• 4.8

    Senior Pricing Analyst

    Leidos
    Senior Pricing Analyst Job, Remote or Gaithersburg, MD
    Opens new tab
    The Leidos pay range for this job level is a general guideline only and not a guarantee of compensation or salary. The Civil Group at Leidos has an opening for a Senior Pricing Analyst.
    Senior Level
    Bachelors Required
    23d ago
    Opens new tab
  • 4.8

    Database Developer - Remote

    Leidos Holdings Inc.
    Database Developer Job, Remote or Ashburn, VA
    The Homeland Security Solutions Operation within Leidos is seeking a Database Developer with strong systems, software, cloud, and Agile experience to support a complex program to provide Agile development and operations and maintenance for critical systems on a mission-critical program supporting the Passenger Systems Program Directorate (PSPD) within Customs and Border Protection (CBP). The Leidos pay range for this job level is a general guideline only and not a guarantee of compensation or salary. The majority of work can be done remotely, with occasional onsite presence in Ashburn, VA. Leidos is a Fortune 500 technology, engineering, and science solutions and services leader working to solve the world's toughest challenges in the defense, intelligence, civil, and health markets.
    Senior Level
    Bachelors Required
    42d ago
  • 4.7

    Associate Principal, Regulatory Science & Strategy

    Iqvia Holdings Inc.
    Principal Associate Job, Remote or Falls Church, VA
    As an Associate Principal within the IQVIA Regulatory Science and Strategy Practice, you will bring scientific expertise, relationship-building skills, and program management expertise to help IQVIA win and execute on RWE regulatory strategy business. Our projects include advisory consulting on regulatory strategy and rationalizing use of real word evidence for regulatory decision making. These projects can be stand alone or a component of a large project for a life sciences client. The main focus of the Associate Principal role is to deliver outstanding program and study leadership, while building trusted relationships with all external and internal stakeholders. Responsibilities * Develop and deliver insightful, value-added strategies that address complex client issues. Create and elevate new opportunities through the identification of value-added follow-on work and identify new revenue opportunities with existing and new client organizations. * Act as principal owner of program engagements, in some cases with mentoring from senior staff. Ultimate responsibility for client satisfaction and delivering high levels of quality. In many cases, this will require application of scientific / healthcare expertise as well as leadership acumen. * Allocate direction, advice, and intellectual leadership to clients and delivery teams. This includes working with other IQVIA teams to ensure the larger program objectives are achieved across multi-stakeholder collaborations. * Provide high level input and ensure development of key reports and presentations that are essential to program delivery. * Contribute on or lead thought leadership and internal initiatives. * Remain current on latest regulatory trends and clients in order to anticipate and identify new business challenges and issues with assigned opportunities. * Mentor, coach, and share subject matter expertise with others to help develop individuals and capabilities delivering world-class solutions for clients. Qualifications Our ideal candidate will have * US location (work from home), preference for East Coast US with ability to travel to Washington DC. * A Bachelor's degree and an advanced degree related to health care (for example, epidemiology, health economics, health outcomes, health administration, pharmacy, medical doctor). Experience may substitute for advanced degree. * In addition to advanced degree, 3-7 years (depending on advanced degree and hiring level) relevant experience in regulatory programs and studies. * Strong project management, program management, and leadership skills; particularly multi-stakeholder leadership. * Acumen with real-world data, real-world evidence, clinical outcomes assessments, and study design. Should also have broad understanding of the pharmaceutical and medical device industries. * Able to work in environment with ambiguity and help develop the structure as the team grows. * Learning agility and willingness to continuously improve how IQVIA structure and deliver successful regulatory science-related initiatives. * Some flexibility to support client-facing business travel (10-25%). IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible - to help our customers create a healthier world. Learn more at https://jobs.iqvia.com We are committed to providing equal employment opportunities for all, including veterans and candidates with disabilities. https://jobs.iqvia.com/eoe As the COVID-19 virus continues to evolve, IQVIA's ability to operate and provide certain services to customers and partners necessitates IQVIA and its employees meet specific requirements regarding vaccination status. https://jobs.iqvia.com/covid-19-vaccine-status
    Mid Level
    Senior Level
    Management
    Bachelors Required
    55d ago
  • 4.8

    Release Manager - 50% remote

    Leidos Holdings Inc.
    Release Manager Job, Remote or Bethesda, MD
    Our next Release Manager will provide technical and administrative oversight, management, and execution of the entire release management lifecycle for the D3P system in our Bethesda, MD office (with opportunity for partial telework 2-3 days per week). The Leidos Innovations Center(LInC) has an exciting opening for you, our next Release Manager to play a critical role with design, engineering, development and deployment of software for the DOMEX Technology Platform (DTP) DOMEX Data Discovery Platform (D3P) Modernization program.
    Junior Level
    Management
    28d ago
  • 4.7

    Finance Manager (Remote/Hybrid)

    Iqvia
    Finance Manager Job, Remote or Los Angeles, CA
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    Provides financial analysis and insight to segment of a larger business. Provides control, coordination and management of data flow for strategic planning, management reporting, annual budgeting, monthly forecasting, and ad-hoc analysis. Supports month-end accounting close by reviewing actuals, analyzing variances and related project detail, making required journal entries and accruals as required. **This role is hybrid/remote and will require some time in the King of Prussia, PA office. Local candidates preferred.** Essential Functions: P&L Management for Supplier Services Annual Planning and Monthly Forecasting Variance analysis & mitigation strategies Monthly Closing Activities (Accruals, Prepaids, WIP) Barter reporting and fair value analysis Balance sheet reconciliation FTE & Other Opex Controls Supplier Valuation Analysis Preparation of Appropriations Requests for supplier contracts Administration of supplier contracts, understanding of renewals, contract minimums and annual true ups Various ad-hoc projects and requests Respond to quarterly audit inquiries Coordinate contract changes with AP Experience: 5+ years of progressively responsible experience in business analysis, accounting and finance. Qualifications: Strong Excel and financial modeling skills, basic accounting skills (accruals, journal entries) Minimum education requirement: Bachelor's in Accounting or Finance Ability to prioritize and coordinate multiple work requirements to meet deadlines. Ability to build business relationships with finance and non-finance functions Effective verbal and written communication skills Knowledge of Microsoft Office applications Preferred but not Required: Experience with multiple financial systems (Hyperion, SAP, Salesforce) Understanding of legal contracts and ability to provide guidance on financial terms of contracts Experience with complex financial modeling Understanding of healthcare, software, and/or consulting industries Experience working in a multi-national, matrix organization Strong grasp of monthly closing process, budgeting & forecasting requirements of a publicly traded company
    Mid Level
    Management
    Bachelors Required
    20d ago
    Opens new tab
  • 4.7

    Senior or Medical Director, Board Certified/Eligible in Oncology/Hematology, home-based; IQVIA Biotech

    Iqvia
    Medical Director Job, Remote or Rockville, MD
    No matter your role, everyone at IQVIA, including our colleagues at Q Solutions, contributes to our shared goal of improving human health. LI-ALUCAS IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. Join us as a **Senior or Medical Director Board Certified/Eligible in Oncology/ Hematology** and be part of our expanding Medical Services division. The primary role of the Medical Director is to provide medical oversight for clinical trials by serving as Medical Monitor for studies conducted by IQVIA Biotech Clinical on behalf of sponsor companies. We are hiring at IQVIA Biotech.
    Senior Level
    Professional
    Executive
    Doctorate Preferred
    Easy Apply
    60d+ ago
  • 4.7

    Sr. Director, Medical Strategy Lead - Cardiovascular (Home-based)

    Iqvia Holdings Inc.
    Senior Director Job, Remote or Rockville, MD
    The Senior Medical Director also provides review, advice, and leadership for potentially or actually awarded clinical research programs. The Senior Medical Director provides medical and scientific support to clinical research programs, study teams and investigators. * Supervises and manages Medical Director activities The Senior Medical Director role is a team member participant role and functions in a matrix report to project teams much like other members of the project teams. * Assists with drafting of standard operating procedures and working practices regarding all Medical Director activities
    Mid Level
    Senior Level
    Professional
    Executive
    Doctorate Preferred
    New
    6d ago
  • 4.9

    Associate Director, Regulatory CMC Devices & Combination Products

    Biogen Idec
    Associate Director Job, Remote or rote, PA
    Job Description What You'll Do * Accountable for devices / combination products related strategy, planning, definition of content, preparation, review and approval of global regulatory CMC submissions and responses to Health Authority questions. * Identify supporting documents required for global submissions and negotiates the delivery of approved technical source documents in accordance with project timelines. * Accountable review and approval of CMC submissions and responses to Health Authority questions in line with agreed global regulatory strategy, and within agreed timelines. * Highlight and proactively communicates anticipated and ongoing critical Regulatory CMC issues throughout the product lifecycle, in a timely manner, to key stakeholders as appropriate. * Leads cross-functional teams responsible for the preparation of submissions and responses to Health Authority CMC questions for assigned projects/products. * Ensures effective communication of CMC regulatory strategy, risks, and overall plans to leadership and teams. * Partner with regulatory regional leads for exchange of project/product related information and submission planning. * Accountable/responsible for the roles and functions of the CMC RRL for the geographical region in which the CMC GRL role is located. * Represent Global RegCMC-devices/combo product on due diligence and divestment teams as assigned by the Global RegCMC LT. * Lead or provide input to Global RegCMC initiatives and cross functional work streams as assigned by Global RegCMC LT. Qualifications Who You Are This candidate must have proven leadership and abilities to work cross-functionally and across cultures, has strong communication, regulatory CMC knowledge and interpersonal skills. Qualifications Required Skills * BS degree in Life Sciences, Engineering, Biotechnology, or relevant Pharmaceutical Science is preferred plus a minimum of 10 years relevant experience in the pharmaceutical industry or a regulatory authority CMC review capacity * 5+ years of experience in Regulatory CMC and preferably 2 years professional experience in combination product development and/or lifecycle management * Successful leadership in delivering device / combination product related CMC sections of marketing authorizations, clinical trial applications (CTA/IND) and post-approval submissions for new biological, oligonucleotide, and/or chemical entities * Broad background of registration experience gained from working in the pharmaceutical industry or a regulatory authority in one or more of the ICH regions. * Extensive experience of direct communication and negotiation with regulatory agencies on combination product specific topics * Knowledge of global guidance, regulations and ICH/GMP requirements * Demonstrated competence in leading cross-functional teams and operating within a matrix organizational structure Additional Information This role is responsible for defining regulatory device / combination product CMC strategy, planning and the preparation of global CMC regulatory submissions to achieve timely approvals with a focus on development and/or commercial programs. Responsibilities include; actively leading the development and implementation of CMC regulatory strategy for specific devices and combination products, identifying and assessing global regulatory risks, implementing filing readiness strategy, leading global CMC Health Authority interactions, and providing regulatory CMC leadership on the cross functional sub teams for the assigned program. Why Biogen? Our mission to find therapies for neurological and rare diseases is a unique focus within our industry and this shared purpose is what connects us as a team. We work together to overcome obstacles and to follow the science. We are resilient as we strive to make an impact on our patients' lives and on changing the course of medicine. Together, we pioneer. Together, we thrive. The base compensation range for this role is $130,900 to $218,100. Base salary is determined by a combination of factors including, but not limited to, job related years of relevant experience, internal equity, and location of the job. Additionally, this role is eligible for participation in Biogen's LTI grants and other incentive programs. Biogen offers a full range of benefits that include medical, dental, life, long and short-term disability insurances, vacation, end-of-year shutdown, and 401K participation and matching contributions.
    Senior Level
    Executive
    Bachelors Required
    New
    2d ago
  • 4.9

    Associate Director, Regulatory CMC Devices & Combination Products

    Biogen Idec
    Associate Director Job, Remote or rote, PA
    Job Description What You'll Do * Accountable for devices / combination products related strategy, planning, definition of content, preparation, review and approval of global regulatory CMC submissions and responses to Health Authority questions. * Identify supporting documents required for global submissions and negotiates the delivery of approved technical source documents in accordance with project timelines. * Accountable review and approval of CMC submissions and responses to Health Authority questions in line with agreed global regulatory strategy, and within agreed timelines. * Highlight and proactively communicates anticipated and ongoing critical Regulatory CMC issues throughout the product lifecycle, in a timely manner, to key stakeholders as appropriate. * Leads cross-functional teams responsible for the preparation of submissions and responses to Health Authority CMC questions for assigned projects/products. * Ensures effective communication of CMC regulatory strategy, risks, and overall plans to leadership and teams. * Partner with regulatory regional leads for exchange of project/product related information and submission planning. * Accountable/responsible for the roles and functions of the CMC RRL for the geographical region in which the CMC GRL role is located. * Represent Global RegCMC-devices/combo product on due diligence and divestment teams as assigned by the Global RegCMC LT. * Lead or provide input to Global RegCMC initiatives and cross functional work streams as assigned by Global RegCMC LT. Qualifications Who You Are This candidate must have proven leadership and abilities to work cross-functionally and across cultures, has strong communication, regulatory CMC knowledge and interpersonal skills. Qualifications Required Skills * BS degree in Life Sciences, Engineering, Biotechnology, or relevant Pharmaceutical Science is preferred plus a minimum of 10 years relevant experience in the pharmaceutical industry or a regulatory authority CMC review capacity * 5+ years of experience in Regulatory CMC and preferably 2 years professional experience in combination product development and/or lifecycle management * Successful leadership in delivering device / combination product related CMC sections of marketing authorizations, clinical trial applications (CTA/IND) and post-approval submissions for new biological, oligonucleotide, and/or chemical entities * Broad background of registration experience gained from working in the pharmaceutical industry or a regulatory authority in one or more of the ICH regions. * Extensive experience of direct communication and negotiation with regulatory agencies on combination product specific topics * Knowledge of global guidance, regulations and ICH/GMP requirements * Demonstrated competence in leading cross-functional teams and operating within a matrix organizational structure Additional Information This role is responsible for defining regulatory device / combination product CMC strategy, planning and the preparation of global CMC regulatory submissions to achieve timely approvals with a focus on development and/or commercial programs. Responsibilities include; actively leading the development and implementation of CMC regulatory strategy for specific devices and combination products, identifying and assessing global regulatory risks, implementing filing readiness strategy, leading global CMC Health Authority interactions, and providing regulatory CMC leadership on the cross functional sub teams for the assigned program. Why Biogen? Our mission to find therapies for neurological and rare diseases is a unique focus within our industry and this shared purpose is what connects us as a team. We work together to overcome obstacles and to follow the science. We are resilient as we strive to make an impact on our patients' lives and on changing the course of medicine. Together, we pioneer. Together, we thrive. The base compensation range for this role is $130,900 to $218,100. Base salary is determined by a combination of factors including, but not limited to, job related years of relevant experience, internal equity, and location of the job. Additionally, this role is eligible for participation in Biogen's LTI grants and other incentive programs. Biogen offers a full range of benefits that include medical, dental, life, long and short-term disability insurances, vacation, end-of-year shutdown, and 401K participation and matching contributions.
    Senior Level
    Executive
    Bachelors Required
    New
    2d ago
  • 4.9

    Associate Director, Global Regulatory Lead CMC

    Biogen Idec
    Associate Director Job, Remote or rote, PA
    Job Description About This Role This role is responsible for defining CMC regulatory strategy, planning and preparation of global CMC regulatory submissions to achieve timely approvals with a focus on commercial programs. Responsibilities include actively leading the development and implementation of CMC regulatory strategy for specific small molecule, oligonucleotide, biologics projects or devices, identifying and assessing global regulatory risks, implementing filing readiness strategy, leading global CMC Health Authority interactions, and providing regulatory CMC leadership on cross functional sub teams for the assigned program. What You'll Do * Accountable for strategy, planning, definition of content, preparation, review and approval of global CMC regulatory submissions and responses to Health Authority questions. * Ensure that the global regulatory CMC strategy for assigned products are consistent with the teams and business goals, missions and objectives and meet Health Authority requirements. * Identify supporting documents required for global submissions and negotiates the delivery of approved technical source documents in accordance with project timelines. * Accountable review and approval of CMC submissions and responses to Health Authority questions in line with agreed global regulatory strategy, and within agreed timelines. * Lead cross-functional teams responsible for the preparation of submissions and responses to Health Authority CMC questions for assigned projects/products. * Highlight and proactively communicates anticipated and ongoing critical CMC regulatory issues throughout the product lifecycle, in a timely manner, to key stakeholders as appropriate. * Accountable/responsible for the roles and functions of the CMC RRL for the geographical region in which the CMC GRL role is located. * Participate in skill development and coaching of other Global RegCMC Team members as required. * Accountable for the coordination and overall global approval of regulatory assessments for CMC changes. Qualifications Who You Are You are an enthusiast team-worker, passionate about motivating people to be the best they can be, working inclusively, collaboratively, effectively and efficiently with others internally and externally. You are able to create strong, productive working relationships in a global setting with many different cultures. Required Skills * BS degree in Life Sciences, Engineering, Biotechnology, or relevant Pharmaceutical Science; Graduate degree preferred. * At least 7+ years relevant experience in the pharmaceutical industry or a regulatory authority CMC review capacity, with at least 5+ years of experience in Regulatory CMC (Commercial) and preferably 2 years professional experience in pharmaceutical manufacturing for small molecules, analytical development, and quality assurance/control or related technical field. * Successful leadership in delivering CMC sections of marketing authorizations, clinical trial applications (CTA/IND) and post-approval submissions for new biological, oligonucleotide, and/or chemical entities * Broad background of registration experience gained from working in the pharmaceutical industry or a regulatory authority in one or more of the ICH regions. * Extensive experience of direct communication and negotiation with regulatory agencies on CMC topics * Knowledge of global guidance, regulations and ICH/GMP requirements * Demonstrated competence in leading cross-functional teams and operating within a matrix organizational structure * Ability to work, with accountability, both independently and within project teams or committees to attain group goals and key project milestones. * Demonstrated inclusive leadership and emotional intelligence, along with verbal and written remote working communication abilities. * Demonstrated ability to pioneer and execute on an agreed global regulatory CMC strategy and ensure that results are in alignment with business priorities. Additional Information The CMC RRL is primary contact for affiliates on regulatory CMC activities in the assigned region (i.e. United States, Canada, Latin and South America where located in the United States) Why Biogen? Our mission to find therapies for neurological and rare diseases is a unique focus within our industry and this shared purpose is what connects us as a team. We work together to overcome obstacles and to follow the science. We are resilient as we strive to make an impact on our patients' lives and on changing the course of medicine. Together, we pioneer. Together, we thrive. The base compensation range for this role is $130,900 to $218,100. Base salary is determined by a combination of factors including, but not limited to, job related years of relevant experience, internal equity, and location of the job. Additionally, this role is eligible for participation in Biogen's LTI grants and other incentive programs. Biogen offers a full range of benefits that include medical, dental, life, long and short-term disability insurances, vacation, end-of-year shutdown, and 401K participation and matching contributions.
    Mid Level
    Senior Level
    Executive
    Bachelors Preferred
    New
    2d ago
  • 4.9

    Manager, Clinical Site Contracts Management

    Biogen Idec
    Clinical Data Management Manager Job, Remote or rote, PA
    You use excellent judgement to balance achieving results with protecting Biogen's interests. * Monitor trends and contribute to the development and maintenance of processes, guidelines tools, and templates Support other Biogen functions in direct site contacts to resolve challenges and remove roadblocks Additionally, this role is eligible for participation in Biogen's LTI grants and other incentive programs. This is a cross-functional role and will provide site contract language support and guidance in response to escalations from CROs, liaise with Biogen R&D Legal and other operational roles to resolve complex negotiations, and act as a regional SME to provide input on country level contracts strategy. Biogen offers a full range of benefits that include medical, dental, life, long and short-term disability insurances, vacation, end-of-year shutdown, and 401K participation and matching contributions.
    Mid Level
    Management
    Offers Benefits
    Bachelors Preferred
    8d ago
  • 4.9

    Co-op, Computational Fluid Dynamics of the Central Nervous System

    Biogen Idec
    Computer Systems Operator Job, Remote or Massachusetts
    As an intern or co-op at Biogen, you can expect to be placed on a real project, under the guidance of experienced professionals and subject matter experts who are invested in your career and academic growth. To participate in the Biogen Internship Program, students must meet the following eligibility criteria: Biogen discovers, develops, and delivers worldwide innovative therapies for people living with serious neurological and neurodegenerative diseases. At Biogen, our mission is clear - we are pioneers in neuroscience. We at Biogen are committed to building on our culture of inclusion and belonging that reflects the communities where we operate and the patients who we serve.
    Junior Level
    Masters Required
    15d ago
  • 4.9

    Co-op, Computational Fluid Dynamics of the Central Nervous System

    Biogen Idec
    Computer Systems Operator Job, Remote or Massachusetts
    As an intern or co-op at Biogen, you can expect to be placed on a real project, under the guidance of experienced professionals and subject matter experts who are invested in your career and academic growth. To participate in the Biogen Internship Program, students must meet the following eligibility criteria: Biogen discovers, develops, and delivers worldwide innovative therapies for people living with serious neurological and neurodegenerative diseases. At Biogen, our mission is clear - we are pioneers in neuroscience. We at Biogen are committed to building on our culture of inclusion and belonging that reflects the communities where we operate and the patients who we serve.
    Junior Level
    Masters Required
    15d ago
  • 4.9

    Intern, Computational Biologist

    Biogen Idec
    Computer Science Internship Job, Remote or Massachusetts
    As an intern or co-op at Biogen, you can expect to be placed on a real project, under the guidance of experienced professionals and subject matter experts who are invested in your career and academic growth. Toward this end, single-nucleus RNA-seq data have been invaluable resource, and Biogen has been pioneering in generation and analysis of such data from postmortem human patient samples and mouse and iPSC-derived model systems. You will join an experienced team of data scientists and have opportunities to closely collaborate with the broader Biogen R&D community. Biogen discovers, develops, and delivers worldwide innovative therapies for people living with serious neurological and neurodegenerative diseases. At Biogen, our mission is clear - we are pioneers in neuroscience. Education PhD candidate in either computational biology, bioinformatics, systems biology, computer science or in related fields We at Biogen are committed to building on our culture of inclusion and belonging that reflects the communities where we operate and the patients who we serve.
    Internship
    Entry Level
    16d ago
  • 4.9

    Intern, Computational Biologist

    Biogen Idec
    Computer Science Internship Job, Remote or Massachusetts
    As an intern or co-op at Biogen, you can expect to be placed on a real project, under the guidance of experienced professionals and subject matter experts who are invested in your career and academic growth. Toward this end, single-nucleus RNA-seq data have been invaluable resource, and Biogen has been pioneering in generation and analysis of such data from postmortem human patient samples and mouse and iPSC-derived model systems. You will join an experienced team of data scientists and have opportunities to closely collaborate with the broader Biogen R&D community. Biogen discovers, develops, and delivers worldwide innovative therapies for people living with serious neurological and neurodegenerative diseases. At Biogen, our mission is clear - we are pioneers in neuroscience. Education PhD candidate in either computational biology, bioinformatics, systems biology, computer science or in related fields We at Biogen are committed to building on our culture of inclusion and belonging that reflects the communities where we operate and the patients who we serve.
    Internship
    Entry Level
    16d ago
  • 4.9

    Sr. Manager, Global Regulatory Sciences Quality

    Biogen Idec
    Senior Quality Manager Job, Remote or rote, PA
    Additionally, this role is eligible for participation in Biogen's LTI grants and other incentive programs. Biogen offers a full range of benefits that include medical, dental, life, long and short-term disability insurances, vacation, end-of-year shutdown, and 401K participation and matching contributions. * Facilitate timely GVP/GCP audit responses and evaluate proposed corrective actions, and/or preventative actions, including effectiveness checks for compliance with applicable regulations, guidelines, and Biogen procedures.
    Mid Level
    Senior Level
    Management
    Offers Benefits
    Bachelors Preferred
    14d ago
  • 4.9

    Associate Director, Global Regulatory Lead CMC

    Biogen Idec
    Associate Director Job, Remote or rote, PA
    Mid Level
    Senior Level
    Executive
    Bachelors Preferred
    New
    2d ago
  • 4.9

    Sr. Manager, Identity and Access Management (SailPoint) Program Delivery Lead - Remote

    Biogen Idec
    Senior Manager, Program Management Job, Remote or rote, PA
    As the Senior Identity and Access Management (IAM) Business and Technical Analyst, you will utilize your knowledge of IAM to enhance Biogen's current state capabilities. At Biogen, our mission is clear: we are pioneers in neuroscience. Biogen also manufactures and commercializes biosimilars of advanced biologics. Biogen discovers, develops, and delivers worldwide innovative therapies for people living with serious neurological and neurodegenerative diseases.
    Senior Level
    Management
    Masters Required
    22d ago
  • 4.9

    Sr. Manager, Identity and Access Management (SailPoint) Program Delivery Lead - Remote

    Biogen Idec
    Senior Manager, Program Management Job, Remote or rote, PA
    As the Senior Identity and Access Management (IAM) Business and Technical Analyst, you will utilize your knowledge of IAM to enhance Biogen's current state capabilities. At Biogen, our mission is clear: we are pioneers in neuroscience. Biogen also manufactures and commercializes biosimilars of advanced biologics. Biogen discovers, develops, and delivers worldwide innovative therapies for people living with serious neurological and neurodegenerative diseases.
    Senior Level
    Management
    Masters Required
    22d ago
  • 4.9

    Sr. Analyst, Data Analytics

    Biogen Idec
    Senior Data Analyst- Job, Remote or rote, PA
    * Drive Value across Biogen Procurement by providing insights to Procurement leaders and category managers specific to category strategies This Sr. Analyst, Data Analytics role is responsible for using a variety of tools to provide data analysis, extracts, reports and dashboards in support of the Global Procurement organization as a member of Global Procurement Analytics (GPA) team.
    Mid Level
    Senior Level
    Bachelors Preferred
    37d ago

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Biogen may also be known as or be related to Biogen, Biogen Idec, Biogen Idec Inc. (2003–2015), Biogen Inc, Biogen Inc. and Biogen, Inc.