Jobs at Daiichi Sankyo
2,115 open positions
Associate Director, Diagnostic Sciences
Company: Daiichi Sankyo
Location: Other US Location
Posted Sep 15, 2023
Qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected veteran status, age, or any other characteristic protected by law. - Strong organizational and networking skills. - Strong communication and presentation skills. - Strong interpersonal skills and knowledge of intercultural differences. Must be able to travel domestically and internationally Daiichi Sankyo, Inc. is an equal opportunity/affirmative action employer. - Experience in oncology drug development is preferred - Must have at least 3 years' experience in fit-for-purpose clinical biomarker assay development, validation, and implementation in support of multi-site clinical trials. - Ability to adjust priorities in a fast-paced environment. - Collaborate with Translational Scientists, Companion Diagnostic Scientists and Clinical Scientists and Operations Leads in the review of clinical protocols, laboratory instructions, investigator training, clinical sample analysis, archiving of biomarker test results, and regulatory submission activities for Daiichi Sankyo clinical development. - Global implementation experience is highly desirable - Experience and expertise in spatial platforms (e.g. Travel Ability to travel up to 20%.
Director, HEOR
Company: Daiichi Sankyo
Location: Other US Location
Posted Aug 23, 2023
Daiichi Sankyo Group, a global pharmaceutical company with over 100 years of experience, is seeking a HEOR expert to develop strategies for assigned products. The role involves providing HEOR strategic direction, contributing to product development plans, and leading the development of value propositions. The candidate must have a Master's or PhD in a relevant discipline, 10+ years of experience in healthcare or pharmaceutical industry, and hands-on experience with HEOR methodologies. The role requires collaboration with internal and external stakeholders, and travel up to 30%.
Associate Director, Strategic Value & Access Marketing - In-line Products
Company: Daiichi Sankyo
Location: Other US Location
Posted Aug 26, 2023
Qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected veteran status, age, or any other characteristic protected by law. Education Qualifications (from an accredited college or university) - Bachelor's Degree required - MBA or advanced degree preferred Experience Qualifications - 7 or More Years overall related experience, preferably within pharmaceuticals, or commensurate education/experience required - 1 or More Years Pharmaceutical sales preferred - 1 or More Years sales training or brand marketing preferred - 1 or More Years pricing and access experience preferred - 2 or More years pharmaceutical managed care sales/account management, preferred - managed markets marketing experience, marketing research, preferred Daiichi Sankyo, Inc. is an equal opportunity/affirmative action employer. - Understand, monitor, and evaluate the effect of US healthcare marketplace changes and evolving delivery systems. Seek and provide routine assessments of potential impact of policy changes, health care trends and customer changes, and recommended courses of action to maintain access to assigned brands. This includes supporting all Market Access customers, including payers, community practices, hospital systems, pathways and GPOs. Develop strategic market access recommendations for in-line and pipeline products in all assigned channels. Responsibilities - Leads the development and implementation of market access marketing and strategy for all Market Access field teams (and Sales Representatives, HEOR teams when appropriate) with assigned customer segments. - Contributes to the National Leadership Meeting and National Oncology Meeting process for Market Access field teams across the portfolio for assigned customer segments or brands - Responsibility includes the creation of all PMRT approved tools and appropriate training resources in order to support optimal execution - Establishment of account call continuum objectives for the period with market access peers and Account Manager Directors - Work collaboratively with Market Access Training to ensure appropriate training for external customer interaction Qualifications: Successful candidates will be able to meet the qualifications below with or without a reasonable accommodation. This includes: - Development of the branded value proposition and any ancillary materials, including training resources to support brand strategy at field meetings (NLM, NOM, launch meetings) - Partner with Market Access Insights and Analytics to develop and implement market research plan for assigned products - Identify GPO opportunities to support brand strategy and communicate with GPO team and brand marketing team to align strategy - Responsible for ensuring close collaboration with Brand teams and co-promote partners (if applicable) to generate success as defined by KPIs in targeted Market Access accounts and monitored via marketing feedback systems by taking a leadership role within Brand Teams and co-promote partners. They work cross-functionally to support annual brand planning, leading the Market Access budget, and understanding any potential access barriers for their product.
Associate Director, Global Project Management
Company: Daiichi Sankyo
Location: Other US Location
Posted Sep 16, 2023
Qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected veteran status, age, or any other characteristic protected by law. Ensure Project Team awareness of the Global Development Process (GDP). Education Qualifications (from an accredited college or university) Bachelor's Degree requiredadvanced degree (i.e., MS, MBA or PhD) in a scientific discipline with additional relevant experience preferredProject Management Professional (PMP) Certification and/or training in project management preferred Experience Qualifications 7 or More Years experience in pharmaceutical industry preferred4 or More Years drug development project management experience or equivalentIndustry experience: Direct, global pharmaceutical or drug development experience required Daiichi Sankyo, Inc. is an equal opportunity/affirmative action employer. Works with finance and team members to secure adequate resourcing and budget and tracks team performance against the budget.Maintains global integrated project plans, project timelines, risk management, plans and communication plans. Independently identifies issues and leads issue resolution meetings. Leads risk identification, prioritization and mitigation planning processes.Identifies and recommends PM best practices for the broader GPM&L organization. Identifies problems and works with team to resolve. This position will report to the Sr. Director, Group Leader, GPM&L. Leverages their network to influence across the organization.Manages project status in the project management information systems and communicates risks/issues to GPM senior management in a timely manner. Supports scenario planning and critical path analyses.
Associate Director, Data Management
Company: Daiichi Sankyo
Location: Other US Location
Posted Sep 15, 2023
Qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected veteran status, age, or any other characteristic protected by law. Finally, this position has strong skills in continuous improvement, project management, change management, and risk management. Operational Efficiency / Continuous Improvement:Provides leadership within Data Management by partnering with internal and external stakeholders to optimize Data Management technology, processes, and standards (improving quality/inspection readiness, decreasing cycle times, and reducing costs).Leads multidisciplinary process improvement initiatives.Leverages comprehensive Data Management expertise to promote best practices across the Clinical Trial lifecycle. Functional Expertise:Reviews/approves clinical study related documents that are owned by other functions (e.g., Protocols, Statistical Analysis Plans, Clinical Study Reports).Actively participates in audits and inspections. Responsibilities Leadership, Direction, and Strategy:Provides data management (DM) expertise and guidance to the project team regarding the data management DM activities and deliverablesEstablishes Data Management strategy at the project and/or study level for a larger number of projects/studies with greater complexity.Ensures data management deliverables for all studies within the project/program level meets quality , time and cost effectiveLeads functional and/or multidisciplinary teams working on projects/studies and/or initiatives.Lead and manage the standardized Data Management Process and Procedures for consistency across programs and organizationProactively identifies and manages risks at the project and/or study level for a larger number of projects/studies with greater complexity.May manage Data Management full-time and/or contract staff.Project Management:Plans and directs the conduct of Data Management activities for assigned projects/studies through outsourcing (e.g., study startup, study conduct, study closeout, and reporting).Provides oversight for Data Management CRO and other third party vendors to ensure compliance with the protocol, external/internal standards, Good Clinical Practices (GCPs), applicable regulatory guidelines, Policies, SOPs, and other relevant guidelines.Ensures Data Management deliverables meet/exceed project/study team expectations regarding quality, time, and cost and that Data Management documentation is filed/archived according to applicable Daiichi Sankyo and regulatory requirements. Education Qualifications (from an accredited college or university) Master's Degree in life sciences or related field preferredBachelor's Degree in life sciences or related field preferred Experience Qualifications 7 or more years data management and/or related work experience in a medical device or pharmaceutical company, or similar environment (e.g., CRO) preferred4 or more years combined experience managing people and/or initiatives preferred Daiichi Sankyo, Inc. is an equal opportunity/affirmative action employer. This position has solid verbal/written skills, analytical, organizational, and interpersonal skills and works effectively with people at different levels and from different disciplines and cultures. Additionally, this position possesses advanced knowledge of clinical operations and processes and relevant regulatory requirements. This position provides leadership within Data Management by partnering with internal and external stakeholders to optimize Data Management technology, processes, and standards. Additionally, this position develops/proposes strategies within Data Management and collaborates cross-functionally to ensure successful outcomes for projects/studies.
Associate Director, Pharmacoepidemiology
Company: Daiichi Sankyo
Location: Other US Location
Posted Aug 25, 2023
Daiichi Sankyo Group, a global pharmaceutical company with over 100 years of experience, is seeking an Associate Director of Pharmacoepidemiology. The role involves providing epidemiologic support, designing and analyzing studies, managing relationships with internal and external stakeholders, and ensuring adherence to regulatory practices. The ideal candidate will have a PhD in Epidemiology or a PharmD, PhD, or MD with a Master's in Epidemiology, along with 1-2 years of professional experience in the pharmaceutical industry. Proficiency in database management and statistical programming is required.
Director, Advanced Pharmacometrics
Company: Daiichi Sankyo
Location: Other US Location
Posted Sep 11, 2023
Daiichi Sankyo Group, a global pharmaceutical company with over 100 years of experience, is seeking a model-based analysis expert to inform the clinical development of their assets. The role involves analyzing complex multi-source data, collaborating across functions, and applying regulatory guidelines. The ideal candidate should have a PharmD with a clinical pharmacology research fellowship or a PhD in pharmacology or pharmaceutical sciences, along with 4+ years of industry experience and 1+ year of drug development experience.
Senior Scientist / Associate Director, RACMC
Company: Daiichi Sankyo
Location: Other US Location
Posted Sep 06, 2023
Daiichi Sankyo Group, a global pharmaceutical company with over 100 years of experience, is seeking a Regulatory Affairs CMC Project Representative. The role involves managing multiple biological developmental projects, preparing submission documents, and interacting with health authorities. The ideal candidate should have a Bachelor's Degree in Life Science, an MS/PhD in a scientific discipline preferred, and 4+ years of direct or related CMC regulatory experience. The position requires advanced knowledge of regulations, strong technical knowledge, and excellent oral and writing skills.
Senior Director, Global Project Management and Leadership
Company: Daiichi Sankyo
Location: Other US Location
Posted Sep 16, 2023
Qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected veteran status, age, or any other characteristic protected by law. Ensure organizational awareness of the Global Development Processes. Can step in, as needed, on behalf of the Global Team Leader to deliver presentations to Sr Management. Education Qualifications (from an accredited college or university) Bachelor's Degree Bachelor's degree in a scientific discipline with additional relevant experience is requiredAdvanced degree (i.e., MS, MBA or PhD) in a scientific discipline with additional relevant experience preferred Experience Qualifications 10 or More Years in a drug development PM role or related role In Biotech or Pharmaceutical industry10 or More Years Demonstrated success as a project manager/leader in planning and executing strategies for global drug development: early stage, late stage and life cycle management10 or More Years Proven track record as a leader/influencer in a global role10 or More Years Direct people management experience with ability to identify and recruit talent preferred Licenses and Certifications Certified Project Management Professional (PMP)-PMI and/or training in project management preferred Travel Ability to travel up to 5% Daiichi Sankyo, Inc. is an equal opportunity/affirmative action employer. Responsibilities Project Responsibilities Independently manage or lead strategy development for high complexity drug development projects/programs. Departmental Responsibilities Work independently within a matrix environment and coach, influence and mentor more junior PMs, Team members and project stakeholders.As a TA lead or Lead on a Business Collaboration, will contribute to portfolio management by participating in global TA strategy committees and have an in depth understanding of project strategies/plans.As a staff manager, responsible for coaching PMs on project-related issues including review of their Monthly Project Summary Reports and governance presentations. Manages the Global Project Team(s) in partnership with the Global Team Leader to drive strategy development and create an integrated product development plan and timelines. Responsible for talent development and ensuring that staff have actionable development plans and receive ongoing coaching and feedback.Provide leadership to the Global PM function by supporting budget and resource management, annual goals setting as well as strategic direction for the department.Identify and implement PM best practices for the broader GPM organization. Qualifications: Successful candidates will be able to meet the qualifications below with or without a reasonable accommodation. Ensure execution of overall plan and annual goals.Responsible for developing and maintaining a high performing team.Generate critical path analyses and lead scenario planning with GPT to select best option understanding cost and timeline implications.Resolve complex problems and identify gaps in the project or organization.Mobilize others to gain alignment with the most Sr leaders and secure resources for the project.Accountable for the accuracy of project status in the project management information systems, for preparing scope change proposals and stage gate proposals for formal presentation to senior management.
Executive Director, Study Management Group Head
Company: Daiichi Sankyo
Location: Other US Location
Posted Sep 12, 2023
Daiichi Sankyo Group, a global pharmaceutical company with over 100 years of experience, is dedicated to creating innovative therapies for unmet medical needs. The company is primarily focused on oncology, rare diseases, and immune disorders. The Executive Director, Global Clinical Operations Study Management Group Head, is responsible for strategic oversight of study management and delivery across all therapeutic areas. This role involves partnering with various stakeholders, ensuring robust planning, driving standardization, and fostering a performance-driven culture. The ideal candidate should have a Bachelor's Degree, 15+ years of industry experience, and proven expertise in global drug development, performance management, and change management.
Manager, Omnichannel Marketing
Company: Daiichi Sankyo
Location: Other US Location
Posted Aug 20, 2023
Daiichi Sankyo Group is dedicated to creating innovative pharmaceutical therapies to improve standards of care and address unmet medical needs. The company is focused on providing novel therapies in oncology and other research areas.
Associate Director Biostatistics
Company: Daiichi Sankyo
Location: Other US Location
Posted Sep 15, 2023
Qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected veteran status, age, or any other characteristic protected by law. Responsibilities Protocol Development, Case Report Form (CRF; review), Statistical Analysis Plan (SAP), Statistical Analysis, Results Interpretation, and clinical study report (CSR): Leads statistical activities for complex studies including study design, protocol development, CRF review, SAP development, analysis files development, statistical analysis accuracy validation, results interpretation and CSR input and review. Establishes procedures through regular interaction, setting expectation on deliverables and timelines to guide CRO biostatistician and statistical programmers on complex studies. Additionally, this position interacts with study teams, as well as statisticians and programmers at CROs. May participate in meeting or teleconferences with Health AuthoritiesGlobal BDO Strategy to Improve Drug Development: Primarily participates and may occasionally lead moderately complex initiatives, with some level of supervision, to improve the harmonization and efficiency of drug development which leads to cost savings and shortened timelines for the company. Education Qualifications (from an accredited college or university) PhD in statistics or biostatistics preferred Experience Qualifications 5 or More Years of relevant experience in the pharmaceutical industry required Daiichi Sankyo, Inc. is an equal opportunity/affirmative action employer. Qualifications: Successful candidates will be able to meet the qualifications below with or without a reasonable accommodation. Acts as main statistical contact for the assigned studies and projects. This position works under some supervision to solve complex study problems. Provides guidance to study team on all aspects of statistical activities; collaborates closely with data manager to ensure high quality data.Drug Development Strategy: Provides input to multiple aspects of the development plan to ensure the study designs at each phase of the development are scientifically sound, can fulfill regulatory requirements and deliver the pre-specified product profile.CRO / Vendor Oversight: Review CRO/vendor proposal and budget.