Sustainability Associate or Associate Director United States, Waltham Jobs

Lead global pharmacovigilance and safety surveillance for assigned products in this Waltham-based role. Utilize your 10+ years of PV experience in signal management, benefit-risk assessment, and aggregate reporting. Enjoy comprehensive benefits, flexible time off, and a collaborative, cross-funct...

Lead Alliance Management Operations at a dynamic biotech firm in Waltham. Utilize your 8+ years of life sciences experience to implement systems, create dashboards, and optimize strategic partnerships. This role offers comprehensive benefits, equity, and the chance to drive insight-driven decisio...

Lead global clinical supply chain operations to ensure uninterrupted investigational product delivery for trials. This role requires 6+ years of clinical supply management experience, IRT system expertise, and a collaborative, results-driven approach. Based in Waltham, MA or San Diego, CA, it off...

Join Kailera's growing Pharmacovigilance team as an Associate Director. You will oversee global PV operations, ensuring compliance with FDA, EMA, and ICH guidelines. This role, based in Waltham, MA or San Diego, CA, offers comprehensive benefits, bonus opportunities, and equity. Utilize your 10+ ...

Lead strategic pharmacovigilance planning and drive innovation in this key Associate Director role. You will manage global PV projects, optimize processes, and integrate new technologies from concept to adoption. The position requires 10+ years in pharmacovigilance and strong project management s...

Lead statistical programming for late-phase clinical trials and regulatory submissions in Waltham. This role requires 7+ years of SAS/CDISC expertise and experience overseeing CROs. We offer comprehensive benefits, bonus opportunities, and equity in a supportive environment.

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...

Seeking an Associate Director of Clinical Quality Assurance in Waltham, MA. This hands-on role requires a GCP/GVP expert with 10+ years' experience, including Veeva systems, to ensure compliance and inspection readiness. You will implement risk-based quality management and collaborate across clin...

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...

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 statistical programming for late-phase clinical trials and regulatory submissions in this Associate Director role. Oversee CROs and ensure CDISC-compliant SDTM/ADaM datasets. Leverage your 7+ years of SAS expertise in a collaborative Waltham-based team with comprehensive benefits and bonus p...

Seeking an experienced Associate Director for Analytical Development and QC in Waltham. Lead analytical strategy for drug substances/products from clinical development to commercialization. Requires 10+ years in pharma/biotech, with deep expertise in HPLC, stability programs, and CMC regulatory f...