Bioanalytical Scientist

5AM Ventures; Emeryville (CA); On-site; USD 140,000 - 170,000; Full time

Benefits offered by this job

Performance bonuses

Equity participation

Comprehensive health benefits

Job summary

5AM Ventures located in Emeryville, California is seeking an experienced scientist to lead bioanalytical strategy and quality control for peptide, protein, and small molecule therapeutics.

The ideal candidate will have a PhD in Analytical Chemistry, 8-15 years of relevant experience, and expertise in method development. The role involves defining analytical approaches, leading CRO oversight, and ensuring data integrity.

Compensation ranges from $140,000 to $170,000 annually, with performance bonuses and comprehensive health benefits.

Qualifications

• 8–15+ years of relevant experience in biotech, pharma, or CRO environments.
• Demonstrated expertise in bioanalytical method development, validation, and data interpretation.
• Solid grounding in pharmacokinetics and interpretation of concentration–time data.

Responsibilities

• Define fit-for-purpose analytical approaches for PK, PD, and mechanistic studies.
• Design and manage outsourced bioanalytical studies.
• Evaluate calibration models, LLOQ, accuracy/precision, and assay robustness.
• Ensure methods and datasets meet GLP and regulatory expectations.
• Work closely with PK/PD, biology, and clinical teams to interpret data correctly.

Skills

Bioanalytical method development

Data interpretation

Analytical thinking

Quality control (QC)

Understanding of regulatory expectations

Pharmacokinetics

Education

PhD in Analytical Chemistry or related field

Job description

We are seeking an experienced, highly quantitative scientist to lead bioanalytical strategy and quality control across a diverse portfolio of peptide, protein, and small molecule therapeutics. This individual will define analytical approaches, oversee external CROs, and ensure that all data generated are accurate, reproducible, and decision-grade.

This role is ideal for someone who combines deep knowledge of bioanalytical methods with a strong QC mindset and the ability to diagnose and resolve complex analytical challenges across multiple assay platforms.

Qualifications

• PhD in Analytical Chemistry, Pharmaceutical Sciences, Biochemistry, or related field
• 8–15+ years of relevant experience in biotech, pharma, or CRO environments
• Demonstrated expertise in bioanalytical method development, validation, and data interpretation
• Strong understanding of both:
  • Ligand-binding assays (e.g., ELISA, MSD)
  • LC-MS/MS-based quantitation (hands-on experience not required, but deep conceptual understanding is essential)
• Experience overseeing and critically evaluating CRO-generated data
• Working knowledge of GLP bioanalysis and regulatory expectations (e.g., ICH M10)
• Solid grounding in pharmacokinetics and interpretation of concentration–time data

Preferred Qualifications

• Experience across multiple molecular modalities (peptides, monoclonal antibodies, small molecules)
• Background in analytical development or QC for regulated products
• Experience supporting IND-enabling studies or clinical programs
• Familiarity with complex or long-acting drug delivery systems

Responsibilities

• Own bioanalytical strategy
  • Define fit-for-purpose analytical approaches for PK, PD, and mechanistic studies
  • Select appropriate assay platforms (ligand-binding, LC-MS-based, hybrid methods)
• Lead CRO oversight
  • Design and manage outsourced bioanalytical studies
  • Critically review assay development, validation, and sample analysis
  • Identify deficiencies in methods, data quality, or interpretation and drive resolution
• Ensure quantitative rigor and data integrity
  • Evaluate calibration models, LLOQ, accuracy/precision, and assay robustness
  • Detect and troubleshoot issues such as matrix effects, instability, adsorption, and assay interference
  • Establish internal standards for data quality across programs
• Apply QC and regulatory principles
  • Ensure methods and datasets meet GLP and regulatory expectations (e.g., ICH M10)
  • Contribute to analytical sections of IND-enabling packages and regulatory filings
  • Implement quality systems and documentation standards where needed
• Support cross‑functional decision making
  • Work closely with PK/PD, biology, and clinical teams to interpret data correctly
  • Distinguish analytical artifacts from true biological signals
  • Provide clear recommendations based on quantitative evidence
• Operate across modalities
  • Apply consistent analytical thinking across peptides, biologics, and small molecules
  • Ensure comparability and continuity of data across platforms and studies

$140,000 - $170,000 a year

Final compensation will be based on a candidate’s qualifications, experience, and geographic location. Employees are also eligible for performance bonuses, equity participation and comprehensive health benefits.

We believe in building balanced teams. We are an equal opportunity employer. We do not discriminate in regard to race, color, religion, national origin, age, sex, sexual orientation, gender identity, marital status, ancestry, physical or mental disability, veteran status, or any other legally protected characteristics.