Senior Director, Bioanalytical – Remote/Hybrid

Disc Medicine; Massachusetts; Hybrid; USD 187,000 - 228,000; Full time

Job summary

Disc Medicine seeks an Associate Director/Director, Bioanalytical to provide technical and operational support for bioanalytical activities across drug development programs. You will oversee outsourced studies in GLP/GCP and non-GLP environments, collaborating with discovery, nonclinical, clinical, DMPK, and CRO partners to ensure high-quality PK, ADA, and biomarker analyses.

The role requires a Ph.D. with 8+ years in regulated bioanalysis, hands-on assay development/validation, and strong

Qualifications

• Ph.D. in a scientific discipline with 8+ years of industry bioanalysis experience.
• Hands-on GLP toxicology and clinical study support experience.
• Expertise in bioanalytical assay development and validation (LC-MS/MS, ligand-binding, cell-based).
• Experience managing CROs/external vendors and regulatory interactions.

Responsibilities

• Lead bioanalytical activities including assay development, validation, sample analysis, data review and reporting.
• Serve as a bioanalytical project lead and partner to internal cross-functional teams.
• Collaborate with CROs and labs to develop and execute strategies (development, validation, analysis).
• Oversee timelines, data quality, budgeting, and vendor deliverables.
• Act as SME for bioanalytical sciences within Disc Medicine.
• Contribute to regulatory submissions and responses.

Skills

Bioanalytical project leadership

Regulatory communications

Cross-functional collaboration

Education

Ph.D. in a relevant scientific discipline

Tools

LC-MS/MS

Ligand-binding assays

Cell-based assays

Flow cytometry

NAb assays

Job description

Disc Medicine seeks an Associate Director/Director, Bioanalytical to provide technical and operational support for bioanalytical activities across drug development programs. You will oversee outsourced studies in GLP/GCP and non-GLP environments, collaborating with discovery, nonclinical, clinical, DMPK, and CRO partners to ensure high-quality PK, ADA, and biomarker analyses.

The role requires a Ph.D. with 8+ years in regulated bioanalysis, hands-on assay development/validation, and strong