knowledge gaps
  • Build and maintain disease-area expertise through continuous review of the scientific literature
  • Development of scientific training tactics (eg, internal training MSL decks, tools, FAQs).

KNOWLEDGE/SKILLS/ABILITIES REQUIRED:
  • Advanced degree with 5-7+ yrs. experience in scientific communication, training, publications planning and development in an agency or pharmaceutical environment or applicable experience working in pharmaceutical environment with transferable skill set.
  • Prior hands-on experience in medical information & communications for a pharmaceutical company is required.
  • Demonstrated ability to work with cross-functional teams and/or agencies to develop abstracts, posters, oral presentations, manuscripts, slide decks, and content for scientific and educational programs
  • Strong project management skills and leadership poise to negotiate and facilitate alignment amongst internal and external stakeholders (KOLs, authors, cross-functional teams)
  • Proven ability to be well organized, multi-task, and manage vendors, timelines, and competing priorities in a fast-paced, deadline-driven environment
  • Excellent and effective interpersonal and communication skills
  • Strong understanding of publication compliance standards (GPP3, ICMJE, FDA/OIG guidance, MALR)
  • Willingness to travel (U.S. and international) ~20%

Apply