Associate Director, Clinical Safety Scientist - Daiichi Sankyo
Bernards, NJ 07920
About the Job
Join a Legacy of Innovation 110 Years and Counting!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 world-class science and technology
With more than 100 years of scientific expertise and a presence in more than 20 countries, Daiichi Sankyo and its 15,000 employees around the world draw upon a rich legacy of innovation and a robust pipeline of promising new medicines to help people
Under the Group’s 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.SummaryThis position serves as the Clinical Safety Scientist Lead for a large, late-stage program or multiple early-stage programs, in order to proactively perform safety surveillance and risk management in partnership with Product Safety Lead(s), Clinical Safety Physician(s), and cross-functional team in support of benefit risk profile throughout product life cycle
Collaborates with the PSL(s) to proactively plan and prioritize safety surveillance and risk management activities for assigned product(s), including resource planning, oversees team's workload, anticipates potential issues and works towards resolving issues, and escalates and communicates issues, as appropriate
Oversees or leads the coordination of Safety Management Team (SMT)/Product-level safety meetings, maintains roster, calendar, and minutes, and communicate materials, in support of the PSL
Independently evaluates safety data of any source to identify potential safety signals and performs safety analysis/evaluation
May contribute to safety action recommendations, and communication and risk minimization plans
Presents assessment to the appropriate forums, including SMT or other cross-functional teams
Oversees or tracks safety signals in the global electronic signal tracking tool
Collaborates with the PSL(s) to plan and prioritize activities for Biologics License Applications (BLAs)/Marketing Authorization Applications (MAAs), and local country submissions
Collaborates with PSL/Clinical Safety Physician(s) and cross-functional team to develop safety strategy, key safety messages, and review and author safety sections of Common Technical Document (CTD)
May oversee multiple simultaneous submissions to ensure harmonized approach of safety sections of the submission dossier, where applicable, and to ensure timelines and business objectives are met
Subject matter expert (SME) in 2 or more focus areas
May supervise a team of Clinical Safety Scientists for assigned product(s),or serve as a preceptor for post-doctoral fellows
Provides guidance, and mentors and coaches junior Clinical Safety Scientists.ResponsibilitiesRisk Management (Signal identification, evaluation, mitigation):This position serves as the Clinical Safety Scientist Lead for a large, late-stage program or multiple early-stage programs, in order to proactively perform safety surveillance and risk management in partnership with Product Safety Lead(s), Clinical Safety Physician(s), and cross-functional team in support of benefit risk profile throughout product life cycle.Develops materials (presentation, safety analyses / evaluation, etc.) for SMT/Product-level safety meetings, including recommended safety actions, and communication and risk minimization plans.Authors or oversees the development of minimum core product safety requirements for inclusion in Clinical study protocols (CSPs) and Informed Consent Forms (ICFs), for assigned product(s)Authors or oversees the development of the Safety Management Plan for assigned product(s)Independently evaluates safety data of any source to identify potential safety signals and performs safety analysis/evaluation
May contribute to safety action recommendations, and communication and risk minimization plans
Presents assessment to the appropriate forums, including SMT or other cross-functional teams.Oversees or tracks safety signals in the global electronic signal tracking tool.Safety Communication:Collaborates with PSL(s) or Clinical Safety Physician(s) for assigned product(s) or clinical studies to review and revise CSPs, ICFs, Clinical Study Reports (CSRs), and build and review Statistical Analysis Plans (SAPs) and statistical outputs (tables, figures, and listings [TFLs]), and other clinical study documentsAuthors or oversees the development of safety sections of Investigator's Brochure, aggregate reports (DSUR/PLL), Prescribing information, Company Core Data Sheet (CCDS), Risk Management Plan(s) (RMPs)Collaborates with PSL(s) and cross-functional team for assigned product(s) to author or contribute to regulatory authority requests or communicationEnsures consistent and unified safety message throughout multiple documentsCTD submissions/Others:Collaborates with the PSL(s) to plan and prioritize activities for Biologics License Applications (BLAs)/Marketing Authorisation Applications (MAAs), and local country submissions
Collaborates with PSL/Clinical Safety Physician(s) and cross-functional team to develop safety strategy, key safety messages, and review and author safety sections of Common Technical Document (CTD)
May oversee multiple simultaneous submissions to ensure harmonized approach of safety sections of the submission dossier, where applicable, and to ensure timelines and business objectives are metSubject matter expert (SME) in 2 or more focus areasSupports Data Monitoring Committees (DMCs) and due diligence activities for assigned product(s), as neededActs as audit/inspection Subject Matter Expert (SME) for safety surveillance and risk management for assigned product(s), through inspection readiness preparation, and may serve as the primary or back-up SME, and may collaborate with team on CAPAs, including CAPA responses and approvalsProject Management:Collaborates with the PSL(s) to proactively plan and prioritize safety surveillance and risk management activities for assigned product(s), including resource planning, oversees team’s workload, anticipates potential issues and works towards resolving issues, and escalates and communicates issues, as appropriateOversees or leads the coordination of Safety Management Team (SMT)/Product-level safety meetings, maintains roster, calendar, and minutes, and communicate materials, in support of the PSLMay oversee multiple simultaneous complex projects, ie, multiple submissions, to ensure harmonized approach of safety sections, where applicable, and to ensure timelines and business objectives are metPeople Management/Leadership:May supervise a team of Clinical Safety Scientists for assigned product(s), or serve as a preceptor for post-doctoral fellowsProvides guidance, and mentors and coaches junior Clinical Safety ScientistsQualifications: Successful candidates will be able to meet the qualifications below with or without a reasonable accommodation.Education Qualifications (from an accredited college or university)PharmD preferred.PhD preferred.Bachelor's degree in healthcare required.Experience Qualifications:3-5 years of proven experience with an advanced degree required.6-9 years of experience with a bachelor’s degree required.Clinical development or post-marketing experience to be able to apprehend safety context through the product life cycle.Understanding of Safety Risk Management internal and external environment, including applicable regulations and guidance'sAbility to engage team and cross-functional team members to facilitate continuous flow of information to meet business objectives.Manages conflict and negotiates constructively.Ability to develop and build healthy working relationships to enable higher performance.Effective oral and written communication skillsDemonstrated ability to handle more than one complex project simultaneously, prioritizing and recognizing key issues.Demonstrates effectiveness in working in a multidisciplinary and matrixed environment.Understanding of tools, standards, and approaches used to efficiently evaluate safety is desirable.Microsoft Word, Excel, PowerPoint skills, and Project management skillsAble to work independently with minimal direct supervision.Physical RequirementsGlobal Travel 20% of TimeDaiichi Sankyo, Inc
is an equal opportunity/affirmative 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
SummaryLocation: Basking Ridge, NJType: Full time
With more than 100 years of scientific expertise and a presence in more than 20 countries, Daiichi Sankyo and its 15,000 employees around the world draw upon a rich legacy of innovation and a robust pipeline of promising new medicines to help people
Under the Group’s 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.SummaryThis position serves as the Clinical Safety Scientist Lead for a large, late-stage program or multiple early-stage programs, in order to proactively perform safety surveillance and risk management in partnership with Product Safety Lead(s), Clinical Safety Physician(s), and cross-functional team in support of benefit risk profile throughout product life cycle
Collaborates with the PSL(s) to proactively plan and prioritize safety surveillance and risk management activities for assigned product(s), including resource planning, oversees team's workload, anticipates potential issues and works towards resolving issues, and escalates and communicates issues, as appropriate
Oversees or leads the coordination of Safety Management Team (SMT)/Product-level safety meetings, maintains roster, calendar, and minutes, and communicate materials, in support of the PSL
Independently evaluates safety data of any source to identify potential safety signals and performs safety analysis/evaluation
May contribute to safety action recommendations, and communication and risk minimization plans
Presents assessment to the appropriate forums, including SMT or other cross-functional teams
Oversees or tracks safety signals in the global electronic signal tracking tool
Collaborates with the PSL(s) to plan and prioritize activities for Biologics License Applications (BLAs)/Marketing Authorization Applications (MAAs), and local country submissions
Collaborates with PSL/Clinical Safety Physician(s) and cross-functional team to develop safety strategy, key safety messages, and review and author safety sections of Common Technical Document (CTD)
May oversee multiple simultaneous submissions to ensure harmonized approach of safety sections of the submission dossier, where applicable, and to ensure timelines and business objectives are met
Subject matter expert (SME) in 2 or more focus areas
May supervise a team of Clinical Safety Scientists for assigned product(s),or serve as a preceptor for post-doctoral fellows
Provides guidance, and mentors and coaches junior Clinical Safety Scientists.ResponsibilitiesRisk Management (Signal identification, evaluation, mitigation):This position serves as the Clinical Safety Scientist Lead for a large, late-stage program or multiple early-stage programs, in order to proactively perform safety surveillance and risk management in partnership with Product Safety Lead(s), Clinical Safety Physician(s), and cross-functional team in support of benefit risk profile throughout product life cycle.Develops materials (presentation, safety analyses / evaluation, etc.) for SMT/Product-level safety meetings, including recommended safety actions, and communication and risk minimization plans.Authors or oversees the development of minimum core product safety requirements for inclusion in Clinical study protocols (CSPs) and Informed Consent Forms (ICFs), for assigned product(s)Authors or oversees the development of the Safety Management Plan for assigned product(s)Independently evaluates safety data of any source to identify potential safety signals and performs safety analysis/evaluation
May contribute to safety action recommendations, and communication and risk minimization plans
Presents assessment to the appropriate forums, including SMT or other cross-functional teams.Oversees or tracks safety signals in the global electronic signal tracking tool.Safety Communication:Collaborates with PSL(s) or Clinical Safety Physician(s) for assigned product(s) or clinical studies to review and revise CSPs, ICFs, Clinical Study Reports (CSRs), and build and review Statistical Analysis Plans (SAPs) and statistical outputs (tables, figures, and listings [TFLs]), and other clinical study documentsAuthors or oversees the development of safety sections of Investigator's Brochure, aggregate reports (DSUR/PLL), Prescribing information, Company Core Data Sheet (CCDS), Risk Management Plan(s) (RMPs)Collaborates with PSL(s) and cross-functional team for assigned product(s) to author or contribute to regulatory authority requests or communicationEnsures consistent and unified safety message throughout multiple documentsCTD submissions/Others:Collaborates with the PSL(s) to plan and prioritize activities for Biologics License Applications (BLAs)/Marketing Authorisation Applications (MAAs), and local country submissions
Collaborates with PSL/Clinical Safety Physician(s) and cross-functional team to develop safety strategy, key safety messages, and review and author safety sections of Common Technical Document (CTD)
May oversee multiple simultaneous submissions to ensure harmonized approach of safety sections of the submission dossier, where applicable, and to ensure timelines and business objectives are metSubject matter expert (SME) in 2 or more focus areasSupports Data Monitoring Committees (DMCs) and due diligence activities for assigned product(s), as neededActs as audit/inspection Subject Matter Expert (SME) for safety surveillance and risk management for assigned product(s), through inspection readiness preparation, and may serve as the primary or back-up SME, and may collaborate with team on CAPAs, including CAPA responses and approvalsProject Management:Collaborates with the PSL(s) to proactively plan and prioritize safety surveillance and risk management activities for assigned product(s), including resource planning, oversees team’s workload, anticipates potential issues and works towards resolving issues, and escalates and communicates issues, as appropriateOversees or leads the coordination of Safety Management Team (SMT)/Product-level safety meetings, maintains roster, calendar, and minutes, and communicate materials, in support of the PSLMay oversee multiple simultaneous complex projects, ie, multiple submissions, to ensure harmonized approach of safety sections, where applicable, and to ensure timelines and business objectives are metPeople Management/Leadership:May supervise a team of Clinical Safety Scientists for assigned product(s), or serve as a preceptor for post-doctoral fellowsProvides guidance, and mentors and coaches junior Clinical Safety ScientistsQualifications: Successful candidates will be able to meet the qualifications below with or without a reasonable accommodation.Education Qualifications (from an accredited college or university)PharmD preferred.PhD preferred.Bachelor's degree in healthcare required.Experience Qualifications:3-5 years of proven experience with an advanced degree required.6-9 years of experience with a bachelor’s degree required.Clinical development or post-marketing experience to be able to apprehend safety context through the product life cycle.Understanding of Safety Risk Management internal and external environment, including applicable regulations and guidance'sAbility to engage team and cross-functional team members to facilitate continuous flow of information to meet business objectives.Manages conflict and negotiates constructively.Ability to develop and build healthy working relationships to enable higher performance.Effective oral and written communication skillsDemonstrated ability to handle more than one complex project simultaneously, prioritizing and recognizing key issues.Demonstrates effectiveness in working in a multidisciplinary and matrixed environment.Understanding of tools, standards, and approaches used to efficiently evaluate safety is desirable.Microsoft Word, Excel, PowerPoint skills, and Project management skillsAble to work independently with minimal direct supervision.Physical RequirementsGlobal Travel 20% of TimeDaiichi Sankyo, Inc
is an equal opportunity/affirmative 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
SummaryLocation: Basking Ridge, NJType: Full time
Source : Daiichi Sankyo