Associate Director, Research Strategic Planning And Operation-Project Management Vir Biotechnology, Inc.Associate Director, Research Strategic Planning And Operation-Project ManagementSan Francisco, CA$162,500–$227,500 / yearThe successful candidate will be a highly collaborative, proactive, and independent leader with strong scientific acumen, excellent communication skills, and demonstrated experience managing complex cross-functional programs in biotechnology or pharmaceutical research environments. Ability balance tactical execution and strategic leadership, from managing project plans, timelines, and meeting logistics to driving cross-functional alignment and facilitating strategic decision-making across all stages of development and levels of leadership.
Associate Director, Innovation AbbVie, IncAssociate Director, InnovationSouth San Francisco, CAResponsibilities: Drive end-to-end strategic innovation and execution on AbbVie's highest priority commercial assets in partnership with the program-leading Asset Strategy Team and content-focused deliverable teams. Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law: The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position.
Sr. Manager / Associate Director, Publications And Medical Information (Contract) Nurix Therapeutics, Inc.Sr. Manager / Associate Director, Publications And Medical Information (Contract)Brisbane, CAManage the drafting process for clinical publications (with vendor/agency), tracking timelines and ensuring timely reviews, approvals, and submissions. Nurix aims to establish degrader-based treatments at the forefront of patient care, writing medicine's next chapter with a new script to outmatch disease.
Associate Director, Scientific Publications Summit Therapeutics IncAssociate Director, Scientific PublicationsPalo Alto, CA$174,000–$204,000 / yearHARMONi: Phase 3 clinical study which was intended to evaluate ivonescimab combined with chemotherapy compared to placebo plus chemotherapy in patients with EGFR-mutated, locally advanced or metastatic non-squamous NSCLC who were previously treated with a 3rd generation EGFR TKI. Overview of Role: The Associate Director, Scientific Publications provides strategic and operational leadership for global publication activities, ensuring the timely, compliant, and high-quality dissemination of scientific data.
Associate Director, PNT Ecosystem & Strategic Partnerships Iridium Satellite, LLCAssociate Director, PNT Ecosystem & Strategic PartnershipsRedwood City, California$190,000–$248,000 / yearFoster and develop a highly effective team of strategic partnership and business development professionals to execute Iridium's chipset partnership strategy, expand the PNT ecosystem, and achieve long-term business growth objectives. Position Summary, Job Requirements & Responsibilities: What We’re Looking For: Iridium is seeking an Associate Director, PNT Ecosystem & Strategic Partnerships to lead the development and execution of Iridium's chipset and platform partner strategy for its next-generation Positioning, Navigation, and Timing (PNT) services.
Associate Director Clinical PharmacologySenior Clinical Pharmacologist Oncology AbbVie IncAssociate Director Clinical PharmacologySenior Clinical Pharmacologist OncologySouth San Francisco, CASenior Clinical Pharmacologist: PhD with 0 years of experience, or Pharm D with 2+ years of experience in a relevant field, Master's Degree or equivalent education and typically 8+ years of experience, Bachelor's Degree or equivalent education and typically 10+ years of experience; (*relevant field includes experience with PK, PBPK, PK-PD, Pharmacometrics or systems pharmacology, Drug metabolism/Transporters). PhD with typically 4+ years of experience or Pharm D with typically 6+ years of experience in a relevant field, Master's Degree or equivalent education and typically 12+ years of experience, Bachelor's Degree or equivalent education and typically 14+ years of experience;(*relevant field includes experience with PK, PBPK, PK-PD, Pharmacometrics or systems pharmacology, Drug metabolism/Transporters).
Associate Director, Clinical Biomarkers Lead Biogen IncAssociate Director, Clinical Biomarkers LeadSan Francisco, CA$161,000–$222,000 / yearRegular employees are eligible to receive both short term and long-term incentives, including cash bonus and equity incentive opportunities, designed to reward recent achievements and recognize your future potential based on individual, business unit and company performance. We are seeking a highly motivated and experienced Associate Director, Clinical Biomarkers Lead to support clinical biomarker development activities for our portfolio of immunology and neuromuscular clinical programs.
Associate Director, Precision Medicine & Companion Diagnostics Revolution Medicines IncAssociate Director, Precision Medicine & Companion DiagnosticsRedwood City, CA$186,000–$233,000 / yearThe Opportunity: Revolution Medicines is offering a highly visible opportunity for talented and motivated individual to join our Precision Medicine Companion Diagnostics team as an Associate Director, Companion Diagnostics within the Translational Medicine function, which supports CDx development across RevMed portfolio. The company's RAS(ON) inhibitors daraxonrasib (RMC-6236), a RAS(ON) multi-selective inhibitor; elironrasib (RMC-6291), a RAS(ON) G12C-selective inhibitor; zoldonrasib (RMC-9805), a RAS(ON) G12D-selective inhibitor; and RMC-5127, a RAS(ON) G12V-selective inhibitor, are currently in clinical development.
Associate Director, Precision Medicine & Companion Diagnostics Revolution MedicinesAssociate Director, Precision Medicine & Companion DiagnosticsRedwood City, California$186,000–$233,000 / yearRevolution Medicines is offering a highly visible opportunity for talented and motivated individual to join our Precision Medicine Companion Diagnostics team as an Associate Director, Companion Diagnostics within the Translational Medicine function, which supports CDx development across RevMed portfolio. Direct the development, outsourcing and validation of clinically applicable in vitro diagnostic assays through the development lifecycle of molecules, including design, implement and oversee diagnostic testing and registration strategy and timely communication with key internal and external stakeholders.
Associate Director, Global Regulatory Affairs Project Management Revolution MedicinesAssociate Director, Global Regulatory Affairs Project ManagementRedwood City, California$186,000–$233,000 / yearDrive the operational planning, coordination, and tracking of new drug marketing application submission activities across cross-functional Filing Teams (including Regulatory, Medical Writing, Nonclinical, Clinical, Safety, Biostatistics, CMC / Pharmaceutical Development and Manufacturing, etc. and external consultants), supporting the Global Filing Lead’s strategic vision. The ideal candidate will have an in-depth understanding of oncology drug development and demonstrated hands-on regulatory project management experience supporting early- and late-stage registrational programs, including the execution of global new drug marketing applications, in alignment with corporate objectives.
Associate Director, Client Advisory PathstoneAssociate Director, Client AdvisorySan Francisco, California$120,000–$160,000 / yearOur services include investment advisory, as well as integrated planning and coordination across key areas such as tax strategy, risk management guidance, wealth and estate planning support, philanthropic planning, and family governance — helping clients navigate complexity and make informed decisions aligned with their goals. With more than 20 office locations and over $185 billion in client assets under management, advisory, administration, and related services, Pathstone has expanded significantly over the past five years, reflecting sustained momentum and continued investment in our team and platform.
Associate Director, Drug Substance Manufacturing - Upstream Process Vera Therapeutics Inc.Associate Director, Drug Substance Manufacturing - Upstream ProcessBrisbane, CA$175,000–$210,000 / yearWorking with the CMC team and other key functions such as project management, QA and Regulatory, the ideal candidate must be an outstanding leader with a proven track record of overseeing all drug-substance upstream manufacturing activities at the CMO site, including process scale-up, technology transfers, validations, PPQ campaign support, continuous process improvements, and post-approval lifecycle management of commercially approved products. The individual will serve as a subject matter expert (SME) in upstream processes for outsourced drug-substance manufacturing, technology transfer, life cycle management, and global regulatory submissions of complex Biologics, monoclonal antibodies, and other recombinant therapeutics.
Associate Director, Stability Management Exelixis Inc.Associate Director, Stability ManagementAlameda, CA$172,000–$244,000 / yearEDUCATION/EXPERIENCE/KNOWLEDGE & SKILLS: Education/Experience: BS/BA degree in related discipline and a minimum of eleven years of related experience; or, MS/MA degree in related discipline and a minimum of nine years of related experience; or, PhD degree in related discipline and a minimum of five years of related experience; or, Equivalent combination of education and experience. Manage activities related to drug substance and drug product stability testing, both commercial and clinical: Write and review stability protocols according to International Conference on Harmonization (ICH) guidelines.
Associate Director of Development, H&S Stanford UniversityAssociate Director of Development, H&SStanford, CA$145,539–$168,544 / yearThe H&S Development team partners with the Dean''s office, department chairs, center directors, and colleagues across University Development to secure philanthropic support for the school''s most pressing priorities - from named professorships and graduate fellowships to research initiatives and capital projects. Take responsibility for a wide range of fundraising activities, including maintaining an active level of contacts, identifying new prospective donors and volunteers, providing stewardship, and coordinating volunteer fundraising efforts.
Supervising Staff Attorney & Associate Director UC Law SFSupervising Staff Attorney & Associate DirectorSan Francisco, CA$115,000–$120,000 / yearServe one designated day per week as the on-call attorney assigned to file same-day habeas petitions and motions for temporary restraining orders for individuals arrested by ICE in the Bay Area and referred to the BAHN. The Supervising Attorney's primary duty will be to staff weekly on-call shifts for BAHN and file same-day habeas petitions and motions for temporary restraining orders in the Northern District of California for people who qualify.
Associate Director, Chemical Engineering Nurix Therapeutics IncAssociate Director, Chemical EngineeringBrisbane, CA$189,800–$216,700 / yearThe Associate Director, Chemical Engineering will work closely with the CMC team and colleagues in cross-functional departments to provide scientific, technical, and hands-on leadership and oversight of facility and equipment operations at Contract Development Manufacturing Organizations (CDMOs) to support bexobrutideg drug substance manufacturing process optimization and scale-up. Nurix is seeking an experienced, independent, and highly motivated individual who will be accountable for end‑to‑end chemical engineering support of bexobrutideg (NX-5948) drug substance (DS) from late‑stage development through commercial launch, including oversight of external manufacturing sites.
Associate Director, Pharmacovigilance Operations Nurix Therapeutics IncAssociate Director, Pharmacovigilance OperationsBrisbane, CA$229,500–$255,867 / yearThis role serves as the PVO lead for assigned products, driving in-stream quality review, regulatory submission oversight, retrospective quality review, and reconciliation activities, while partnering cross-functionally with Clinical Operations, Data Management, and Regulatory Affairs. Position: The Associate Director, Pharmacovigilance Operations (PVO) is responsible for all PV operational and compliance aspects of assigned Nurix products across the product lifecycle - from First-In-Human (FIH) studies through post-marketing - and for oversight of the end-to-end management of Individual Case Safety Reports (ICSRs).
Associate Director, Program Development Stanford UniversityAssociate Director, Program DevelopmentStanford, CAProgram development is a collaborative and iterative process involving faculty, corporate client partners, and other Stanford units, to create meaningful and impactful learning experiences for senior corporate executives. This could be in the context of creating open enrollment programs for individual leaders, custom programs for clients from organizations around the world, or other educational products.
Associate Director, U.S. VOXZOGO marketing BioMarin Pharmaceutical IncAssociate Director, U.S. VOXZOGO marketingSan Rafael, CA$164,300–$225,940 / yearOur revolutionary treatments for conditions like achondroplasia (the most common form of dwarfism), PKU (phenylketonuria), CLN2, a form of Batten disease, and a number of forms of MPS (mucopolysaccharidosis) offer new possibilities for patients and families who previously had few, if any, available options. The ideal candidate will bring relevant experience in biotech/pharma marketing across multiple disease states, a strong track record of driving value in competitive markets, and a passion for improving patient outcomes in rare disease.
Full-time Associate Director PREMIER ACADEMY WALNUT INCFull-time Associate DirectorWalnut, CAFull timeYou will work closely with the Campus Director and tutoring staff to ensure students receive excellent academic support and that tutors are well-supported in delivering that support. We are Premier Academy Walnut, a tutoring center committed to providing students with an enriching, well-rounded experience to help them achieve their academic goals.