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BeiGene
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  • Key Account Manager, UK  

    BeOne continues to grow at a rapid pace with challenging and exciting... Read More
    BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our passionate interest in fighting cancer.Company Overview:General Description:Territory to cover: South West England & South Wales
    A great opportunity to join BeOne in an early stage of its growth. We are looking for a truly passionate and empathic individual with a track record in Haematology/Haem-Onc and with extensive knowledge of local and regional healthcare systems.You love to engage with stakeholders at all levels to ensure BeOne and our treatments are well known and appreciated and to help give patients the possibility to benefit from our innovative treatments. The Key Account Manager (KAM) implements the sales strategy in the area and is responsible for achieving defined sales targets within an agreed expense budget. In addition, the KAM supports and advises the key account customers in the territory in an appreciative, open-minded, and honest manner.Essential Functions of the job:Develop and execute strong regional plans with cross-functional support. The objective is to build customised regional stakeholder engagement plans that drive best-in-class service, engagement, and impact.Using expertise in haem-oncology be a go-to scientific and patient care resource for stakeholders in the assigned region.Collaborate with health system partners, health care practitioners (HCP), regional patient advocacy groups, and relevant stakeholder groups in the region to support best-in-class haeme-oncology care and education with the patient always at the center.Building a BeOne image/brand and awareness for our company and our products in the haematology-oncology market in the served areaPlan, identify, analyse, and implement activities and meetings to optimise regional potentialResponsible to ensure that the target customers are updated on our product strategy and communication, including regional budget holders to generate/validate payor projects and solution.Collaborate with regional Key Opinion Leaders, Head of Clinics and Expert/Therapy group members and prescriber target groups.Scientific expert advice and support of opinion leaders and medical haemato-oncologists in hospitals and private clinicsResponsibility for the regional sales goals and qualitative performance parameters, as agreed with the managerDevelopment, implementation, and execution of projects to optimize patient care in collaboration with our key customers: Use and apply in suitable situations the Project Management to cooperate and develop the Key Account CustomersOrganization and execution of local symposia, educations and workshops with the key customersBroad understanding of regional processesParticipation and customer care in local, national, and international meetings and symposiaEnsure compliance within all activities to maintain the highest standards of patients focused ethical conduct in line with our values.Consistently ensure operating in accordance with BeOne´s Standards of conduct and all applicable local laws and regulations.QualificationsLife science degree (university, college) or equivalent professional experienceSeveral years of qualified work experience as commercial representative, preferably in the haemato-oncology marketScientific education and experiences in this or similar positionsSpecific knowledge in haematology-oncology and distinct knowledge in project management is desirableStrong identification with BeOne´s values and loyalty to the companyWillingness to learning and continuously developing (trainings and coaching’s)Demonstrated success in a small but fast growing, entrepreneurial commercial environment is desirableMaking things happen, has the right level of implementation skillsMarketing and commercial-oriented thinking and workingExcellent reliable contacts with opinion leaders in the relevant indications (special knowledge in the field of Lymphomas) is desirableKnowledge of the regional budget processes and distribution structuresHigh social competence and capacity for teamworkHighly motivated, solution oriented and a positive attitudeHigh social competence and capacity for teamworkSuccess-, service-, and commercial oriented thinking and workingGood English and computer skillsWillingness to travelValid driver‘s licenseGlobal CompetenciesWhen we exhibit our values of Patients First, Driving Excellence, Bold Ingenuity, and Collaborative Spirit, through our twelve global competencies below, we help get more affordable medicines to more patients around the world.Fosters TeamworkProvides and Solicits Honest and Actionable FeedbackSelf-AwarenessActs InclusivelyDemonstrates InitiativeEntrepreneurial MindsetContinuous LearningEmbraces ChangeResults-OrientedAnalytical Thinking/Data AnalysisFinancial ExcellenceCommunicates with Clarity Read Less
  • Principal Medical Writer  

    - Cambridge
    BeOne continues to grow at a rapid pace with challenging and exciting... Read More
    BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our passionate interest in fighting cancer.BeOne Medicines USA, Inc. seeks Principal Medical Writer in Cambridge, MA:
    Job Duties: Responsible for providing expertise to support the development of high-quality, fit-for-purpose clinical and regulatory documents to facilitate speed of information during development, submission, approval, and life-cycle management of products in BeiGene pipeline. Also responsible for mentoring junior MWs (full-time employees and/or contractors/vendors) as needed. Manage multiple documents at the same time, including the complex documents (eg, those with complex content, urgent timeline, or external collaboration). Contributes to direction and strategy setting (including critically analyzing, synthesizing, and presenting complex information) for document development in collaboration with study team(s). Contribute to the creation and maintenance of document writing template/guidance for the document types listed in the General Description part. Lead part of the maintenance of document writing template/guidance for the document types listed in the General Description part. Identify the questions/issues that require departmental discussion or team discussion with guidance from line manager/mentor. Identify the potential risks and make a mitigation plan with guidance from line manager/mentor. Resolves problems with guidance from line manager/mentor (eg, takes concrete actions according to the aligned decisions). Understands the role of own documents within the larger dossier and voices out any impact on upstream and downstream processes. Provide technical and operational mentorship to junior MWs (full-time employees and/or contractors/vendors). Understands the global MW scope and works to guide study team(s) and program team(s) within the defined scope and responsibility following established processes. Provides topic sharing on regulatory writing and related knowledge within the department and across the company (and to cross-functional stakeholders with guidance from line manager/mentor). Full-time telecommuting is an option.
    Minimum Requirements: PhD (or its foreign degree equivalent) in Biotechnology, Engineering (any field), Biochemistry, or a related quantitative discipline, and 2 years of experience in the job offered or in any occupation in related field, OR Master’s degree (or its foreign degree equivalent) in Biotechnology, Engineering (any field), Biochemistry, or a related quantitative discipline, and 5 years of progressively responsible experience in the job offered or in any occupation in related field.Special Skill Requirements: Writing clinical study reports;Writing protocols;Writing protocol amendments;Analyzing, Synthesizing, and Presenting Complex Information utilized in Medical Documentation;Working with regulatory authorities from multiple regions. Any suitable combination of education, training and/or experience is acceptable.Full-time telecommuting is an option.Disregard the below range, the selected candidate will earn a wage of $137,100 - $171,400 per annum.
    Submit resume with references to: Req.#: L24-150320 at: ATTN: Amy Nobriga, #LI-DNIGlobal CompetenciesWhen we exhibit our values of Patients First, Driving Excellence, Bold Ingenuity and Collaborative Spirit, through our twelve global competencies below, we help get more affordable medicines to more patients around the world.Fosters TeamworkProvides and Solicits Honest and Actionable FeedbackSelf-AwarenessActs InclusivelyDemonstrates InitiativeEntrepreneurial MindsetContinuous LearningEmbraces ChangeResults-OrientedAnalytical Thinking/Data AnalysisFinancial ExcellenceCommunicates with ClaritySalary Range: $119,300.00 - $159,300.00 annuallyBeOne is committed to fair and equitable compensation practices. Actual compensation packages are determined by several factors that are unique to each candidate, including but not limited to job-related skills, depth of experience, certifications, relevant education or training, and specific work location. Packages may vary by location due to differences in the cost of labor. The recruiter can share more about the specific salary range for a preferred location during the hiring process. Please note that the listed range reflects the base salary or hourly range only. Non-Commercial roles are eligible to participate in the annual bonus plan, and Commercial roles are eligible to participate in an incentive compensation plan. All Company employees have the opportunity to own shares of BeOne Medicines Ltd. stock because all employees are eligible for discretionary equity awards and to voluntarily participate in the Employee Stock Purchase Plan. The Company has a comprehensive benefits package that includes Medical, Dental, Vision, 401(k), FSA/HSA, Life Insurance, Paid Time Off, and Wellness. Read Less
  • Senior Manager, IT Audit  

    - Cambridge
    BeOne continues to grow at a rapid pace with challenging and exciting... Read More
    BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our passionate interest in fighting cancer.General Description: BeiGene is seeking an experienced Senior IT Audit Manager to join our growing internal audit (IA) function, who will be responsible for IA assurance activities from a business, technology, and security perspective across the organization. This person will support the achievement of the Company’s business objectives by bringing a systematic, disciplined approach to evaluate and improve the effectiveness of the company’s risk management, control, and governance processes related to technology areas. This position will liaise across business groups, including but not limited to IT, Finance, Legal, Compliance, external auditors, and other stakeholders to execute the Internal Audit Plan and SOX 404 assurance work.Essential Functions of the job: Strategic Business Partnership and Risk AssessmentSupport Associate Director, IT Audit toDevelop and maintain strategic partnerships to improve risk management and control processes.Engage in the risk assessment process by identifying and evaluating technology-related risks that could affect the achievement of business objectives, ensuring alignment with company goals.Implement and maintain risk management strategies for Internal Audit, monitor and report on risk status, ensure compliance with regulations, and collaborate with internal control teams to maintain a robust IT environmentAudit LeadershipLead complex and/or global financial, compliance, and operational audits and advisory initiatives to assess process and control effectiveness, encompassing all audit cycle phases: planning, execution, issue escalation, documentation, reporting, and remediation follow-up.Develop risk-based, tailored audit programs across a wide variety of IT risks, including but not limited to areas such as Cybersecurity, System Implementations, Data Privacy, Active Directory, etc.Conduct on-site fieldwork to assess the Company’s information system and security related processes and controls. Ensure all audit program steps are completed, transactions are thoroughly evaluated, and work papers are properly documented for audit conclusions.Craft accurate, concise and compelling audit and advisory reports, and support or deliver presentations of findings and recommendations to internal and external management, including senior leadership.Coordinate with external auditor and management in leading the annual planning of Sarbanes-Oxley (SOX) 404/C-SOX compliance requirements.Collaborate with co-source and external auditors to support global Sarbanes-Oxley 404 compliance by assessing and testing ITGC and ITAC internal controls, ensuring adequate test work, documentation, and audit quality to drive more reliance.Coordinate and collaborate with business leaders, external auditors, and other control and monitoring disciplines (i.e., IT, Compliance and Legal) to facilitate audits and ensure effective and efficient coverage of Company-wide risks.Project ManagementAllocate resources for internal audits and manage third-party work to ensure timely and high-quality completion.Monitor audit projects proactively, addressing issues promptly to ensure smooth progress.Ensure all audit activities comply with internal audit standards and methodologies, maintaining rigor and professionalism.
    Additional AssignmentsSupport any additional assignments or special projects as required including but not limited to Quality Assurance and Improvement Program (QAIP), External/Internal Quality Assessment to enhance the effectiveness and efficiency of the Internal Audit function.Stay updated on industry trends and best practices in internal auditing and relevant subject matter expertise areas.Supervisory Team DevelopmentProvide coaching and mentoring to team members on audit projects, ensuring they develop the necessary skills and knowledge to excel in their roles.Cultivate a collaborative and supportive team environment, promoting open communication, mutual respect, and a shared commitment to achieving audit objectives.Identify the developmental needs of team members and facilitate targeted training opportunities, foster continuous professional growth and enhance overall team performance.Computer Skills:  Strong Microsoft Office skills (particularly Excel and PowerPoint)Knowledge of various operating systems like Windows, Linux, and Unix.Understanding of database management systems such as SQL, Oracle, and NoSQL databases.Familiarity with network infrastructure, protocols, and security measures.Proficiency in audit software tools like AuditBoard, ACL, Tableau, PowerBI and other data analytics toolSkilled users of SAP and Generative AIEducation Required: Bachelor’s degree in computer science, Management Information Systems, Cybersecurity, or related field of study from an accredited universityOther Qualifications: 7-12 years of progressive experience in performing and independently leading complex information technology and cybersecurity audits. (Big Four Experience Preferred)Expert knowledge across all IT domains including cloud security, DevOps, secure software development, application security, databases, and operating systems,Expert knowledge of authentication, authorization, and credential managementStrong SOX/C-SOX ITGC and application control testing audit experience, and proficient in COSO, NIST CFS, ISO27001 etc. Standards.Strong verbal and written communication skillsProfessional Certification, (e.g. CISA, CRISC, CISSP, IAPP, CISM,) required; CIA preferred.Pharmaceutical industry experience and knowledge preferredTravel/Other Requirements: 10%, as requiredAvailability to meet during flexible hours on zoom/conference calls with colleagues in different U.S. time zones, Europe, and China.Global CompetenciesWhen we exhibit our values of Patients First, Driving Excellence, Bold Ingenuity and Collaborative Spirit, through our twelve global competencies below, we help get more affordable medicines to more patients around the world.Fosters TeamworkProvides and Solicits Honest and Actionable FeedbackSelf-AwarenessActs InclusivelyDemonstrates InitiativeEntrepreneurial MindsetContinuous LearningEmbraces ChangeResults-OrientedAnalytical Thinking/Data AnalysisFinancial ExcellenceCommunicates with ClaritySalary Range: $129,400.00 - $174,400.00 annuallyBeOne is committed to fair and equitable compensation practices. Actual compensation packages are determined by several factors that are unique to each candidate, including but not limited to job-related skills, depth of experience, certifications, relevant education or training, and specific work location. Packages may vary by location due to differences in the cost of labor. The recruiter can share more about the specific salary range for a preferred location during the hiring process. Please note that the listed range reflects the base salary or hourly range only. Non-Commercial roles are eligible to participate in the annual bonus plan, and Commercial roles are eligible to participate in an incentive compensation plan. All Company employees have the opportunity to own shares of BeOne Medicines Ltd. stock because all employees are eligible for discretionary equity awards and to voluntarily participate in the Employee Stock Purchase Plan. The Company has a comprehensive benefits package that includes Medical, Dental, Vision, 401(k), FSA/HSA, Life Insurance, Paid Time Off, and Wellness. Read Less

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Astrid-Lindgren-Weg 12 38229 Salzgitter Germany