Position: Associate Director, Antibody-Drug Conjugates (ADC)
Location: Alameda, CA
Reports To: Senior Director of R&D
Employment Type: Full-Time, on-site
Job Description:
We are seeking a highly motivated Associate Director, Antibody-Drug Conjugates (ADC) to play a key role in our ADC and related development programs. The ideal candidate will have a strong background in conjugation chemistry and linker-payload development/optimization, with a proven track record of leading successful ADC programs from discovery to IND submission. This role requires exceptional leadership and communication skills and will collaborate effectively with internal and external stakeholders, driving innovative solutions to advance our ADC technology.
Key Responsibilities:
- Provide scientific leadership and expertise in the execution of ADC pipelines, including chemistry/bio-conjugation design, linker-payload design, conjugation process development, and preclinical study design.
- Manage project timelines, budgets, and resources to ensure alignment with corporate goals and timely delivery of milestones.
- Prepare high-quality scientific documents, including peer-reviewed publications, regulatory submissions (e.g., IND), study reports, and presentations.
- Collaborate with internal teams, including clinical, regulatory, and manufacturing, to integrate ADC development efforts seamlessly.
- Partner with external CROs for ADC manufacturing and scale-up processes.
- Analyze and interpret experimental data, providing actionable insights to internal and external stakeholders.
- Support due diligence and integration of external assets into the company's pipelines.
- May supervise and mentor junior scientists and research associates.
Required Qualifications:
Education:
- Ph.D. in life sciences (oncology, immunology, chemistry, medicine, or related field) with a minimum of 8 years of industry experience, OR
- BS/MS with at least 12 years of industry experience in ADC development.
Experience:
- Proven expertise in linker/payload design, ADC pipeline development, including preclinical, pharmacokinetic, and pharmacodynamic studies.
- Hands-on experience with IND preparation and regulatory filings (e.g., IND, BLA).
- Strong background in bioconjugation chemistry and analytical methods (e.g., LC-MS, HPLC, SEC).
- Familiarity with CMC processes, including manufacturing and scale-up for biologics.
- Excellent scientific writing, including publications and regulatory documents.
- Strong interpersonal and communication skills with experience working in cross-functional teams.
- Demonstrated ability to manage multiple projects simultaneously and deliver results within deadlines.
