3 Artificial Intelligence jobs

Writing the future. Together. Avaloq is a value-driven fast-paced fintech company and we are committed to develop the banking technology of tomorrow. Leading banks and wealth managers in all major financial centres rely on our software and services, and this unique community grows every day. Your team Asset Master Data team cover mainly the following: Asset Opening and modification Classes and component enrichment Price management Business partner administration There is interaction with the clients for new projects and requests, as well as with all the other internal teams Your mission Update and enhance the financial instruments Masterfile and the counterparties Masterfile of our bank clients Manage prices for client’s financial instruments sets, interacting with data providers where required Execute inquiries on counterparties or financial instruments to different entities (data providers, client banks, other units in the company) What you need Banking/financial educational background Work experience in the Asset Master Data back office field is considered as a strong advantage Excellent knowledge of Microsoft Office products, in particular MS Excel Knowledge of Avaloq, SIX FI ID and Bloomberg are an asset Proven service and client orientation Very good communication skills Strong motivation to be part of a dynamic team and acquire new competences in the Asset Master Data field Fluent in English. German, French and Italian are considered a plus Now let’s talk about perks and compensation With our compensation model, we want to share the success of the company with all our employees. We offer competitive base salaries and if you prove yourself as a super-star, you might be entitled to an extraordinary achievement reward. Place of work Bioggio Part-time position: 50% Working days per week: 5 Don’t be shy – apply! Contact Recruiter: Avaloq Evolution AG Anna Drozdowska careers@avaloq.com www.avaloq.com/en/open-positions Please only apply online. Note to Agencies: All unsolicited résumés will be considered direct applicants and no referral fee will be acknowledged.

Req #:   1903685 Location:   Boudry, Neuchatel, Switzerland Job Category:   Medical Work Location:   Route de Perreux 1 2017 Organization:   Clinical Research Scientist Employee Status:   Full-time Job Type:   Temporary Here at Celgene, we are seeking an experienced and self-sufficient Clinical professional to play a pivotal role in the progress of our CAR T clinical work, and to join our team as Clinical Research Scientist. As we seek to push the boundaries of medical innovation, we are seeking an individual who is knowledgeable / well-versed in verifying and reviewing clinical data - you will, therefore, have experience from either a Clinical Research Organisation (CRO) or a pharma/biotech setting, As a Clinical Research Scientist, you will play a key role within the Lymphoma Team. Working closely with the study team, you will support the clinical study activities as well as collaborate with clinical team members - you will also liaise closely with non-Clinical team members as to provide deliverables. Because of this, it is essential that you have experience from within Hematology or Oncology. In this role, you will be empowered to achieve your personal goals which support study team and project team goals - this will be aided by your colleagues, a diverse and experienced set of individuals who form the Global team. Please note: This is a 12-month temporary assignment, based out of our International HQ in Neuchatel, Switzerland. (due to acute business needs, preference will be given to those candidates who are already located in Switzerland and available at short notice) Responsibilities will include, but are not limited to, the following: Support assigned study level activities with a minimal level of supervision (may lead or co-lead a study or study activities) Thorough understanding of assigned protocol and protocol requirements Successfully plans execution of deliverables Support all study start-up/conduct/close-out activities as applicable Preparation, storage, maintenance of clinical documents (TMF) Coordination of protocols & amendments; may author with guidance Review and validation of clinical study reports (CSRs); demonstrate basic understanding the connection between the data and the CSR Conduct literature review as needed Provide study related information to support Regulatory Documents (e.g., IB, Briefing Books) Review Informed Consent Forms (ICF); may author a global or regional ICF template Preparation of site and CRA training materials; may present information Country/site selection activities as requested Collaboration with Clinical Operations for budget preparation, CRO scope, etc. (i.e., review and provide feedback on activities/instructions/deliverables related to study data, IVRS, central labs, patient reported outcomes) Support study committee (e.g., DMC) activities (e.g., charters, meetings, presentations) Support Investigator Meeting and SIV planning/facilitation, including slide preparation Review clinical data for specific trends, mine data to support responses to HA or EC questions as requested Clinical review of study data (conduct clinical data review, communicate as necessary to resolve data queries, draft/update/review data review plans, support Clinical Research Physician in data review (generation of reports, action plans, trend identification), etc) Collaborate with study team members including: Clinical Operations, Data Management, Statistics, Drug Safety, IMSC, Regulatory Affairs, Translational Medicine and Project Management (set-up and/or lead meetings as appropriate) Regularly attend and actively participate in study team and other clinical meetings. Seek out and enact best practices with minimal instruction; contribute to process improvement. Actively seek and receive coaching/mentoring; may provide guidance to junior members of team. Contribute to preparations for external/stakeholder meetings (e.g., IMs, Governance) May present data/information to external investigators or study staff (e.g., SIV presentations) Provide regular and timely updates to manager Identify & escalate current/future issues; may propose solutions Set own priorities with moderate guidance from manager. IN MANAGER's WORDS, the top 3 requirements are: 1. Clinical/Medical background and experience as a Clinical Research Scientist 2. Must have at least two years of direct HEMATOLOGY/ONCOLOGY experience in a Clinical Research and Development capacity 3. Must be able to function independently Skills/Knowledge Required : At least 4 years of experience in CR&D roles/responsibilities or equivalent Knowledge of GCP/ICH, overall drug development process from discovery to registration, study design, statistics, clinical operations Excellent verbal, written, communication and interpersonal skills Demonstrates initiative Detail-oriented Knowledge and skills to support program specific data review and trend identification Knowledge of Medical Terminology and basic medical writing skills Knowledge of the disease area(s), KOLs, indication(s), compound(s) under study (including MOA & safety profile) Knowledge of the establishment and operation of data monitoring committees, dose review teams, and independent response adjudication committees. Understanding of functional and cross-functional relationships Commitment to Quality Adaptable / Flexible (willing and able to adjust to multiple demands and shifting priorities; ability to meet day-to-day challenges with confidence and professionalism) Strong planning/project management skills (ability to develop short range plans that are realistic and effective in meeting goals) Proficient in Microsoft Word, Excel, PowerPoint, Electronic Data Capture (e.g., RAVE), J-Review or similar data reporting tools About Us COMMITTED TO IMPROVING THE LIVES OF PATIENTS WORLDWIDE At Celgene, we seek to deliver truly innovative and life-changing drugs for our patients. Our vision as a company is to build a major global biopharmaceutical corporation while focusing on the discovery, the development, and the commercialization of products for the treatment of cancer and other severe, immune, inflammatory conditions. "At Celgene, we seek to deliver truly innovative and life-changing drugs for our patients." There are more than 300 clinical trials at major medical centers using compounds from Celgene. Investigational compounds are being studied for patients with incurable hematological and solid tumor cancers, including multiple myeloma, myelodysplastic syndromes, chronic lymphocytic leukemia (CLL), non-Hodgkin’s lymphoma (NHL), triple-negative breast cancer and pancreatic cancer. As committed as we are to clinical accomplishment, we are equally committed to patient support, which is a guiding principle at Celgene. We believe all who can benefit from our discoveries should have the opportunity to do so. Celgene puts patients first with industry-leading programs that provide information, support and access to our innovative therapies.

Datenanalyse und Digitalisierung zugunsten der Gesellschaft Die Finanzstatistik publiziert die Daten der Finanzhaushalte des gesamten Staatssektors (Bund, Kantone, Gemeinden und öffentliche Sozialversicherungen) und ist Teil des statistischen Systems der Schweiz. Das neue Team "Digitalisierung" ist beauftragt, Kenntnisse der modernen Tools zur Datenbearbeitung und Analyse auszubauen und diese in der Finanzstatistik einzusetzen. Sie tragen damit zu einer effizienten Erfüllung der Aufgaben bei und optimieren damit die Prozesse der Finanzstatistik. Insbesondere helfen Sie mit, die steigenden Anforderungen der internationalen Organisationen (G20, IWF, Eurostat, usw.) umzusetzen. IHRE AUFGABEN Erstellung von empirischen Analysen und Prognosen anhand modernen quantitativen Methoden (Ökonometrie, Künstliche Intelligenz und Machine Learning) zu makroökonomischen, finanz- und steuerpolitischen relevanten Fragestellungen Betreuung, Erweiterung und Neuentwicklung der Fachanwendungen (in «R», «Python», usw.) Umsetzung der Digitalisierungsstrategie der EFV in der Finanzstatistik. Automatisierung und Optimierung der Prozesse der Datenproduktion Mitwirkung bei der Weiterentwicklung des statistischen Systems der Schweiz in Zusammenarbeit mit dem Bundesamt für Statistik (BFS) Bereitstellung von Hintergrundinformationen und Entscheidgrundlagen für die Departementsleitung sowie die Direktion IHRE KOMPETENZEN Master oder Doktorat in Datenwissenschaften, Ökonometrie, angewandte Statistik oder gleichwertige Ausbildung Analytisches und konzeptionelles Denkvermögen; Fähigkeit, die Ergebnisse der Arbeit klar und prägnant zu präsentieren; ausgeprägte Problemlösungskompetenzen Sehr gute aktive Programmierkenntnisse, die für die Datenanalyse relevant sind (R/Python/Java/SQL, usw.). Bei Bedarf, Bereitschaft weitere Programmiersprachen und quantitative Methoden zu lernen Wenn möglich Kenntnisse der volkswirtschaftlichen Gesamtrechnung und der internationalen statistischen Standards Teamfähigkeit, sehr gute Kenntnisse zweier Amtssprachen; Kenntnisse der dritten Amtssprache sind von Vorteil Zusatzinformationen Fachliche Auskünfte erteilt Ihnen gerne: Herr Florian Chatagny, Leiter Sektion Finanzstatistik, Tel. 058 467 87 91 Allfällige postalische Bewerbungen senden Sie bitte an: DLZ Pers EFD, Eigerstrasse 71, 3003 Bern Referenznummer: 601-39988