Kailera Therapeutics - Hybrid work

Lead global clinical and commercial drug supply strategy in Waltham. This director role requires 8+ years of clinical supply management expertise, including IRT systems and CDMO oversight. Enjoy comprehensive benefits, bonus potential, and equity in a collaborative, fast-paced biopharma environment.

Lead Analytical Development and QC for innovative drug programs from clinical to commercial stages. Oversee GMP release, stability, and data integrity at CDMOs for injectable and oral dosage forms. Utilize advanced analytical techniques and stability software in a key CMC role. Based in Waltham w...

Lead global clinical supply chain operations for a biopharma leader in Waltham. Utilize your 10+ years of experience in clinical supply management and IRT systems to ensure uninterrupted investigational product supply. This hands-on role offers comprehensive benefits, bonus potential, and equity ...

Lead CMC Operations for pharmaceutical development projects in Waltham. Manage CDMO alliances, tech transfers, manufacturing, and regulatory submissions with 10+ years of industry experience. Enjoy comprehensive benefits, flexible time off, and equity in a collaborative, cross-functional environm...

Seeking an experienced Medical Director for Clinical Development in Waltham. Lead clinical strategy and trial execution for innovative therapeutics in a dynamic biotech environment. An MD with 3+ years of industry experience in clinical development and trial design is required. We offer comprehen...

Gain hands-on medical communications experience in Waltham, contributing to publications, slide decks, and congress planning. Collaborate cross-functionally and lead a project to develop leadership skills. Ideal for a bachelor's candidate with strong communication skills and scientific coursework...

Lead global CMC regulatory strategy for drug development and commercialization in this director-level role. Based in Waltham, you will manage submissions, ensure compliance, and provide strategic guidance. The position requires 10+ years of CMC experience and offers comprehensive benefits, bonus ...

Lead the scientific execution of Phase I-III trials as a hands-on Director, Clinical Scientist. Partner with Clinical Operations to ensure high-quality trial conduct, rigorous data review, and clear communication. This senior role in Waltham requires 8+ years of experience and offers comprehensiv...

Seeking an Associate Director of Clinical QA in Waltham, MA. This hands-on GCP/GVP expert will lead risk-based quality management, audit programs, and inspection readiness for clinical studies. Requires 10+ years in FDA-regulated industry with Veeva suite proficiency. Enjoy comprehensive benefits...

Lead non-clinical safety strategy as a Senior Director of Toxicology in Waltham. Utilize your 10+ years of expertise and regulatory success with INDs/NDAs to guide complex programs. This strategic role offers comprehensive benefits, bonus potential, and equity while ensuring scientific and operat...

Lead pharmacovigilance quality and compliance for a global biotech in Waltham. This senior role requires 8+ years of PV experience, expertise in global regulations (FDA, EMA, ICH), and a strong background in audits and quality systems. Enjoy comprehensive benefits, flexible time off, and equity i...

Join our team in Waltham as a Manager of Patient Safety and Pharmacovigilance Operations. You will oversee safety vendor activities, ensuring compliance with global PV regulations and quality standards. This role requires 6+ years of PV Ops experience, Argus database proficiency, and vendor manag...