Director, Bioanalytical Strategy (Remote/Hybrid)

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

Benefits offered by this job

Flexible work environment

Job summary

Disc Medicine, Inc. is seeking an Associate Director/Director, Bioanalytical to lead and oversee bioanalytical activities across preclinical and clinical programs.

The role includes assay development, validation, and data review, with collaboration across discovery, nonclinical, clinical, DMPK, and CRO partners. The candidate will act as SME for bioanalytical sciences, drive regulatory submissions, and manage timelines, budgets, and vendor deliverables while maintaining hands-on involvement in

Qualifications

• Ph.D. in a relevant scientific discipline with 8+ years of industry experience in bioanalysis.
• Experience supporting GLP toxicology and clinical studies with regulatory guidance.
• Expertise in LC-MS/MS, ligand-binding assays, and cell-based assays.
• Hands-on experience with cell-based assays and flow cytometry preferred.
• Experience with biomarker and/or pharmacodynamic analysis is desirable.
• Strong communication and collaboration across cross-functional teams.

Responsibilities

• Lead bioanalytical activities including assay development, validation, sample analysis, data review and reporting.
• Serve as bioanalytical project lead and strategic partner to internal teams.
• Collaborate with CROs for method development, validation, and troubleshooting.
• Oversee timelines, data quality, resources, and vendor deliverables.
• Act as SME for bioanalytical sciences and contribute to regulatory submissions.

Skills

Bioanalysis

LC-MS/MS

Regulatory knowledge

Data review

Project leadership

Education

Ph.D. in a relevant scientific discipline

Tools

Flow cytometry

NAb assays

Biomarker assays

Job description

Disc Medicine, Inc. is seeking an Associate Director/Director, Bioanalytical to lead and oversee bioanalytical activities across preclinical and clinical programs.

The role includes assay development, validation, and data review, with collaboration across discovery, nonclinical, clinical, DMPK, and CRO partners. The candidate will act as SME for bioanalytical sciences, drive regulatory submissions, and manage timelines, budgets, and vendor deliverables while maintaining hands-on involvement in