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Associate Director Analytical Development Jobs (NOW HIRING)

Rocket Pharmaceuticals

NJ · On-site

$220 - $293/hr

Position Summary Rocket Pharma is seeking an experienced Senior Director, Analytical Development to join our Technical Development team. Reporting to the Vice President, Technical Development, the ...

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Associate Director Analytical Development information

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$93.3K

$180K

How much do associate director analytical development jobs pay per year?

As of Sep 7, 2026, the average yearly pay for associate director analytical development in the United States is $93,350.00, according to ZipRecruiter salary data. Most workers in this role earn between $72,500.00 and $103,000.00 per year, depending on experience, location, and employer.

What does an associate director analytical development do?

An Associate Director of Analytical Development is responsible for overseeing the development, validation, and implementation of analytical methods used to test pharmaceutical products or biologics. They lead teams of scientists, manage laboratory operations, and ensure compliance with regulatory requirements. Their role is crucial in supporting product development, quality control, and ensuring the safety and efficacy of drugs throughout the development process.

What are the key skills and qualifications needed to thrive as an associate director analytical development, and why are they important?

To thrive as an Associate Director Analytical Development, you need a strong background in analytical chemistry, method development, and pharmaceutical regulations, typically supported by an advanced degree in a relevant scientific field. Familiarity with analytical instruments such as HPLC, GC, and mass spectrometry, as well as experience with regulatory submission systems and quality management tools, is crucial. Leadership, strategic thinking, and effective communication are vital soft skills for managing teams and collaborating cross-functionally. These skills ensure robust analytical support for drug development, regulatory compliance, and successful project delivery.

What are some common challenges faced by an associate director analytical development, and how can they be addressed?

An Associate Director of Analytical Development often encounters challenges such as managing multiple complex projects simultaneously, ensuring regulatory compliance, and fostering effective collaboration between cross-functional teams. Balancing the need for robust scientific methods with tight project timelines requires strong organizational and leadership skills. To address these challenges, it is essential to establish clear communication channels, prioritize tasks based on risk and impact, and stay updated on evolving regulatory guidelines. Actively mentoring team members and promoting a culture of continuous improvement can also help streamline workflows and enhance overall team performance.

What is the difference between Associate Director Analytical Development vs Senior Scientist Analytical Development?

AspectAssociate Director Analytical DevelopmentSenior Scientist Analytical Development
ResponsibilitiesOversees analytical development teams, manages project strategies, and ensures regulatory compliance.Conducts experimental work, develops assays, and supports project execution under supervision.
Required CredentialsBachelor's or Master's in Chemistry, Biochemistry, or related; 8+ years experience; leadership skills.Bachelor's or Master's in relevant field; 5+ years experience; technical expertise.
Work EnvironmentLeads teams in R&D or manufacturing settings, often in biotech or pharma companies.Performs laboratory research, assay development, and experimental analysis.

The main difference is that the Associate Director Analytical Development holds leadership and strategic responsibilities, overseeing teams and projects, while the Senior Scientist Analytical Development focuses on hands-on experimental work and technical development. Both roles require strong scientific credentials and industry experience, but the associate director position involves more managerial duties and project oversight.

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Associate Director Analytical Development jobs near you
Infographic showing various Associate Director Analytical Development job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 82% Full Time, 15% Part Time, and 2% Contract. Highlights an 91% Physical, 3% Hybrid, and 6% Remote job distribution, with an average salary of $93,350 per year, or $44.9 per hour.

Associate Director, Analytical Development & CMC Statistics

Summit Therapeutics

Princeton, NJ • On-site

Full-time

Posted 13 days ago

Key responsibilities

  • Provide scientific and technical leadership for analytical method development, qualification, validation, transfer, troubleshooting, and lifecycle management for biologic drug substance and drug product programs.

  • Support phase-appropriate analytical strategies for release, stability, characterization, comparability, potency, binding, impurity, and residual testing.

  • Lead statistical planning, analysis, and interpretation for analytical method validation, method transfer, comparability, stability, specification setting, assay qualification, and investigation support.

Job description

About Summit:
Summit Therapeutics Inc. is a biopharmaceutical oncology company with a mission focused on improving quality of life, increasing potential duration of life, and resolving serious unmet medical needs. At Summit, we believe in building a team of world class professionals who are passionate about this mission, and it is our people who drive this mission to reality. Summit's core values include integrity, passion for excellence, purposeful urgency, collaboration, and our commitment to people. Our employees are truly the heart and soul of our culture, and they are invaluable in shaping our journey toward excellence.
Summit's team is inspired to touch and help change lives through Summit's clinical studies in the field of oncology. Summit has multiple global Phase 3 clinical studies, including:
Non-small Cell Lung Cancer (NSCLC)
  • HARMONi: Phase 3 clinical study which was intended to evaluate ivonescimab combined with chemotherapy compared to placebo plus chemotherapy in patients with EGFR-mutated, locally advanced or metastatic non-squamous NSCLC who were previously treated with a 3rd generation EGFR TKI.
  • HARMONi-3: Phase 3 clinical study which is intended to evaluate ivonescimab combined with chemotherapy compared to pembrolizumab combined with chemotherapy in patients with first-line metastatic NSCLC.
  • HARMONi-7: Phase 3 clinical study which is intended to evaluate ivonescimab monotherapy compared to pembrolizumab monotherapy in patients with first-line metastatic NSCLC.

Colorectal Cancer (CRC)
  • HARMONi-GI3: Phase 3 clinical study intended to evaluate ivonescimab in combination with chemotherapy compared with bevacizumab plus chemotherapy.

Ivonescimab is an investigational therapy not presently approved by any regulatory authority other than China's National Medical Products Administration (NMPA). Summit is headquartered in Miami, Florida, and has additional offices in California, New Jersey, the UK, and Ireland.
Overview of Role:
The Associate Director of Analytical Development and CMC Statistics will provide technical and statistical leadership for analytical development, method validation, method transfer, comparability, stability, specifications, and lifecycle management activities supporting biologic drug substance and drug product programs. This role will sit within the CMC Analytical Sciences organization and will partner closely with Analytical, MSAT, Quality, Regulatory Affairs, Supply Chain, and external CDMOs/CROs to ensure that analytical strategies, statistical approaches, and data packages are scientifically robust, phase-appropriate, compliant, and suitable for global regulatory submissions and commercial readiness.
The successful candidate will combine hands-on experience in biologics analytical development with strong statistical expertise, including method validation statistics, stability and shelf-life modeling, specification setting, comparability assessments, assay lifecycle monitoring, and statistical support for CMC investigations. This individual will be expected to translate complex analytical datasets into clear conclusions, support risk-based decision-making, and contribute directly to IND/IMPD, BLA/MAA, post-approval, and health authority response activities.
Role and Responsibilities:
  • Provide scientific and technical leadership for analytical method development, qualification, validation, transfer, troubleshooting, and lifecycle management for biologic drug substance and drug product programs.
  • Support phase-appropriate analytical strategies for release, stability, characterization, comparability, potency, binding, impurity, and residual testing.
  • Review and interpret analytical data from CDMOs, CROs, and partner laboratories to ensure methods are robust, fit for purpose, and aligned with regulatory expectations.
  • Contribute to analytical control strategy development, including critical quality attribute assessment, method performance monitoring, and product quality trend evaluation.
  • Lead statistical planning, analysis, and interpretation for analytical method validation, method transfer, comparability, stability, specification setting, assay qualification, and investigation support.
  • Apply appropriate statistical tools to evaluate accuracy, precision, linearity, range, robustness, intermediate precision, equivalence, trending, outliers, assay variability, and method capability.
  • Develop and justify statistically sound acceptance criteria, comparability criteria, stability models, DS and DP shelf-life determinations, stability trending approaches, and analytical control limits.
  • Partner with CMC, Quality, Regulatory Affairs, and external partners to ensure statistical approaches are scientifically defensible and clearly documented in protocols, reports, and regulatory submissions.
  • Support data visualization, multivariate analysis, and trend monitoring to enable early identification of analytical or manufacturing risks.
  • Support inspection readiness, audit responses, regulatory commitments, and post-approval lifecycle management activities related to analytical methods, stability, specifications, and comparability.
  • Provide statistical input into deviations, OOS/OOT investigations, CAPAs, change controls, and risk assessments.
  • Provide analytical and statistical oversight for external CDMOs, CROs, and partner laboratories performing release, stability, characterization, method transfer, method validation, and comparability studies.
  • Review external protocols, reports, data packages, deviations, and investigations to ensure technical quality, compliance, and alignment with program objectives.
  • Communicate complex analytical and statistical findings clearly to technical and non-technical stakeholders, including senior leadership.
  • Contribute to internal SOPs, templates, best practices, and governance processes for analytical development, CMC statistics, and outsourced analytical activities.
  • All other duties as assigned.

Experience, Education and Specialized Knowledge and Skills:
  • Advanced degree(s) preferred in Statistics, Biostatistics, Analytical Chemistry, Biochemistry, Pharmaceutical Sciences, Chemical Engineering, or a related scientific discipline; Bachelor's or master's degree with substantial relevant experience will be considered.
  • Minimum of 10+ years of relevant experience in the biopharmaceutical or pharmaceutical industry, including direct experience supporting CMC analytical development and/or process development and manufacturing activities.
  • Strong knowledge and understanding of biologics analytical methods, including chromatographic, electrophoretic, immunoassay, potency, binding, impurity, and/or process residuals.
  • Demonstrated experience with analytical method development, validation, method transfer, comparability, specification setting, stability analysis, and statistical analysis & interpretation of CMC datasets.
  • Working knowledge of ICH, FDA and EMA guidance and GMP regulation, as well as data integrity expectations relevant to analytical development and lifecycle management.
  • Experience reviewing or authoring protocols, reports, regulatory submission sections, health authority responses, deviations, OOS/OOT investigations, CAPAs, and change controls.
  • Travel may be required periodically to support CDMO/CRO oversight, technical meetings, regulatory interactions, or cross-functional workshops.

This is the pay for this position
Pay Transparency
$180,000-$200,000 USD
Actual compensation packages are based on several factors that are unique to each candidate, including but not limited to skill set, depth of experience, certifications, and specific work location. This may be different in other locations due to differences in the cost of labor. The total compensation package for this position may also include bonus, stock, benefits and/or other applicable variable compensation.
Summit does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact Summit's Talent Acquisition team at recruiting@smmttx.com to obtain prior written authorization before referring any candidates to Summit.
Summit Therapeutics Inc. is an Equal Opportunity Employer and takes pride in creating and maintaining diverse environment. We do not discriminate in recruitment, hiring, training or promotion or any other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, marital or veteran status, disability, or any other legally protected status.

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