Associate Director, Statistics 3316 Takeda Development Center AmericasAssociate Director, StatisticsBoston, Massachusetts$154,400–$242,550 / yearCentral to Takeda’s R&D operating model are the pillars of Data & Quantitative Sciences, which are leveraged to support the imperative of becoming a data-driven and scientifically and quantitatively disciplined rigorous organization. The actual base salary offered may depend on a variety of factors, including the qualifications of the individual applicant for the position, years of relevant experience, specific and unique skills, level of education attained, certifications or other professional licenses held, and the location in which the applicant lives and/or from which they will be performing the job.
Associate Director, Machine Learning (Core Algorithms) WhoopAssociate Director, Machine Learning (Core Algorithms)Boston, MassachusettsWe are seeking an Associate Director, Core Algorithms (Cloud) to lead the teams responsible for WHOOP's cloud-based algorithmic intelligence — the models and systems that transform physiological data into the sleep, recovery, and training insights our members rely on daily. This role is also responsible for ensuring our cloud algorithms evolve alongside WHOOP hardware, partnering with Sensor Intelligence and Hardware teams to translate new sensor capabilities into production-grade algorithmic experiences.
Associate Director, Global Labeling Lead 3316 Takeda Development Center AmericasAssociate Director, Global Labeling LeadMassachusettsThe Global Regulatory Labeling Strategy Lead (Associate Director), Plasma-Derived Therapies Business Unit (PDT BU) is a key role in Global Labeling and works under the direction of the Head of Global Labeling and is: Responsible, with minimal supervision for providing regulatory expertise, strategic insight, and guidance to internal stakeholders, including Clinical, Pharmacovigilance, Legal, Scientific, Commercial, to ensure successful development and maintenance of labeling managed within PDT BU’s Global Labeling function, pertaining to pharmaceutical drug and device. In close collaboration with the Takeda R&D labeling function, oversees the direction, management and implementation of the labeling processes, templates, tools and systems to improve efficiency, productivity and quality and consistency across products and compliance with regulatory labeling guidance.
Associate Director - Value, Access, Insights, and Solutions 3310 Takeda Pharmaceuticals U.Associate Director - Value, Access, Insights, and SolutionsLexington, MassachusettsDevelops and maintains a broad network of mutually supportive relationships with internal Takeda colleagues (Medical Product Teams, Medical Communications, VEG, Marketing, Managed Markets, Market Access Channel Strategy, Government External Affairs, Account Management and other affiliates) to ensure US Medical scientific and outcomes research and external affairs strategies are integrated across groups. The Associate Director of Value Access Insights & Solutions is an integral member of the Marketing Content Enablement & Customer Engagement group and is responsible for: Serving as a partner to Product Medical Units, Medical Communications, Medical leads, Field Medical Leaders, Brand Teams, Market Access and Channel Strategy, Public Affairs and other Global and US internal stakeholders to ensure strategic alignment on cross-functional imperatives and initiatives.
Associate Director, Global Regulatory Project Management and Strategic Planning - Oncology 3316 Takeda Development Center AmericasAssociate Director, Global Regulatory Project Management and Strategic Planning - OncologyMassachusettsPartnering with the program Global Regulatory Lead (GRL), co-lead and facilitate product-specific Global Regulatory Team (GRT) meetings and cross-functional submission working groups (SWG) meetings, to oversee, plan and deliver GRT goals and regulatory submissions in accordance with regulatory strategy for complex programs. Operational support may include, but not limited to drafting and preparation of forms and cover letters, providing logistical support for health authority meetings, coordinating briefing book roundtables, drafting regulatory notifications, coordinating and managing regulatory document workflows, inputting information into regulatory information management systems, preparing, checking and tracking regulatory data and lists etc.).
Associate Director of HCP Branded Strategy and Marketing 3310 Takeda Pharmaceuticals U.Associate Director of HCP Branded Strategy and MarketingMassachusettsYou will partner cross-functionally across HCP, Consumer, Field Teams, and other cross-functional teams to bring to life a seamless, insight-based marketing ecosystem that motivates HCPs and drives brand success. The actual base salary offered may depend on a variety of factors, including the qualifications of the individual applicant for the position, years of relevant experience, specific and unique skills, level of education attained, certifications or other professional licenses held, and the location in which the applicant lives and/or from which they will be performing the job.
Associate Director, Medical Content 3310 Takeda Pharmaceuticals U.Associate Director, Medical ContentBoston, MassachusettsMaintain in-depth knowledge of medical communications trends and materials (e.g., scientific platforms, core slide decks, scientific communication plans, digital communication plans) and independently drive updates/revisions to these materials. The actual base salary offered may depend on a variety of factors, including the qualifications of the individual applicant for the position, years of relevant experience, specific and unique skills, level of education attained, certifications or other professional licenses held, and the location in which the applicant lives and/or from which they will be performing the job.
Associate Director, Process Development (Fermentation) ModernaTXAssociate Director, Process Development (Fermentation)Norwood, MassachusettsWe are proud to have been recognized as a Science Magazine Top Biopharma Employer, a Fast Company Best Workplace for Innovators, and a Great Place to Work in the U.S. If you want to make a difference and join a team that is changing the future of medicine, we invite you to visit modernatx.com/careers to learn more about our current opportunities. Moderna is seeking an Associate Director, Process Development to lead upstream/fermentation process development for E. coli-based production of recombinant enzymes, plasmids, and related biological starting materials critical to Moderna’s technology platforms and pipeline programs.
Associate Director / Director, Toxicology Beam TherapeuticsAssociate Director / Director, ToxicologyCambridge, MA$185,000–$260,000 / yearBeam’s suite of gene editing technologies is anchored by base editing, a proprietary technology that is designed to enable precise, predictable and efficient single base changes, at targeted genomic sequences, without making double-stranded breaks in the DNA. Provide toxicology support for regulatory submissions and interactions with health authorities, including the authoring of nonclinical safety sections of US and international regulatory applications, and help resolve nonclinical safety queries.
Associate Director, HEOR) & RWE Connexion Systems + EngineeringAssociate Director, HEOR) & RWEBoston, MAWe are seeking an experienced Associate Director, Health Economics & Outcomes Research (HEOR) & Real-World Evidence (RWE) to lead evidence generation initiatives that demonstrate the clinical, economic, and real-world value of innovative therapies. This is an excellent opportunity for an experienced HEOR professional who enjoys collaborating across Medical Affairs, Market Access, Commercial, and Research teams to influence evidence strategy and support patient access.
Associate Director, Medical Affairs Connexion Systems + EngineeringAssociate Director, Medical AffairsBoston, MAWe are seeking an experienced Associate Director, Medical Affairs to support strategic and operational medical affairs activities within the cholestatic disease space, including biliary atresia. The ideal candidate brings a strong background in Medical Affairs along with the ability to collaborate cross-functionally in a fast-paced, highly scientific environment.
Associate Director, Toxicology (Nonclinical Safety Evaluation) City TherapeuticsAssociate Director, Toxicology (Nonclinical Safety Evaluation)Cambridge, Massachusetts$174,000–$196,000 / yearThe Ideal Candidate • PhD or DVM, or equivalent advanced degree in Toxicology, Pharmacology, Pathology, Veterinary Sciences, or a related field, with 5+ years, Masters with 7+ or a Bachelors with 10+ of relevant experience in biotech or pharmaceutical drug development, or direct experience as a Study Director at a GLP-qualified CRO.• Strong experience overseeing outsourced nonclinical safety studies and critically reviewing protocols, data, and final reports.• The Role We’re seeking an Associate Director, Nonclinical Safety Evaluation (NSE) who will play a pivotal role in overseeing and critically evaluating nonclinical safety studies across City’s RNAi therapeutic programs.
Associate Director, Media Strategy & Execution Amylyx PharmaceuticalsAssociate Director, Media Strategy & ExecutionCambridge, MARemote$173,000–$195,000 / yearDevelop connected media and channel strategies across paid, owned, earned, CRM, web, search, social, programmatic, video/CTV, endemic, non-endemic, and emerging digital channels, ensuring integration with creative, messaging, audience segmentation, and digital experience design. The role requires a strategic operator who can translate insights into actionable media plans, manage investment tradeoffs, strengthen measurement discipline, and continuously optimize the channel ecosystem to improve relevance, efficiency, and business impact.
Associate Director, Quality Operations Amylyx PharmaceuticalsAssociate Director, Quality OperationsCambridge, MARemote$172,000–$194,000 / yearProvide QA review and approval on quality technical agreements, master production records, product specifications (in-process, release, and stability), analytical method qualification/validation documents, method transfer documents, and stability plans. Lead or participate in regular meetings internally and externally as CMC Quality SME to ensure Amylyx’s quality expectations are met in the areas of Good Manufacturing Practice, Good Distribution Practice, and Good Documentation Practice.
Associate Director, Launch and Pre-Launch Forecasting Lead, Global Oncology 3310 Takeda Pharmaceuticals U.Associate Director, Launch and Pre-Launch Forecasting Lead, Global OncologyBoston, MassachusettsThis role sits within the larger Global Insights and Analytics organization in the Oncology Business Unit (OBU) and is responsible for working with stakeholders (including Global/US Marketing, Market Access, etc) to deliver short-range, mid-range and long-range forecasts and relevant strategic insights to drive the business. The actual base salary offered may depend on a variety of factors, including the qualifications of the individual applicant for the position, years of relevant experience, specific and unique skills, level of education attained, certifications or other professional licenses held, and the location in which the applicant lives and/or from which they will be performing the job.
Lead, Global Pricing, Oncology (Associate Director) 3312 Takeda Pharmaceuticals AmericaLead, Global Pricing, Oncology (Associate Director)Boston, Massachusetts$154,400–$242,550 / yearAs a leader in the Global Oncology Pricing Center of Excellence, this high-visibility, high impact position is expected to apply industry-leading strategic and operational capabilities to drive optimal decision-making and inform key pricing decisions. The actual base salary offered may depend on a variety of factors, including the qualifications of the individual applicant for the position, years of relevant experience, specific and unique skills, level of education attained, certifications or other professional licenses held, and the location in which the applicant lives and/or from which they will be performing the job.
Associate Director, Global Regulatory Affairs - GI & Inflammation 3316 Takeda Development Center AmericasAssociate Director, Global Regulatory Affairs - GI & InflammationBoston, Massachusetts$154,400–$242,550 / yearDemonstrates strong skills with increasing independence in the area of regulatory strategy such as understanding broad concepts within regulatory affairs and implications across the organization and globally; proactively identifies regulatory issues; offers creative solutions and strategies, including risk mitigation strategies. Acceptable and independent skills in the area of regulatory strategy such as understanding broad concepts within regulatory affairs and implications across the organization and globally; proactively identifies regulatory issues; offers creative solutions and strategies, including risk mitigation strategies.
Associate Director, Quantitative Clinical Pharmacology (QCP) Lead 3316 Takeda Development Center AmericasAssociate Director, Quantitative Clinical Pharmacology (QCP) LeadBoston, MassachusettsAdvanced knowledge of pharmaceutical industry, overall drug development process with expertise in the cross-functional interfaces with key partners such as Pharmacometrics, Statistics, Drug Safety, Clinical Sciences, Outcomes, Digital Health, Pharmaceutical Sciences/Device, and Global Regulatory Affairs. These scientists (from quantitative clinical pharmacology, statistics, programming, outcomes research and epidemiology, patient safety & pharmacovigilance, digital strategy, library sciences and data architecture/governance) bring their expertise to our global program teams and reimagine our disciplines.
NewAssociate Director, Analytical Development Kymera TherapeuticsAssociate Director, Analytical DevelopmentWatertown, MA$160,000–$240,000 / yearHaving advanced the first degrader into the clinic for immunological diseases, Kymera is focused on building an industry-leading pipeline of oral small molecule degraders to provide a new generation of convenient, highly effective therapies for patients with these conditions. PhD in Analytical Chemistry or related life sciences field is preferred, but not required, with 10+ years of experience in CMC analytical development of small molecule drug substance and oral solid dosage forms.
Associate Director, Global and US Pipeline Forecasting Lead 3310 Takeda Pharmaceuticals U.Associate Director, Global and US Pipeline Forecasting LeadBoston, Massachusetts$154,400–$242,550 / yearThis role sits within the larger Global Insights and Analytics organization in the Oncology Business Unit (OBU) and is responsible for working with stakeholders (including Global/US Marketing, Market Access) to deliver short-, mid-range and long-range forecasts and relevant strategic insights to drive the business. The actual base salary offered may depend on a variety of factors, including the qualifications of the individual applicant for the position, years of relevant experience, specific and unique skills, level of education attained, certifications or other professional licenses held, and the location in which the applicant lives and/or from which they will be performing the job.