IQVIA

Manager

• You promote scientific exchange as well as professional dialogue and collaboration with office-based physicians, hospital physicians and other external stakeholders
• You lead scientific discussions, deliver presentations, communicate data and give scientific talks
• You establish and maintain your network of external medical-scientific experts and key opinion leaders (KOLs)
• You provide medical information and answer complex medical and scientific questions and inquiries
• You support internal teams with your medical-scientific expertise and conduct trainings
• You coordinate scientific educational activities and actively participate in events such as advisory boards, congresses and medical education formats
• You gather relevant information on current developments in your therapeutic area

Medical Science Liaison Manager – Vaccines

• Du förderst den wissenschaftlichen Austausch sowie den fachlichen Dialog und die Zusammenarbeit mit niedergelassenen Ärzten, Klinikärzten und weiteren externen Stakeholdern
• Du führst wissenschaftliche Diskussionen, Präsentationen, die Vermittlung von Daten und fachlichen Vorträgen durch
• Du etablierst und pflegst dein Netzwerk aus externen, medizinisch-wissenschaftlichen Experten und Meinungsbildnern
• Du stellst medizinische Informationen bereit und beantwortest komplexe medizinische und wissenschaftliche Fragestellungen und Anfragen
• Du unterstützt interne Teams mit deiner medizinisch-wissenschaftlichen Expertise und führst Schulungen durch
• Du koordinierst wissenschaftliche Fortbildungsaktivitäten und nimmst aktiv an Veranstaltungen wie Advisory Boards, Kongressen und medizinischen Fortbildungsformaten teil
• Du sammelst relevante Informationen zu aktuellen Entwicklungen im Therapiegebiet aus deinem Gebiet

Medical Science Liaison Manager – Impfstoffe

• You promote scientific exchange as well as professional dialogue and collaboration with community-based physicians and hospital clinicians.
• You lead scientific discussions, presentations, and lectures.
• You establish and maintain your network of external medical-scientific experts.
• You provide medical information and answer complex medical and scientific inquiries.
• You support internal teams with your medical-scientific expertise.
• You coordinate scientific continuing education activities and actively participate in events.
• You gather relevant information on current developments in the therapeutic area.

Solutions Engineer

• Architect and deliver scalable, secure cloud-native systems across AWS and Azure.
• Lead architecture for AI-enabled and agentic applications, including LLM-based workflows.
• Rapidly build MVPs and prototypes to validate requirements and architectural decisions.
• Use AI-assisted development tools (e.g., Cursor) to accelerate prototyping and iteration.
• Engage stakeholders to define requirements, trade-offs, and architectural direction.
• Provide architectural guidance and mentorship across teams, serving as a collaborative partner to Tech Leads by working jointly on architectural direction and project delivery while offering hands-on support as needed.

AI Solution Architect

Research Analyst

• Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required.
• Perform site monitoring visits in accordance with contracted scope of work and regulatory requirements.
• Work with sites to adapt, drive, and track subject recruitment plan in line with project needs.
• Administer protocol and related study training to assigned sites and establish regular lines of communication with sites.
• Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol.
• Escalate quality issues as appropriate.
• Manage the progress of assigned studies by tracking regulatory submissions and approvals.
• Ensure copies/originals of site documents are available for filing in the Trial Master File (TMF).

Senior Clinical Research Associate

Program Manager

• Responsible for manufacturer program operations and client relationship.
• Supervise and coordinate daily workflow with leadership.
• Understand and coordinate all patient assistance program requirements with appropriate departments.
• Examine metrics and reporting daily for all program activity and ongoing trending.
• Facilitate data requirements between clients and third parties.
• Facilitate communication and collaboration for all program changes and updates between all departments.
• Responsible for program specific SOP management and documentation processes.
• Assist with program change requests for PRM updates.
• Present on demand data to Executive Team as requested.
• Demonstrate a high aptitude for learning about the specialty pharmacy healthcare environment.
• Provide communication and follow-up to ensure staff are fully informed of all new information related to products, procedures, customer needs, and company related issues, changes, or actions.
• Responsible as program SME at business reviews.
• Responsible to continuously look for ways to improve program.

Associate Director, Program Management – Patient Support Services

• Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.
• Perform site monitoring visits (selection, initiation, monitoring, and close-out visits) in accordance with contracted scope of work and Good Clinical Practice.
• Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability.
• Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.
• Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate.
• Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase.
• Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements.
• Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.
• Collaborate and liaise with study team members for project execution support as appropriate.

Compliance

• ローカルでの品質・コンプライアンスを支えるポジションです。
• 新入社員のオンボーディング支援や、QMS/GCPに関する相談対応、ローカル規制情報の更新などを担当します。
• 品質・コンプライアンス管理
• コンプライアンスリスクの監視と、必要な是正/予防措置(CAPA)の策定
• 是正計画の進捗確認と、QCチェック・特別調査による効果検証
• 四半期ごとの品質レビューへの参加
• 査察・監査が円滑に進むよう、国内外の関係部署と連携
• QEMにおけるCAPA支援や、研修・アカウント管理などの地域リード業務
• ローカル手順書(SOP等)の作成・管理
• TMF(治験マスターファイル)のQCチェック、On-Site Compliance Monitoring Visits の実施
• GCOコンプライアンスに関するオペレーションプロジェクトのサポート
• オンボーディング・相談窓口業務
• 新入社員のオンボーディングサポート
• QMSやコンプライアンス研修・ワークショップの企画と運営
• SOP、システム、GCPに関する専門的アドバイスの提供
• 国レベルでのリスク分析とリスク低減策のアドバイス
• ローカル規制インテリジェンス
• 新規・改訂された現地規制の影響評価
• RIACS、T‑Race、IRON などのローカル情報を最新に保ち、中央機能をサポート
• Business Quality との連携による LOC マネジメントレビューやローカルサプライヤー評価の支援

Senior Local Compliance Specialist

• The Global Study Manager is a member of the extended global study team supporting delivery of clinical studies within BioPharmaceuticals Clinical Operations, Study Management to time, cost and quality, from Clinical Study Protocol (CSP) development through study set-up, maintenance, close-out, development of Clinical Study Report (CSR) to study archiving.
• Leads/contributes to the preparation of delegated study documents (e.g., Informed Consent Form, master Clinical Study Agreement etc), and external service provider related documents (specifications, study specific procedures, descriptions, presentations etc.).
• Maintains and facilitates interactions with internal functions and external functions including the CROs and other external service providers to ensure an efficient study delivery to time, costs and quality objectives.
• Contributes to the planning and conduct of internal and external meetings (e.g., Investigators’/Monitors’ meeting).
• Ensures the supply of Investigational product and study materials by liaising with Clinical Supply Chain or external service providers as appropriate.
• Proactively contributes to risk and issue identification, development of mitigation and/or action plans for identified risks and issues.
• Ensures that all study documents in scope of GSM’s responsibilities are complete and verified for quality in Trial Master File.
• Supports GSD and/or GSAD with budget management, such as external service provider invoice reconciliation.
• Adheres to global clinical processes, procedural documents, applicable Quality & Compliance manual documents and international guidelines such as ICH/GCP to ensure study is inspection ready at all times.
• For outsourced studies, supports GSD and/or GSAD in management of the CRO Project Manager to ensure study delivery according to agreed timelines, budget and quality standards, while ensuring that the appropriate level of oversight of the CRO is maintained and documented throughout the lifecycle of the study.

Global Study Manager – Sponsor Dedicated

• Leading the delivery of the IR offer for key HQ clients in EMEA, deploying the right delivery resources and innovation to ensure repeat and new business is generated from major accounts
• Understanding clients’ needs and developing high quality proposals to address those
• Bringing strategic thinking to client issues, developing clear actions for the client to solve their issues and acting as the trusted advisor to clients on a project basis
• Ensuring that offering development is scalable across different client business issues
• Design research solutions, including identification of relevant data assets, methodology, samples, questionnaires, discussion guides and other research tools
• Taking a leadership role in implementing B&IRS business vision and objectives, and support the development of the business
• Coaching offshore team and more junior team members
• Taking responsibility for a significant part of the business, achieving revenue targets
• Managing end to end consulting and Primary Market Research projects including coordination of multidisciplinary teams staffed to the project, such as fieldwork, programming and desk research

Engagement Manager – Integrated Research

• Perform tasks at a country level associated with Site Activation (SA) activities
• Serve as Single Point of Contact (SPOC) in assigned studies for investigative sites
• Ensure adherence to standard operating procedures (SOPs)
• Prepare site regulatory documents, reviewing for completeness and accuracy
• Review and provide feedback to management on site performance metrics

Regulatory and Start Up Specialist

Medical Director

• Provide medical, clinical and scientific advisory expertise
• Serve as a Global Medical Advisor on assigned projects
• Medical support to sites and project staff for protocol-related issues
• Attend and present at Investigator Meetings

Associate Medical Director – Oncology, Sponsor-Dedicated, Fixed Term Contract

Customer Support

• Build strong relationships with our customers and legal counsel
• Track progress of Agreements with client Legal counsel and BSCI Legal counsel
• Follow up to ensure agreements are progressing through the review and approval process
• Manage and track status of BAAs
• Create, maintain, and recommend enhancements to policies and procedures
• Track, analyze, and interpret metrics related to BAA process
• Provide broad troubleshooting support for field teams
• Create how-to documents and work instructions
• Coordinate with Health Care Professionals and legal counsel

Marketing Support Specialist

Sales

• This position works closely with cross functional peers, in a collaborative environment, to ensure that the company suite of services is made available as appropriate.
• You must be able to combine strong clinical and interpersonal skills to establish yourself as a trusted partner.
• Through probing define the patient’s unmet needs and align on solutions, compliantly and within the company framework that exceeds customer expectations.
• Work virtually when necessary, making outbound calls developing relationships and building trust with key providers and staff.
• Educating stake holders using all available virtual tools.
• Successful experience working Teaching Institutions, major hospitals, large oncology clinics, groups, and or accounts.
• Request, organize and attend relevant oncology conferences which may occur on weekends.
• Appropriately utilize all company approved marketing tools and resources, including digital presentations, use selling skills framework to advance in the selling cycle (i.e., another appointment, in-service, patient identification, etc.).
• Develop customer specific pre- and post-call plans that include objectives, probes, and supporting approved materials.

Oncology Overlay Sales Specialist

Account Executive

• Driving volume and market share growth for assigned pharmaceutical products
• Building strong relationships with healthcare professionals
• Delivering impactful sales presentations

Medical Science Liaison Manager – Vaccines

Medical Science Liaison Manager – Impfstoffe

Medical Science Liaison Manager – Vaccines

AI Solution Architect

Senior Clinical Research Associate

Associate Director, Program Management – Patient Support Services

Senior Clinical Research Associate

Senior Local Compliance Specialist

Global Study Manager – Sponsor Dedicated

Engagement Manager – Integrated Research

Regulatory and Start Up Specialist

Associate Medical Director – Oncology, Sponsor-Dedicated, Fixed Term Contract

Marketing Support Specialist

Oncology Overlay Sales Specialist

Pharmaceutical Sales Representative – GI