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Medical Director Jobs At Alexion Pharmaceuticals

- 101 Jobs

  • Senior Director, US gMG HCP Marketing, Neurology

    The Senior Director, US gMG HCP Marketing, Neurology BU is responsible for driving the development and implementation of the US commercial HCP marketing strategy for Generalized Myasthenia Gravis (gMG). At Alexion, people living with rare and devastating diseases are our Guiding Star. Reporting to the Head of US Marketing, the Senior Director, Neurology will be a high-profile and high impact role within the Neurology Business Unit at Alexion.
    $132k-171k yearly est.4d ago

  • Medical Science Liaison, Great Lakes

    The individual manages and maintains collegial and professional relationships with KOLs and identifies and facilitates collaboration opportunities with Alexion. + Identifying and executing collaboration opportunities between expert KOLs in hematology/nephrology and Alexion medical affairs and clinical development such as publications, investigator-initiated trials, regional advisory boards, training, and speaker development programs The Medical Science Liaison (MSL) is field-based scientific expert that strategically supports the medical and scientific objectives of Alexion's product/s across the product/s life cycle. + Communicating experts' opinion, feedback on new data and clinical trends to Alexion Medical Affairs, TA Area franchises and translate this information into strategic recommendations to enhance science and advance patient care At Alexion, people living with rare and devastating diseases are our Guiding Star. Train Alexion staff on key scientific and medical topics in TA Area + Serving as an Alexion-internal expert in TA Area demonstrating up-to-date and high-level therapeutic expertise. + Developing and maintaining peer-to-peer collaborations with key medical experts in TA Area within the assigned region and become recognized as a consultant on Alexion therapeutic area/s + Communicating and educating Alexion internal customers on local initiatives on disease and treatment guidelines in a timely manner
    $122k-183k yearly est.5d ago

  • Associate Director, Risk Based Study Management (remote

    The Associate Director delegates tasks appropriately, tracks progress, and provides expert technical and process support to team members. The Risk-Based Study Management Associate Director is responsible for directing and coordinating the activities of Risk-Based Study Management (RBSM) staff assigned to projects within Clinical Data Management. In addition, the Associate Director fluently and routinely briefs management on accomplishments, status, and issues under their own initiatives.
    $148k-222k yearly9d ago

  • IT Project Manager

    The IT Project Manager will also partner closely with the R&D IT Portfolio lead to become a leader & trusted advisor for the R&D IT team on IT standards, policies, and guidelines as it relates to RDU IT's Strategic Portfolio Management & Operating Model approach. At Alexion, people living with rare and devastating diseases are our Guiding Star. As part of the R&D IT team of AstraZeneca's Alexion Rare Disease Unit (RDU), the IT Project Manager will be responsible for the planning and execution of IT projects. The IT Project Manager will work closely with the business teams and various IT functions (e.g., infrastructure, solution delivery managers, architects etc.) to deliver on various business transformation initiatives.
    $108k-158k yearly est.14d ago

  • Sr. Manager, Cold Chain Logistics Process (Remote Eligible

    The Senior Manager of Cold Chain Logistics Process is responsible for leading the development and implementation of processes and procedures to ensure the success of cold chain logistics operations within Vertex Pharmaceuticals This position requires close collaboration with logistics service providers, order management teams, quality assurance, and other stakeholders to ensure adherence to regulatory guidelines and meet business needs.
    $123k-184.4k yearly15d ago

  • Principal Data Engineer - Manufacturing Analytics (REMOTE ELIGIBLE

    The Principal Data Engineer - Manufacturing Analytics is responsible to enhance efficiencies for the implementation of TIBCO Spotfire and Statistica to make the user experience seamless. At Vertex, our Total Rewards offerings also include inclusive market-leading benefits to meet our employe
    $108k-162k yearly15d ago

  • Director, Clinical Trial Management (Remote

    The Director, Clinical Trial Management is responsible for the planning, oversight, and execution of study and program-level deliverables across a range of study phases within one or more therapeutic areas to ensure corporate goals are met. This role often has responsibility for complex therapeutic areas with multiple compounds under simultaneous clinical development. This role will also manage a high performing global team of Clinical Trial Managers in the fast-paced and expanding Global Clinical Operations (GCO) organization, and may also manage individuals at the Associate Director level who also have program-level responsibilities. This position has a strong affiliation with the GCO Leadership Team and other senior stakeholders within Global Medicines and Development Affairs (GMDA). Key Duties and Responsibilities: * Represents GCO as a key Program Team member, responsible for the development and execution of clinical development plans in conjunction with the Program Teams. * Manages Clinical Trial Managers with responsibility for recruitment, resourcing, training, performance management, employee goal setting and career development. May also manage contract staff. * Develops operational strategy (study scenario planning, operational decision points and risks, initial study timeline, study financials) for assigned program(s). * Accountable for operational delivery of all clinical trials within program lifecycle, overseeing cross-functional alignment, budget, and timeline from protocol generation through completion of the clinical study report, ensuring quality and a focus on inspection readiness throughout. * Proactively identifies study and program risks and implements contingency plans, providing regular updates on study status to GCO Leadership Team and senior stakeholders in GMDA. * Participates in vendor identification and oversees Clinical Trial Managers in vendor set up and oversight. * Active involvement in investigator identification and selection, including the expansion to new geographies. * Provides oversight on the development of study documentation, including clinical trial protocols, study plans and clinical study reports. * Participates in cross functional study data review where appropriate. * Develops departmental goals and objectives for Clinical Trial Management. * Tracks key performance indicators and departmental metrics for Clinical Trial Management and identifies opportunities to optimize processes and procedures (SOPs, Work Instructions). * Leads cross-functional initiatives * Serves as representative for Clinical Trial Management on vendor-related Joint Operating Committees. Knowledge and Skills: * Demonstration of advanced project/program management skills including timeline and budget management, risk assessment and contingency planning. * Proven track record of successfully overseeing staff to execute and deliver clinical trials on time and on budget, ensuring inspection readiness throughout. * Excellent understanding of GCP, CFR and ICH Guidelines. * Effective team leadership in cross-functional study and program teams, with demonstrated strength in team building. * Significant experience with direct line management of employees. * Excellent verbal and written communication skills, organizational skills, problem solving and conflict resolution skills. * Strong interpersonal skills and demonstrated ability to effectively interface successfully with external parties, including key medical personnel at investigational sites, Key Opinion Leaders, vendors and Patient Advocacy groups. * Excellent presentation skills with ability to adapt communication and content appropriately based on the intended audience. * Self-motivated and proactive with ability to work independently in highly time sensitive environment. * Proficiency in Microsoft Office applications including Microsoft Project, Outlook, Excel, Word and PowerPoint. Education and Experience: * Bachelor's degree in life sciences discipline or related discipline * Typically requires 12 years of experience executing clinical trials globally across all phases of development and 3 years of supervisory/management experience, or the equivalent combination of education and experience. Pay Range $ 180,000 - 270,000 annually The range provided is based on what we believe is a reasonable estimate for the base salary pay range for this job at the time of posting. This role is eligible for an annual bonus and annual equity awards. Some roles may also be eligible for overtime pay, in accordance with federal and state requirements. Actual base salary pay will be based on a number of factors, including skills, competencies, experience, and other job-related factors permitted by law. At Vertex, our Total Rewards offerings also include inclusive market-leading benefits to meet our employees wherever they are in their career, financial, family and wellbeing journey while providing flexibility and resources to support their growth and aspirations. From medical, dental and vision benefits to generous paid time off (including a week-long company shutdown in the Summer and the Winter), educational assistance programs including student loan repayment, a generous commuting subsidy, matching charitable donations, 401(k) and so much more. #LI-JM1 #LI-Remote Company Information Vertex is a global biotechnology company that invests in scientific innovation. Vertex is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, sex, gender identity or expression, age, religion, national origin, ancestry, ethnicity, disability, veteran status, genetic information, sexual orientation, marital status, or any characteristic protected under applicable law. Vertex is an E-Verify Employer in the United States. Vertex will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law. Any applicant requiring an accommodation in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should make a request to the recruiter or hiring manager, or contact Talent Acquisition at ApplicationAssistance@vrtx.com.
    $180k-270k yearly15d ago

  • Vendor Master Specialist - Accounts Payable (Remote

    Overview: The Vendor Master Specialist role reports to the Accounts Payable Manager, and will be responsible for the onboarding and maintenance of supplier records within the Vertex supplier database. Duties may also include a review of the onboarding process and policy and provide feedback, testing, and backup of Vertex's international team, when necessary, as well as other Accounts Payable tasks. At Vertex, our Total Rewards offerings also include inclusive market-leading benefits to meet our employees wherever they are in their career, financial, family and wellbeing journey while providing flexibility and resources to support their growth and aspirations.
    $52k-78k yearly32d ago

  • Director, Clinical Science (remote

    * Represents Vertex to outside personnel in the development of clinical protocols and study conduct The Director, Clinical Scientist will work as the key clinical interface to provide scientific, clinical, and operational input to early and late stage clinical development programs, with an emphasis on program strategy activities.
    $184.3k-276.5k yearly9d ago

  • Senior Administrative Coordinator

    + Ability to discern and communicate with the highest level of tact and diplomacy, both verbally and in writing to members of the Board of Directors, the Steering Committee, industry and government officials, analysts, Alexion clients and all levels of the organization. At Alexion, people living with rare and devastating diseases are our Guiding Star. The Administrative Coordinator will be responsible for the coordination of activities (operations and planning) and ensuring timely flow of information to and from the executive office, supporting the SVP of Strategy & Business Developement for the Rare Disease Unit in Boston, MA!
    $83k-112k yearly est.49d ago

  • Senior Manager, Medical Affairs Technologies

    The Senior Manager, Medical Affairs Technologies is responsible for providing business analysis and subject matter knowledge to medical affairs technology implementation teams. At Alexion, people living with rare and devastating diseases are our Guiding Star.
    $131k-165k yearly est.60d ago

  • Senior Manager, Strategic Sourcing (Remote

    * Manages the Supplier Performance/Relationship Management process that may include Executive Business Reviews that include Senior leaders both within Vertex and with the 3rd party.
    $127k-168k yearly est.17d ago

  • Director, Global Health Economics and Outcomes Research

    * Delivers presentations on behalf of Alexion at various industry and scientific forums and/or contribute to publications * Cultivates and maintains relationships with key experts, influencers, and customer segments to foster and maintain Alexion's credibility to support the value and reimbursement of Alexion products The Director, Global Health Economics and Outcomes Research (GHEOR) leads the strategic development and execution of health economics and outcomes research strategies to support the worldwide launch and reimbursement of products across a range of multiple disease areas, assets, and indications. At Alexion, people living with rare and devastating diseases are our Guiding Star. This collaboration builds strategies to demonstrate and differentiate the value proposition and corresponding scientific evidence of Alexion products for payers, patients, clinical institutions, and other key influencers. Ensures Alexion maintains external credibility and relationships to validate research findings and communications.
    $126k-172k yearly est.16d ago

  • Regulatory Publishing Manager (Remote

    At Vertex, our Total Rewards offerings also include inclusive market-leading benefits to meet our employees wherever they are in their career, financial, family and wellbeing journey whi The Regulatory Publishing Manager will be responsible for contributing to process improvements for the accurate and quality driven execution of submissions. The Regulatory Publishing Manager is responsible for the creation, assembly, and publishing of electronic submissions and the delivery to global health authorities in an efficient and timely manner. 3. Remote and work remotely with occasional travel to Vertex sites for business critical meetings/events.
    $168k yearly31d ago

  • Director, Audit Management, Cell and Gene Therapy (Remote

    The Director, Global Compliance Cell and Gene Therapy (CGT), as part of the Global Quality Compliance group within the Vertex Quality Assurance Organization, is responsible for risk based GMP/GDP auditing and compliance programs for CMC CGT platform of products. Vertex is an exciting, fast paced dynamic environment with a strong company culture focused on patients with unmet medical needs. This individual will be responsible for design and execution of risk-based approaches related to the audit of CMC activities, conducted both internal to Vertex and at their respective CDMOs/distributors, assuring adherence to applicable regulations, industry standards, and to Vertex policies, procedures and quality standards as set forth in the Quality Management System. This position leads a team of compliance experts' oversight of key Vertex CMC activities regulated by international regulatory bodies, while continuing to work closely as liaisons with Quality Operations and key business partners globally.
    $173.6k-260.4k yearly44d ago

  • Manager, Digital Experience

    In alignment with strategic business goals, this individual will enable future growth of the company by helping to implement and institute digital capabilities in support of the Alexion business globally. At Alexion, people living with rare and devastating diseases are our Guiding Star. + Establish collaborative relationships within Alexion Technology Services team to ensure the seamless delivery of new technologies and maintain an ongoing support model The Digital Experience (DEX) team is growing and looking to hire a Manager, Digital Experience to join their team.
    $97k-132k yearly est.10d ago

  • Senior Manager, Development and Safety Operations

    At Alexion, people living with rare and devastating diseases are our Guiding Star. Alexion is a global biopharmaceutical company focused on serving patients and families affected by rare diseases and devastating conditions through the discovery, development and commercialization of life-ch * Budget Management: Manages Development & Safety's functional budget and serves as primary representative to key stakeholders within Alexion.
    $129k-165k yearly est.56d ago

  • Director, Global Value, Access, and Pricing, Complement Lead

    Alexion, AstraZeneca's Rare Disease Business Unit, is seeking a qualified Director to be part of the dynamic and growing Global Value, Access, and Pricing (GVAP) team with responsibility for the development of global pricing and reimbursement (P&R) strategies and integrated value platforms for its Complement assets across multiple indications in chronic and acute care settings. At Alexion, people living with rare and devastating diseases are our Guiding Star. * Develop global pricing recommendations for Alexion's assets * Lead and manage efforts to analyze, synthesize and translate developments and challenges in the P&R landscape globally into meaningful decision points, recommendations, strategies and tactics for Alexion's products and assets The Director will represent the GVAP function at the relevant Global Program Teams / Global Launch Teams as well as other cross functional global teams and will be an integral partner with the VISion team. The Director will be responsible for the development and execution of P&R strategy and activities, incorporation of both acute and chronic indications in C5 portfolio as well as future potential assets & indications. The Director will be located in Alexion's Boston office.
    $158k-210k yearly est.21d ago

  • Project Management Associate Director, Publications (Remote

    The Project Management Associate Director will be responsible for the integration, creation and execution of multiple complex departmental development plans within the Publications group. The incumbent is held accountable for project development and timelines and serves a resource for other team members and Vertex departments.
    $91k-119k yearly est.10d ago

  • Bioinformatics Data Engineer/Scientist I

    Alexion is a global biopharmaceutical company focused on serving patients and families affected by rare diseases and devastating conditions through the discovery, development and commercialization of life-changing medicines. As an integral part of Alexion's Bioinformatics and Data Sciences team you will create and apply novel data engineering solutions spanning the fields of Early Discovery, Target Identification/Validation, Translational Medicine, Clinical Development and Diagnostics, with the overall goal of advancing Alexion's rare disease portfolio and to better identify rare disease patients. You will join a highly skilled team which prides itself on creating strategic value and catalyzing change across Alexion through the innovative application of data sciences. Headquartered in Boston, Massachusetts, Alexion has of You will need to effectively collaborate with other colleagues at Alexion with diverse scientific backgrounds to deliver novel quantitative solutions and analyses. At Alexion, people living with rare and devastating diseases are our Guiding Star.
    $98k-125k yearly est.49d ago

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Updated June 5, 2023