Syndax Pharmaceuticals

Director/Senior Director, Bioanalysis

Syndax Pharmaceuticals$250K — $300K *
Pharmaceuticals & Biotech
8 - 10 years of experience
Job Overview by Ladders

Qualifications

  • PhD or MS in Analytical Chemistry, Biochemistry, Pharmaceutical Sciences, or related discipline.
  • 10+ years of experience for PhD holders, 15+ years for MS holders in the biotech/pharmaceutical industry.
  • Deep expertise in bioanalysis with knowledge of GLP regulations and pharmacokinetic principles.
  • Experience authoring regulatory submissions and related documentation.
  • Proven strategic leadership and influencing skills in cross-functional teams.
  • Excellent organization, project management, and communication skills.

Responsibilities

  • Define and execute bioanalytical strategies for small molecules and biologics in development.
  • Serve as the internal expert on bioanalytical methods and technologies.
  • Oversee assay development, validation, and analysis to ensure high-quality results.
  • Drive selection and performance management of contract research organizations (CROs).
  • Review and approve bioanalytical protocols and regulatory documents.
  • Collaborate with various functions to meet project milestones.
  • Establish best practices and drive continuous improvement in bioanalytical processes.

Benefits

  • Opportunity to lead and shape the future of bioanalysis at Syndax.
  • Access to a competitive benefits program including health and wellness.
  • Participation in an equity offering for long-term incentive.
  • Potential for annual target bonuses based on performance.
  • Supportive culture focusing on mentorship and professional growth.
Full Job Description
Director/Senior Director, Bioanalysis

The Role:

Syndax is seeking a strategic and experienced bioanalytical leader to oversee bioanalytical activities across our development portfolio. Reporting to the Head of Clinical Pharmacology, this individual will lead and execute bioanalytical strategies for both small molecules and biologics, supporting nonclinical and clinical development programs. For Senior Director candidates, the role also includes organizational leadership and people management responsibilities. This is a unique opportunity to make a significant impact on the development of innovative therapies while shaping the capabilities, strategy, and future growth of the Bioanalysis function at Syndax.

Key Responsibilities:
  • Define and execute end-to-end bioanalytical strategies for small molecules and biologics supporting nonclinical and clinical development programs across the portfolio.
  • Serve as the internal subject matter expert in bioanalysis, including LC-MS/MS, ligand-binding assays, immunogenicity, biomarker assays, and novel analytical technologies.
  • Oversee assay development, validation, and sample analysis activities at CROs, ensuring scientific rigor, regulatory compliance, and timely delivery of high-quality results.
  • Drive CRO selection, oversight, and performance management while providing scientific leadership to resolve complex technical and operational challenges.
  • Review and approve bioanalytical protocols, validation reports, sample analysis reports, and regulatory submission documents.
  • Partner cross-functionally with Clinical Pharmacology, DMPK, Clinical Development, Clinical Operations, Translational Medicine, Regulatory Affairs, and Quality Assurance to support program milestones.
  • Represent Bioanalysis on project teams, regulatory interactions, due diligence activities, and strategic development initiatives.
  • Establish and maintain bioanalytical best practices, driving continuous improvement in assay development, sample management, vendor oversight, and operational processes.
  • Stay current with advances in bioanalytical science, regulatory guidance, and industry best practices, incorporating innovative approaches when appropriate.

Additional Responsibilities (Senior Director)
  • Provide organizational leadership and strategic direction for the Bioanalysis function across the portfolio.
  • Build, lead and mentor bioanalytical scientists while fostering a culture of accountability, collaboration, innovation, and scientific excellence.
  • Drive long-term resource planning, budget management, and external partnership strategies.


Desired Experience/Education and Personal Attributes:

Education
  • PhD or MS in Analytical Chemistry, Biochemistry, Pharmaceutical Sciences, or a related scientific discipline.

Director Qualifications
  • PhD or MS in Analytical Chemistry, Biochemistry, Pharmaceutical Sciences, or a related scientific discipline.
  • PhD with 10+ years, or MS with 15+ years, of relevant pharmaceutical or biotechnology industry experience.
  • Deep expertise in bioanalysis, including mass spectrometry, ligand-binding assays, and biologics, with a strong understanding of GLP regulations, regulatory guidance, and pharmacokinetic principles.
  • Demonstrated experience authoring and reviewing regulatory submissions, health authority responses, SOPs, validation documentation, and due diligence assessments.
  • Proven track record of providing strategic scientific leadership and influencing cross-functional teams to achieve development objectives.
  • Sound scientific judgment with a proven ability to identify, troubleshoot, and resolve complex technical and operational challenges.
  • Excellent collaboration and stakeholder management skills, with experience working effectively across internal functions and external partners.
  • Outstanding communication and presentation skills, with the ability to convey complex scientific concepts to diverse audiences.
  • Highly organized and results-oriented, with strong project management skills and the ability to manage multiple priorities in a dynamic environment.

Additional Qualifications (Senior Director)
  • PhD with 15+ years, or MS with 20+ years, of relevant pharmaceutical or biotechnology industry experience for Senior Director level.
  • Proven leadership experience, including mentoring bioanalytical scientists, talent development and performance management.
  • Demonstrated ability to develop organizational capabilities, empower teams, and build a culture of accountability and excellence.


Location: Syndax's corporate office is in New York, NY.

Syndax offers a total compensation and rewards package that is among the most competitive in the industry. Base pay is just one element of our package and is determined within a range based on several factors including market data, experience, qualifications, demonstrated skills, relevant education or training, travel requirements and internal equity. Our overall package also includes an equity offering, annual target bonuses, and an outstanding benefits program. The anticipated annualized salary range for this role is $250,000 - $300,000.

#LI-Remote

About Syndax Pharmaceuticals

Syndax Pharmaceuticals is a clinical-stage biopharmaceutical company developing an innovative pipeline of cancer therapies. The company's lead product candidate, entinostat, is a selective HDAC inhibitor that has been evaluated in multiple clinical trials in combination with immune checkpoint inhibitors and targeted therapies. Syndax is also developing SNDX-5613, a highly selective and potent inhibitor of the Menin-MLL interaction, for the treatment of acute leukemias. The company is committed to improving the lives of cancer patients through the discovery and development of novel therapies.
Learn more about Syndax Pharmaceuticals
Size
59 employees
Market Cap
$1.6 billion
Industry
Net Income
-$73.1 million
Founded
2005
5 Year Trend
+158.1%
Revenue
$1.5 million
NASDAQ

Similar Jobs

More Jobs at Syndax Pharmaceuticals

More Pharmaceuticals & Biotech Jobs

Find similar Director/Senior Director, Bioanalysis jobs: