Jobs at Daiichi Sankyo
2,115 open positions
Associate Director, Resource Management
Company: Daiichi Sankyo
Location: Other US Location
Posted Mar 21, 2024
Daiichi Sankyo Group, a global pharmaceutical company with over 100 years of experience, is seeking a candidate for a position in Analytical Resource Management. The role involves partnering with the Head of Resource Management to establish expert capacity planning, strategic and scenario planning, and use of analytical tools. The candidate will be responsible for driving the development and implementation of project and non-project FTE algorithms, Planisware (TRIDENT) Time-Card tracking, resource analyses reports, and functional business partnering. The position requires strong project management skills, cross-functional drug development coordination/resource management experience, and industry experience in pharmaceuticals or life sciences. The candidate should have a Bachelor's Degree, preferably an advanced degree, and 7 or more years of relevant experience. The role involves up to 10% domestic and international travel.
Associate Director, Pharmacoepidemiology
Company: Daiichi Sankyo
Location: Other US Location
Posted Mar 16, 2024
<p><b>Join a Legacy of Innovation 110 Years and Counting<b> <p> <p>Daiichi Sankyo Group is dedicated to the creation and supply of innovative pharmaceutical therapies to improve standards of care and address diversified unmet medical needs of people globally by leveraging our worldclass science and technology With more than 100 years of scientific expertise and a presence in more than 20 countries Daiichi Sankyo and its 16000 employees around the world draw upon a rich legacy of innovation and a robust pipeline of promising new medicines to help people Under the Groups 2025 Vision to become a Global Pharma Innovator with Competitive Advantage in Oncology Daiichi Sankyo is primarily focused on providing novel therapies in oncology as well as other research areas centered around rare diseases and immune disorders <p> <p><b>SUMMARY<b> <p> <ul><li>The Associate Director Pharmacoepidemiology position provides epidemiologic methodological and analytic support to Daiichi Sankyo products This position contributes to or independently leads the design preparation and analysis of epidemiologic studies including realword evidence RWE supporting senior management in various epidemiological activities<li> <li>This position independently carries out various functions eg literature reviews study design preparation of data for statistical analysis to obtain background rates for development of safety documents eg RMP support SMTs SERM or other safetyrelated meetings and study protocols<li> <li>This position independently manages relationships with internal CSPV Regulatory Clinical Medical Affairs HEOR and other stakeholders to ensure expectations are clearly defined and met across participating teams and external stakeholders<li> <li>Must be able to prioritize and manage multiple projects and vendors Provides strong vendorinternal communication to ensure successful and timely deliverables This position solves complex technical problems with experience and expertise Finally this position makes tactical decisions utilizing input from upper management that impacts more than one project team at a time This position will also support planning for epidemiology strategy for assigned products<li> <ul><p><b>RESPONSIBILITIES<b> <p> <ul><li>Identify study needs draft protocols and contribute to epidemiology strategy for assigned products Collaborate with epidemiology colleagues and Product Safety Lead to identify research gaps develop protocols conduct analyses and interpretcommunicate scientific findings to internal andor external stakeholders<li> <li>Conduct literature searches and reviews targeted andor systematic and prepare summariesreports<li> <li>Work on crossfunctional teams to formulate responses to health authority queries<li> <li>Provide epidemiologic support to internal stakeholders and disseminate study findings through presentations andor publications in peerreviewed scientific journals<li> <li>Assess clinical trial andor other data sources to contextualize safety events for assigned product Research natural history of disease to characterize background event rates<li> <li>Design and conduct postauthorization safety studies and contribute to the development and review of safety documents including Risk Management Plans<li> <li>Efficiency of Process SOP Leads the process and provides guidance Proactively ensures regulatory and good pharmacoepidemiology practices<li> <ul><p><b>QUALIFICATIONS<b> Successful candidates will be able to meet the qualifications below with or without a reasonable accommodation <p> <p><b>Education Qualifications<b> from an accredited college or university <p> <ul><li>PhD ScD or DrPH degree in Epidemiology or a PharmD PhD or MD with a masters degree in Epidemiology required<li> <ul><p><b>Experience Qualifications<b> <p> <p>2+ years post terminal degree of professional experience in Epidemiology function within the pharmaceutical industry <p> <ul><li>2+ years of industry experience or postdoctoral degree experience in a relevant industry academia or public sector<li> <li>2+ years of expertise using database management eg MSAccess and statistical programming eg SAS required<li> <li>Must have demonstrated ability to formally plan execute and deliver projects<li> <li>Must have Project Management experience <li> <ul><p><b>Licenses and Certifications<b> <p> <ul><li>If degree is outside of epidemiology then a certificate in epidemiologypharmacoepidemiology is required<li> <ul><p>Daiichi Sankyo Inc is an equal opportunityaffirmative action employer 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<p>
Associate Director, Data Management
Company: Daiichi Sankyo
Location: Other US Location
Posted Mar 19, 2024
Daiichi Sankyo Group, a global pharmaceutical company with over 100 years of experience, is dedicated to creating innovative therapies for diverse medical needs. The company focuses on oncology, rare diseases, and immune disorders. The position in question manages end-to-end data management services for projects, collaborating with CROs and vendors. The role requires strong knowledge of Electronic Data Capture, clinical operations, and regulatory requirements. The ideal candidate should have a Master's or Bachelor's degree in life sciences, 7+ years of data management experience, and experience managing people and initiatives.
Senior Study Associate
Company: Daiichi Sankyo
Location: Other US Location
Posted Apr 14, 2024
Daiichi Sankyo Group, a global pharmaceutical company with over 100 years of experience, is dedicated to creating innovative therapies for diverse medical needs. The company is primarily focused on oncology, rare diseases, and immune disorders. The role of Study Associate Manager within Clinical Operations involves planning and executing clinical studies, providing clinical trial management support, tracking CRO and vendor performance, and ensuring compliance with Daiichi Sankyo's Clinical Study Oversight Plan. Key responsibilities include reconciling TMF document trackers, distributing study documents, providing administrative support, and participating in training and career development. Successful candidates should have a Bachelor's Degree in Life Sciences, relevant clinical development experience, and CRA experience is preferred.
Manager, Global Aggregate Reporting
Company: Daiichi Sankyo
Location: Other US Location
Posted Mar 18, 2024
The position will support Daiichi-Sankyo global aggregate reporting for investigational and post-marketed medicinal products within the Clinical Safety and Pharmacovigilance department. The role will provide managerial leadership and oversight of AR activities and workflow, and will be responsible for managing the scheduling and workflow of aggregate reports.
Manager, Biostatistics
Company: Daiichi Sankyo
Location: Other US Location
Posted Apr 12, 2024
The text describes the Daiichi Sankyo Group's dedication to innovation and improving healthcare standards. It also outlines the responsibilities and qualifications for a statistical support position within the company.
Associate Director, Tech Management Lead mAb
Company: Daiichi Sankyo
Location: Other US Location
Posted Mar 16, 2024
Daiichi Sankyo Group, a global pharmaceutical company with over 100 years of experience, is dedicated to creating innovative therapies for diverse medical needs. The company is primarily focused on oncology, rare diseases, and immune disorders. The Technology Management Lead is responsible for managing technology transfer of manufacturing processes for investigational and commercial drugs, leading the Site Launch Team, and ensuring smooth transitions. The role involves creating and implementing manufacturing plans, conducting scouting activities for CDMOs, and supporting regulatory submissions. Qualifications include a Bachelor's or Master's degree in a relevant field and at least 7 years of industry experience, or a PhD with at least 5 years of experience.
Senior Associate, US Marketing
Company: Daiichi Sankyo
Location: Other US Location
Posted Mar 18, 2024
Daiichi Sankyo Group, a global pharmaceutical company with over 100 years of experience, is dedicated to creating innovative therapies for diverse medical needs. The company focuses on oncology, rare diseases, and immune disorders, in addition to its strong portfolio in cardiovascular diseases. The Senior Associate, US Marketing role involves supporting commercialization efforts, managing brand websites, and working on promotional campaigns. The ideal candidate should have a Bachelor's degree in health sciences, pharmaceutical experience, and a proven track record in strategic initiatives.
Associate Director, biostatistics
Company: Daiichi Sankyo
Location: Other US Location
Posted Mar 16, 2024
<p>Join a Legacy of Innovation 110 Years and Counting <p> <p>Company is committed to diversity and inclusion We are an equal opportunity employer including veterans and people with disabilities <p> <p>SummaryPosition leads complex studies in study design statistical analysis and interpretation of results with some supervision This position contributes to specific aspects of drug development plans with minimal supervision and contributes to documents submitted to Health Authorities globally with some supervision This position also guides contract research organization CRO programmers and statisticians in preparing analysis files and performing statistical analyses Additionally this position interacts with study teams as well as statisticians and programmers at CROs This position works under some supervision to solve complex study problems <p> <p>Responsibilities <p> <p> 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 Acts as main statistical contact for the assigned studies and projects Provides guidance to study team on all aspects of statistical activities collaborates closely with data manager to ensure high quality data <p> <p> 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 prespecified product profile <p> <p> CRO Vendor Oversight Review CROvendor proposal and budget Establishes procedures through regular interaction setting expectation on deliverables and timelines to guide CRO biostatistician and statistical programmers on complex studies Ensures deliverables are accurate and delivered according to the timelines <p> <p> Global Health Authority Interaction Negotiation Contributes to documents submitted to Health Authorities globally by providing input for the interaction or by writing the interaction document May participate in meeting or teleconferences with Health Authorities <p> <p> Global 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 <p> <p>Qualifications Successful candidates will be able to meet the qualifications below with or without a reasonable accommodation <p> <p>Education Qualifications from an accredited college or university <p> <p> Masters Degree in statistics or biostatistics required <p> <p> PhD in statistics or biostatistics preferred Experience Qualifications <p> <p> 8+ Years of relevant experience in the pharmaceutical industry with a masters degree required <p> <p> 5+ Years of relevant experience in the pharmaceutical industry with a PhD preferred TravelAbility to travel up to 10 <p> <p>Daiichi Sankyo Inc is an equal opportunityaffirmative action employer 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<p>
Director, Biostatistics (Indication Lead)
Company: Daiichi Sankyo
Location: Other US Location
Posted Apr 20, 2024
Daiichi Sankyo Group, a global pharmaceutical company with over 100 years of experience, is dedicated to creating innovative therapies for diverse medical needs. The company is primarily focused on oncology, rare diseases, and immune disorders. The role involves leading complex studies, providing input to drug development plans, interacting with global project teams and health authorities, and overseeing CROs. The ideal candidate should have a Master's or PhD in statistics or biostatistics, 7+ years of pharmaceutical industry experience, and be able to travel up to 20%, including international travel.
Director, Sustainability
Company: Daiichi Sankyo
Location: Other US Location
Posted Mar 18, 2024
Daiichi Sankyo Group, a global pharmaceutical company with over 100 years of experience, is seeking a candidate for a Sustainability program position in the US. The role involves setting strategy, implementing sustainability initiatives, and collaborating with global teams. The candidate must have a Bachelor's Degree, preferably a Master's, and at least 10 years of ESG or Sustainability Management experience. Travel to Japan and Germany is required annually.
Director, Global eQMS Management GMP QA
Company: Daiichi Sankyo
Location: Other US Location
Posted Apr 07, 2024
Daiichi Sankyo Group, a global pharmaceutical company with over 100 years of experience, is dedicated to creating innovative therapies for unmet medical needs. The Director, Global eQMS Management QA GMP, is responsible for managing and enhancing the company's electronic Quality Management System (eQMS) with a focus on GMP/GDP activities. This role involves collaborating with various departments, ensuring global process harmonization, and fostering a quality culture. The ideal candidate should have a Bachelor's or Master's degree in a relevant field, extensive experience in quality management within the pharmaceutical industry, and proven experience in managing electronic Quality Management Systems.