Gehaltsübersicht für Clinical Data Manager in Basel-Stadt

Your responsibilities will be but not limited to:Planing and developing the Medical Affairs strategy and executing Medical Affairs activities and scientific projects based on the medical strategy in close collaboration with other medical team members.Leading the development and delivery of medical education activities, both externally and internally, in close collaboration with the rest of the Medical teamDesigning and executing evidence generation efforts (e.g., publications, congress presentations) in close collaboration with other departmentsEstablishing and maintaining strong working relationships with external medical experts, including academic societiesPlaning and conducts Advisory Boards as needed to obtain insights.Presenting scientific and clinical data Experience:University degree in life-sciences. MD or PhD preferred.Min 8 years of experience in a similar positionExperience in rare diseases Strong ability to work in cross-functional teamsEntrepreneurial spirit with ability to adapt to a fast-changing environment  

 Your responsibilities will be but not limited to:Clinical trial material (CTM) label review and approval and assisting with CTM forecasting.Proactively identifying and resolving operational issues/processes to ensure achievement of study milestones, data quality and data integrity; escalates study-related issues appropriately in a timely manner.Participating in data cleaning, listing, and report output reviews.Developing, reviews, and approves study-related manuals, plans, specifications, charters, newsletters, and materials.Protocol deviation listing reviews and meetings.Responsible for oversight of study budget, investigator and vendor contracts, budgets and payments.Protocol, table, figure, data listings and clinical study report reviews. Experience:University degree in life-sciencesMin 5 years of experience in a similar position in phase IIIExperience in rare diseases  

The perfect candidate is someone who has done a similar position in bioanalysis previously within a pharma (preferred) or a CRO or an experienced scientist with experience with small and/or large molecules very keen to learn and with a positive attitude. Please note the preference goes to the first profile (experience in pharma/CRO). In any case, the successful candidate will have an education within biology / biochemistry. On this position, the perfect candidate has strong experience on both small AND large molecules. This is a long-term contract with a potential internal opportunity afterwards.  Tasks & Responsibilities:Lead bioanalytical strategies to generate decision-enabling bioanalytical data with skilled data interpretation to meet and answer project needsResponsible for outsourcing activities in Bioanalytics (bioanalysis of non-clinical and clinical studies); resource and time planning, coordination and administrative management of studies with CROs.Manage the development, transfer and validation of specific and sensitive bioanalytical methods required for the development compound (drug), anti-drug antibodies (ADA), soluble targets and any concomitant/interaction compound in the given project.Manage and direct analysis of samples and timeline from preclinical and clinical studies for the project at CRO labs.Participate actively in PS subteams, act as primary contact person for DMPK project leader.Act as Bioanalytical Leader when required. Interact proactively with the assay development team.Ensure full compliance with the current global and local bioanalytical guidance and GxPs.Leadership in Bioanalysis: *remain current and continually develop expertise in bioanalytical science. Contribute to scientific consortia when required; *maintain current expertise in the validation and conduct of bioanalytical assays; *guide and manage the bioanalysis at CROs and ensure that most advanced and most efficient procedures are used.Provide technical leadership in issue resolution.Review protocols and other relevant documents and guide project teams in all aspects of bioanalytical work required for the project.Review and write reports for regulatory submissions; support filings and answer any questions about bioanalytics coming from the regulatory agencies.Maintain open links with other disciplines within the department and the organization.Advise Group Head concerning all needs relating to administrative processes, technologies and equipment. Inform him of all critical issues Must haves:Minimum 3 years in a similar position focused on bioanalysis in pharma or CRO (pharma preferred) OR scientist focused on bioanalysis Excellent work experience on both large and small molecules bioanalysis Strong vendor management experience, looking after outsourced studies to external CROsDegree in biology/biochemistry  

BeiGene 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: Accountable for regional study delivery with appropriate inspection readiness quality, within agreed timelines and budget Leads the regional clinical operations team (including oversight of external partners working on the regional level) and acts as point of escalation for resolution of issues within the region for the assigned study Ensures alignment of regional deliverables with overall study goals Essential Functions of the job: Regional Leadership Leads the regional clinical operations team effectively, ensures effective decision making and acts as point of escalation for resolution of issues within the region for the assigned study Leads external vendors involved in study delivery on a regional level Collaborates with key stakeholders in the region and provides regular updates on study progress in the region to senior management and Global Clinical Study Manager as required Represents the regional study team at internal meetings and at the cross-functional Clinical Study Team (CST) meetings Leads regional operations meetings with all regional study team members Timelines, Planning and Execution Leads planning and management of the assigned clinical study(ies) from feasibility through closeout activities for region, in line with global study timelines Generates, manages, and maintains high quality study start up and recruitment timelines for region and tracks progress towards these Ensures that the clinical study is operationally feasible in the region, drives trial feasibility, country allocation and site selection process for assigned region in collaboration with feasibility managers, country heads, medical affairs and any other stakeholders Provides regional input on global study plans as required Ensures timely availability of local adaptations of global study documents such as informed consent forms, in close collaboration with other key stake holders to ensure timely submission to regulatory authorities and ECs/IRBs Accountable for submissions of study in countries in assigned region in close collaboration with regional study start up team and regulatory affairs Ensures regional and country information in study systems and tools is entered and up to date Collaborates closely with CRAs in the region to ensure proper study execution at the sites. Reviews and signs-off monitoring reports Responsible for working with regional and country teams to ensure that country and site level Trial Master File is created, maintained and QC’d on a regular basis as per the study TMF QC plan Provides input to Global Clinical Supplies regarding drug inventories in region and reviews local drug labels for region. Provides input on local regulatory approval and reimbursement status of comparator drugs used in study for countries in region Manages the trial data collection process for the region, drives data entry and query resolution As required, supports planning and execution of the Clinical Study Report in collaboration with Global Clinical Study Manager and Medical Writing Quality: Handles escalated issues or problems with the sites in region in close collaboration with stakeholders such as country heads Monitors study activities in region to ensure compliance with the study protocol, SOPs, ICH/GCP and all other relevant regulations Ensures inspection readiness for study in region at any point in time throughout the study life cycle Informs Global Clinical Study Manager of any issues arising on the study, evaluates impact and ensures solutions are implemented Prepares sites for quality assurance audits and inspections, drives responses to audit and inspection findings as appropriate Collaborates with CST members and colleagues to ensure cross-team, site learnings, and best practices are shared Leads improvements and partners with CST members to enhance the efficiency and the quality of the work performed on assigned studies Contributes to development, optimization and review of work instructions and SOPs as required Budget and Resources Works with the sourcing team to select and manage regional study vendors Manages regional study budgets Works closely with Clinical Business Operation on investigator fees, site payment issues and patient travel reimbursement activities Identifies and manages regional team resource needs and establishes contingency plans for key resources Monitors regional resource utilization over study life cyle and liaises with functional managers as needed Supervisory Responsibilities: Provides performance feedback on team members as required Might mentor junior team members Education Required: Bachelor’s Degree in a scientific or healthcare discipline required*, Higher Degree preferred *exceptions might be made for candidates with relevant clinical operations experience Competencies: Communicating Effectively Embracing Change Driving Excellence Working in Teams Mentoring Learning Computer Skills: MS Office, Project Planning Applications Other Qualifications: 4 or more years of progressive experience in clinical research within biotech, pharma or CRO industry Proven experience in clinical research including relevant experience as team lead in clinicial functions Experience as CRA is preferred Travel: Travel might be required as per business need BeiGene Global Competencies When we exhibit our values of Patients First, Collaborative Spirit, Bold Ingenuity and Driving Excellence, through our twelve global competencies below, we help get more affordable medicines to more patients around the world. Fosters Teamwork Provides and Solicits Honest and Actionable Feedback Self-Awareness Acts Inclusively Demonstrates Initiative Entrepreneurial Mindset Continuous Learning Embraces Change Results-Oriented Analytical Thinking/Data Analysis Financial Excellence Communicates with Clarity We are proud to be an equal opportunity employer and we value diversity. BeiGene does not discriminate on the basis of race, religion, color, sex, gender identity, sexual orientation, age, disability, national origin, veteran status or any other basis covered by appropriate law. All employment is decided on the basis of qualifications, merit, and business need. BeiGene is a global, commercial-stage, research-based biotechnology company focused on molecularly targeted and immuno-oncology cancer therapeutics. Currently employees are located in APAC, Americas, and Europe. BeiGene is advancing a pipeline consisting of novel oral small molecules and monoclonal antibodies for the treatment of cancer. BeiGene is working to create combination solutions aimed at having both a meaningful and lasting impact on cancer patients. For more information, see www.beigene.com. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. At BeiGene, how we work is just as important as the work we do. Below are our Values that determine the decisions we make and how we do things. Patients First Bold Ingenuity Collaborative Spirit Driving ExcellenceÜber das Unternehmen:BeiGene Switzerland GmbH

BeiGene 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: The Scientific Director, Solid Tumors, Medical Affairs will support BeiGene Clinical and Medical assets by successful execution of medical affairs programs and deliverables in partnership across the organization; with external vendors; and with external academicians and collaboration partners. The candidate will report to the VP Global Medical Affairs – Solid Tumors. The Scientific Director in Medical Affairs is responsible for actively participating in or driving pre- and post-marketing medical planning & execution of assigned medical affairs activities at BeiGene , with a focus on prelaunch and launch medical activities. This position will provide scientific and/or medical oversight by thoroughly understanding oncology / immuno-oncology and serving as a key scientific/medical resource. The Director will work in a multifunctional, matrix organization, working closely with colleagues within the medical affairs group (including field medical, medical operations, medical & product training, medical information, regional and global HEOR, publication management and bioanalytics), as well as those in research & development, commercial, access & reimbursement, and patient advocacy. He/she will also collaborate with external collaborators such as health care practitioners, research groups, payers and alliance partners. Essential Functions of the Job: Active contribution to Global Medical Affairs goals and ensures compliant execution of Global medical affairs activities. Co-develops annual Global Medical affairs Plans and oversight on development and execution of key regional or Country Medical Plans with VP of GMA medical Affairs and with Therapeutic Area Leads. Focus on pre-launch and launch related Global Medical efforts supporting regions, in particular Europe, U.S, LatAm, and MENA. Maintains deep scientific and medical knowledge of relevant therapeutic/disease areas as well as an understanding of patient & physician interactions to maintain acumen in clinical decision making. Responsible for medical affairs activities consisting of data generation, data analysis and interpretation. Plays a key role in developing evidence generation strategy and execution of Phase 3B/4 studies, including interventional and observational research. Provides strategic direction and scientific and medical support for publications and presentations as needed, working closely with Publication Manager(s). Evaluates investigator-initiated trial (IIT) applications. Review and input into publications including abstracts, posters, manuscripts Provides input and reviews of Medical Information Letters. Reviews and provides input into HEOR analyses Participates in scientific engagement with external groups in order to educate and advance scientific and medical understanding of relevant disease areas, including the management of disease, standards of patient care and roles of our assets. Develops and/or reviews medical content for congresses, symposia and advisory boards. Develop strategy for global external global medical education initiatives, as well as working on developing content, review of materials for global external medical education initiatives (company sponsored) Presents scientific/medical materials to diverse audiences (e.g., physicians, pharmacists, marketing/medical agencies, and other key stakeholders) in meeting, advisory and/or consulting settings. Provides scientific and medical input and ensures integrity of scientific content for promotional activities and sales training. May be the lead medical reviewer in the global review committee responsible for the review and approval of promotional, educational and related materials supporting Company products, ensuring medical/scientific accuracy and fair and balanced representation. Inclusive of Promotion and Medical materials for use with outside customers. Partners with country directors in all aspects of Medical Affairs activities to ensure their successful execution of their respective country medical plans and ensures alignment with Global Medical Plans. Coordinates with Project Management to ensure synergies between regions where applicable and proper development and utilization of Global Resources. Assesses medical education needs and assists in the development of internal and external educational activities with the Medical Affairs Director of Training. Works with finance, multiple functions with Medical Affairs and Project Manager to develop and forecast project budgets for medical affairs activities for responsible assets. Provides medical training for internal staff (including field medical, medical information, commercial, and sales) on products and disease related aspects, upon request. Required Education PharmD or Ph.D. with expertise in oncology / immuno-oncology Clinical research and/or drug-development knowledge and experience in oncology / immuno-oncology, required. Required Qualifications: Phd or PharmD with 5 plus years overall experience, 3 plus years experience in the pharmaceutical industry in Medical Affairs and and 2 plus years of experience in a relevant clinical practice is required. Working knowledge of applicable Federal and State Compliance guidelines and regulations required. Experience with internal Medical Affairs & Compliance related SOPs and policies required. Global Medical Affairs Experience preferred Experience with vendor selection and management preferred. Knowledge of industry standard Medical Services expected. Product launch experience is preferred. Capabilities and Competencies: Professional presence & demeanor. Values based collaborator – respectful, accountable and collaborative. Ability to relate and work with a wide range of people to achieve results. Impactful written and verbal scientific communication. Respectful and effective influencing skills. Confident, positive attitude, enthusiastic. Appreciation of diversity and multiculturalism. Strategic and creative thinker. Ability to build working relations throughout the organization and with business partners to achieve business goals within the Americas but also across multiple global regions, when necessary. Strong time management and organizational skills. Ability to manage multiple projects in a fast-paced environment. Skilled in multiple computer-based tools, in addition to software Ability to speak foreign language, preferred. Supervisory Responsibilities: N/A BeiGene Global Competencies When we exhibit our values of Patients First, Collaborative Spirit, Bold Ingenuity and Driving Excellence, through our twelve global competencies below, we help get more affordable medicines to more patients around the world. Fosters Teamwork Provides and Solicits Honest and Actionable Feedback Self-Awareness Acts Inclusively Demonstrates Initiative Entrepreneurial Mindset Continuous Learning Embraces Change Results-Oriented Analytical Thinking/Data Analysis Financial Excellence Communicates with Clarity We are proud to be an equal opportunity employer and we value diversity. BeiGene does not discriminate on the basis of race, religion, color, sex, gender identity, sexual orientation, age, disability, national origin, veteran status or any other basis covered by appropriate law. All employment is decided on the basis of qualifications, merit, and business need. BeiGene is a global, commercial-stage, research-based biotechnology company focused on molecularly targeted and immuno-oncology cancer therapeutics. Currently employees are located in APAC, Americas, and Europe. BeiGene is advancing a pipeline consisting of novel oral small molecules and monoclonal antibodies for the treatment of cancer. BeiGene is working to create combination solutions aimed at having both a meaningful and lasting impact on cancer patients. For more information, see www.beigene.com. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. At BeiGene, how we work is just as important as the work we do. Below are our Values that determine the decisions we make and how we do things. Patients First Bold Ingenuity Collaborative Spirit Driving ExcellenceÜber das Unternehmen:BeiGene Switzerland GmbH

Anforderungen: Proven finance capabilities (IFRS and Swiss or German statutory) and technical skills, solid understanding of finance processes and systems Financial degree or equivalent degree Collaboration and influencing skills Ability to work independently as well as part of a team Entrepreneurial spirit and curiosity that is inspirational to others Ability to navigate through complex, broad and diverse challenges Deliver compliant high quality financials, ensure company compliance Ability to work E2E with an enterprise view Passionate about transformation and catalyzing those changes across the network Commit to support your team’s development and growth, both as individuals and as a team Sprachen: Deutsch C1 Englisch C1 Referenznr.: 923162OKRolle: CAP MemberBranche: PharmaEinsatzort: BaselArbeitspensum: 100% (bis 2 Tagen pro Woche remote innerhalb der Schweiz)Start: 15.02.2024Ende: 15.08.2024 (mit Verlängerungsmöglichkeit)Sollte diese Position Ihr Interesse geweckt haben, senden Sie uns bitte Ihr komplettes Dossier via den Link in dieser Anzeige. Falls diese Position nicht so gut zu Ihrem Profil passt und Sie sich wünschen, andere Position direkt zu erhalten, können Sie uns Ihr Dossier ebenso via diese Anzeige oder an jobs[at]itcag[dot]com zukommen lassen.Kontaktieren Sie uns für weitere Informationen über unser Unternehmen, unsere Positionen oder unser attraktives Payroll-Only-Programm: +41 41 760 77 01.Über uns:ITech Consult ist ein nach ISO 9001:2015 zertifiziertes Schweizer Unternehmen mit Niederlassungen in Deutschland und Irland. ITech Consult ist spezialisiert auf die Vermittlung von IT-Kandidaten für Auftragsarbeiten. Wir wurden 1997 von IT-Profis gegründet und wissen daher, wie wichtig die professionelle Unterstützung bei der Projektsuche und -arbeit ist.ContractCAP MemberCAP Member (m/f/d) – IFRS/analytics/SOP/English/GermanProjekt / Rolle: For our Pharmaceuticals client in Basel we are looking for CAP Member who would bring strong finance expertise, together with the ability to work in a self-aligning team with minimal hierarchy. Sharing and receiving feedback, and living the collaborative accountability. They would be a catalyst for the Finance transformation and work effectively as an influencer, and leaning in as coach and catalyst to the Finance network as needed. They have a passion to comprehend new tasks and challenges, pilot new approaches and constructively challenge the status quo. They have a degree in Finance and have several years of experience in different finance areas.Hauptaufgaben:Variable accounting tasks based on the individual team needs Assist the preparation of the monthly Reporting for individual client Companies Prepare individual analytic reports Create new or maintain existing SOPs Controlling tasks Support individual Accounting Projects on request

AufgabenDurchführen von Daten-Analysen und Optimierungen, z.B. in den Bereichen Sales-based Ordering, Promotion, datengestützte Sortiment-Gestaltung, Logistik, interne ProzesseDatenextraktion aus verschiedenen Quellen, sowie anschliessende Data Preparation und -CleaningAuswertung/Interpretation und grafische Darstellung der AnalysenPräsentation der Ergebnisse und Diskussion der Anforderungen in verschiedenen Gremien, gemeinsame Ausarbeitung von Massnahmen inkl. ControllingLeitung von AI- und Data Science ProjektenExplorative Analyse von Daten und proaktive Suche nach neuen Use Cases für Prozessoptimierung mit Hilfe von Analytics und Artificial IntelligenceReviews von Algorithmen und statistischen ModellenMitarbeit in Projekten und/oder agilen ProduktteamsAnforderungenAbgeschlossenes Universitätsstudium (idealerweise Master) mit stark quantitativer Ausrichtung (z.B. Statistik, Mathematik, Physik, o.ä.)Fundiertes Know-how in Statistik: lineare und logistische Regression, Hypothesentests, Verteilungen, zusätzlich Kenntnisse von Algorithmen wie z.B. Random Forrest sind ein PlusKenntnisse der AI-Tool-Landschaft (z.B. GPT, Dall-E, Palm,...)Know-how in Programmierung von Python und/oder RAusgeprägte Kommunikationsfähigkeiten mit technischen und fachlichen StakeholdernBereitschaft nach der Einarbeitungsphase Projekte eigenständig zu koordinieren und Verantwortung für das analytische Endprodukt und die Prozesseinbindung zu übernehmen.Anwenderkenntnisse in SQL, MS Excel und PowerPoint von VorteilGenerell eine hohe Bereitschaft sich in neue Tools und Methoden einzuarbeitenNeugier und Interesse an betriebswirtschaftlichen Fragestellungen und Geschäftsprozessen, sowie Informatik-ThemenSehr gute Deutsch- und EnglischkenntnisseWas wir bietenattraktiv und sozialoffene und innovative Unternehmenskulturgrosszügige Rabatte in verschiedenen Coop-Formaten350 interne Kursetolle Freizeit- und Ferienangebote-COOPBaselAdresseCOOP24.01.2024 80% - 100% Data Scientist / Data Analyst und AI-Project Manager (m/w/d), 80 -100%

StellenbeschreibungGleichen Sie hier die Stellenbeschreibung mit Ihren Job-Präferenzen ab. Sie können die Job-Präferenzen jederzeit in Ihrem Profil verwalten.Anstellungsart100%Arbeitsort4052 Basel, BSEingebettet in das Data & AI Team von Accenture, bündelt Modern Data Platforms die Expertise in der ganzheitlichen Entwicklung und Umsetzung von innovativen Datenplattformen mit der Unterstützung von Automatisierungstechnologien. Von dieser geballten Power profitieren heute Unternehmen weltweit, um ihre Daten effizient zu nutzen und wertvolle Erkenntnisse zu gewinnen – und davon profitierst auch du! Denn wenn du unsere Begeisterung für die Entwicklung von modernen Datenplattformen und für hochautomatisierte Datenverarbeitung teilst, kannst du dein Talent und Können in vielfältigen Kundenprojekten unter Beweis stellen. Überall erwarten dich Top-Perspektiven und die fähigsten Köpfe der IT-Szene. Gehörst du bald dazu?Das erwartet dichDu förderst und entwickelst unsere Kunden auf dem Weg der digitalen Transformation mit deiner Persönlichkeit sowie deinem Können, Wollen und Wissen. Du ermöglichst eine aktive und engagierte Mitarbeit in einem dynamischen Team, nimmst Menschen mit auf die Reise, förderst die Zusammenarbeit und schaffst Transparenz. Dich erwartet nicht nur unsere Vision, IT-Lösungen zu entwickeln, die es noch nicht gibt, sondern auch ein lernendes Unternehmen in Transformation sowie ein kollegiales Umfeld mit einem engagierten und motivierten Team. Du übernimmst selbständig Verantwortung für den gesamten Projektumfang inklusive Steuerung des Budgets. Darauf freuen wir unsDu bringst fundierte Erfahrung als Projektleiter oder SCRUM Master in einem Dienstleistungsunternehmen mit und kennst dich in agilen Welten aus. Du hast das Projekt stets im Griff (Budget, Risiken und Lösungen), hast Spass an der Zusammenarbeit mit unterschiedlichen Stakeholdern sowie in unterschiedlichen Netzwerken und bist kreativ in der passenden Lösungsfindung. Du bist eine kommunikative, zielorientierte und umsetzungsstarke Persönlichkeit mit Überzeugungskraft, Durchsetzungsstärke und Verantwortungsbewusstsein. Ein breites Verständnis der technologischen Möglichkeiten im Bereich Datenplattformen und kennst die aktuellen Trends und Herausforderungen ist ein Plus. Du sprichst fliessend Deutsch und Englisch. Was wir dir bietenflexible Arbeitszeitmodelle, mobiles Arbeiten und die Option, in Teilzeit und/oder im Homeoffice zu arbeiten umfassende Trainingsangebote, Fort- und Weiterbildungsmöglichkeiten interessante Karriereoptionen unsere Arbeitskultur, die Diversität & Inklusion fördert den Zugriff auf den Wissens- und Erfahrungsschatz im globalen Accenture-Netzwerk Du und AccentureIn dieser Rolle bist du Teil von Accenture Technology. Wir nutzen das gesamte Spektrum digitaler Technologien, um den Alltag unserer Kunden zu vereinfachen. Und ihr Business in die Zukunft zu führen. Von #DevOps bis #Infrastruktur, von #Security bis #Workplace-Service.Die Accenture-Kultur: Hier machst DU den UnterschiedDeine Fähigkeiten, dein Naturell und deine Ambitionen machen dich einzigartig. Und wenn die unterschiedlichsten Talente, Stärken und Sichtweisen aufeinandertreffen, entsteht etwas Grossartiges: Ideen, die in der Welt etwas bewegen. Deshalb setzen wir bei Accenture auf Diversität und freie Entfaltung. Schaffe dir ein Arbeitsumfeld, in dem du aufgehst. Mit Aufgaben, die dir am Herzen liegen. Mit einem Workload, der zu dir passt. Und mit einer Arbeitsweise, die sich an deinen Zielen orientiert. Wie du dich vernetzen, weiterbilden und persönlich wachsen willst, liegt bei dir. Es ist deine Karriere. Wir helfen dir, sie so zu gestalten, wie du es dir vorstellst.Dein KontaktDu hast Fragen? Dann wende dich an unser Recruiting Team per E-Mail an [email protected] oder telefonisch unter 00 800 450 450 45.Wir freuen uns auf dich!#CIE #Data & AIErstellen Sie ein Indeed-Konto, bevor Sie zur Website des Unternehmens weitergeleitet werden.

AufgabenDurchführen von Daten-Analysen und Optimierungen, z.B. in den Bereichen Sales-based Ordering, Promotion, datengestützte Sortiment-Gestaltung, Logistik, interne Prozesse Datenextraktion aus verschiedenen Quellen, sowie anschliessende Data Preparation und -Cleaning Auswertung/Interpretation und grafische Darstellung der Analysen Präsentation der Ergebnisse und Diskussion der Anforderungen in verschiedenen Gremien, gemeinsame Ausarbeitung von Massnahmen inkl. Controlling Leitung von AI- und Data Science Projekten Explorative Analyse von Daten und proaktive Suche nach neuen Use Cases für Prozessoptimierung mit Hilfe von Analytics und Artificial Intelligence Reviews von Algorithmen und statistischen Modellen Mitarbeit in Projekten und/oder agilen Produktteams AnforderungenAbgeschlossenes Universitätsstudium (idealerweise Master) mit stark quantitativer Ausrichtung (z.B. Statistik, Mathematik, Physik, o.ä.) Fundiertes Know-how in Statistik: lineare und logistische Regression, Hypothesentests, Verteilungen, zusätzlich Kenntnisse von Algorithmen wie z.B. Random Forrest sind ein Plus Kenntnisse der AI-Tool-Landschaft (z.B. GPT, Dall-E, Palm,...) Know-how in Programmierung von Python und/oder R Ausgeprägte Kommunikationsfähigkeiten mit technischen und fachlichen Stakeholdern Bereitschaft nach der Einarbeitungsphase Projekte eigenständig zu koordinieren und Verantwortung für das analytische Endprodukt und die Prozesseinbindung zu übernehmen. Anwenderkenntnisse in SQL, MS Excel und PowerPoint von Vorteil Generell eine hohe Bereitschaft sich in neue Tools und Methoden einzuarbeiten Neugier und Interesse an betriebswirtschaftlichen Fragestellungen und Geschäftsprozessen, sowie Informatik-Themen Sehr gute Deutsch- und Englischkenntnisse Was wir bietenattraktiv und sozial offene und innovative Unternehmenskultur grosszügige Rabatte in verschiedenen Coop-Formaten 350 interne Kurse tolle Freizeit- und Ferienangebote KontaktAnne Marchon, HR MarketingMöchtest du deine analytischen Kenntnisse im dynamischen Umfeld eines Retailers praktisch einsetzen? Liebst du mathematische Herausforderungen und willst du etwas mit den Ergebnissen deiner Analysen bewegen? Willst du eigene Algorithmen und Logiken entwickeln, um Prozesse zu optimieren und zum Beispiel Food-Waste zu reduzieren?Das junge und dynamische Team "AI/ML Analytics" ist in der Coop Informatik angesiedelt und bearbeitet als zentrales Kompetenzzentrum analytische und mathematische Fragestellungen für die verschiedenen Abteilungen der Coop Gruppe.Data Scientist/Analyst wirst du Teil dieses interdisziplinären Teams und arbeitest vom ersten Tag an aktiv an verschiedenen Projekten und Analysen mit. Die Tätigkeitsschwerpunkte stellen ein ausgewogenes Verhältnis zwischen Teamwork und Einzelarbeit, zwischen Programmieren, Analysieren, Kommunizieren und Projektleitung dar. Zur Unterstützung stehen dir mehrere erfahrene Data Scientists, sowie der Teamleiter als Sparringpartner zur Seite.Coop Genossenschaft Vakant seit : 25.01.2024 4000 BASEL (BS) 80% - 100% Nach Vereinbarung Unbefristet Data Scientist / Data Analyst und AI-Project Manager (m/w/d), 80 -100%

Jobs suchenAnzeige schaltenLebenslauf einstellenAnmeldenData Scientist / Data Analyst und AI‐Project Manager ﴾m/w/d﴿, 80‐100%CoopBaselUnbefristetVollzeit17 Stunden herData Scientist / Data Analyst und AI‐Project Manager ﴾m/w/d﴿, 80‐100% CoopBewerben Lassen Sie sich diesen Job per E‐Mail zusendenSpeichernTeilenDiese Firma folgen