Gehaltsübersicht für Clinical Project Manager in Schweiz
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Gehaltsübersicht für Clinical Project Manager in Schweiz
96 667 ₣ Durchschnittliches Monatsgehalt
Durchschnittliches Gehaltsniveau in den letzten 12 Monaten: "Clinical Project Manager in Schweiz"
Das Balkendiagramm zeigt die Änderung des Gehaltsniveaus in der Clinical Project Manager Branche in Schweiz
Verteilung des Stellenangebots "Clinical Project Manager" in Schweiz
Wie die Grafik zeigt, in Schweiz gilt Kanton Neuenburg als die Region mit der größten Zahl der offenen Stellen in und an zweiter Stelle folgt Basel-Stadt. Den dritten Platz nimmt Kanton Genf ein.
Ranking der ähnlichen Stellenangebote gemäß dem Gehaltsniveau in Schweiz
Unter den ähnlichen Berufen in Schweiz gilt Group Credit Manager als der bestbezahlte Beruf. Laut unserer Webseite beträgt das Durchschnittseinkommen 140000 CHF. An zweiter Stelle folgt Controlling Manager mit dem Gehalt von 130000 CHF und den dritten Platz nimmt Senior Sales Manager mit dem Gehalt von 130000 CHF ein.
Project Manager - Digital Workplace
ONE Agency GmbH, Bern
Project Manager - Digital WorkplaceÜber unseren KundenUnser Kunde optimiert Geschäftsprozesse und sorgt dafür, dass die Produktivität verbessert wird. Ihr AufgabenbereichDas Führen eines motivierten Projekt-Teams, welches Kunden von der Analyse bis zur erfolgreichen Einführung begleitet.Die Herausforderung mittels intelligenter Lösungen Kunden glücklich zu machen.Spannende SharePoint und Office 365 Projekte mit führenden nationalen und internationalen Unternehmen aus aus den Branchen FSI, Public Sector und Energy.Die Projektverantwortung in Bezug auf Qualität, Zeit und Budget.Die Vorbereitung und Leitung von Kundenworkshops.Die Aufnahme fachlicher Anforderungen sowie die Beratung unserer Kunden rund um die Themen Digital Workplace, Collaboration, Intranet und DMS.Die Unterstützung im Presales bei der Gewinnung von spannenden Neukunden.Einsatz der neusten Technologien im Microsoft Umfeld.Ein begeistertes und innovatives Team mit grossem Erfahrungsschatz in der Umsetzung von SharePoint und Office 365 Projekten.Ihr ProfilEin abgeschlossenes Hochschulstudium in Informatik, Wirtschaftsinformatik oder Betriebswirtschaftslehre.Mehrjährige Erfahrung als Project Manager, Consultant oder Scrum Master im Web- / Software-Umfeld.Ein grosses Interesse an den Microsoft Plattformen, insbesondere SharePoint und Office 365 – Projekterfahrung in diesen Bereichen ist ein Plus.Du bist ein Kommunikations-Profi, stellst den Kunden ins Zentrum deines Handelns und übersetzt seine Bedürfnisse in konkrete Anforderungen.Du liebst Excellence in Qualität, fehlerlose Arbeitsresultate und bist bereit, gemeinsam mit dem Team die Extrameile zu gehen.Du bringst kreative Ideen mit und arbeitest mit unserem Kunden an der Vision der Collaboration Lösung der Zukunft.Du sprichst ausgezeichnetes Deutsch und kannst dich gut bis sehr gut auf Englisch verständigen.Ein Pensum von 80% bis 100% und flexible Reisebereitschaft in der deutschsprachigen Schweiz.Ihre ChanceBewirb dich jetzt!Ort:Bern Spezialisierung: Scrum (Methode) Scrum Master Project Manager/Requirement Engineering/Business Analysis Sharepoint Sprachen: Deutsch Englisch Job ID: 1850 |
Project Manager (f/m/d) Executive Office
Simens, Muenchen, Germany; Zug, Switzerland
What if you could find a role where you can truly impact Siemens' future? Do you thrive outside of your comfort zone? The Executive Office plays a vital role in writing the next chapter for our company. We're right at the center of the action, directly collaborating with a Siemens Managing Board Member business units CEOs and key functions, including strategy. Exposure to interesting projects and fascinating people is part of the job and a massive benefit for your development. The Executive Office acts as an accelerator for talent careers at Siemens. The Challenge? Join us and become a key player in our team! Work directly with the Managing Board Member responsible for Siemens Smart Infrastructure enabling the energy transition and creating sustainable communitiesYour tasks will span from leading high-profile projects to hands-on, content-driven support You will be part of strategic decisions and will regularly prepare Managing Board Meetings You will work in a fast-paced and interdisciplinary environment This will give you an outstanding opportunity to grow and build up a network at Siemens You’ll work in a diverse team that loves challenging the status-quoYour personal base should preferably be in Munich You!The basis for your success is an excellent academic track record You have at least 3 years of experience in management consulting (top-tier) or strategyYou know how to lead complex strategic and cross-functional projectsYou have solid experience in communicating, aligning, and managing stakeholders across multiple levels, including executive leadershipYou are a self-starter with strong analytical and interpersonal skillsYou feel comfortable in multi-national environments and off the beaten track. You see problems as opportunities, have a growth mindset, challenge the status quo and permanently strive for outstanding resultsYou are fluent in English and GermanMake your mark in our exciting world at Siemens.www.siemens.com/careers - if you would like to find out more about jobs & careers at Siemens.FAQ - if you need further information on the application process.As an equal-opportunity employer we are happy to consider applications from individuals with disabilities.Organization: Smart InfrastructureCompany: Siemens AGExperience Level: Experienced ProfessionalJob Type: Full-time
Project Manager - Space Planning and Design
Michael Page, Zürich
Follow-up and ensure the performance of missions, by complying with the deadlines and the undertakings, the security / health of the involved persons and the law ;Ensure the realisation of work and more generally the quality of services and the satisfaction of clients ;Draft all internal documents (Company and subcontractors) and external documents (clients) which allow the understanding and the follow-up of the project ;Participate to active phases of transfer ;Attend all meetings set by the management and the clients ;Realise technical and financial offers with the clients ;Referring subcontractors approved by the management.Experience of at least 5 years in such a global project manager role,Experience in retail architecture, workspace design and planning management, retail and hospitality projects, etc. is a plus,Fluent in German and English - mandatory,Any knowledge of French is a plus,Architecture or Engineer diploma is a plus (BA or Masters Degree),Both willing to work autonomously and in close collaboration with the team.
Project Manager - Electronic - EMS
, Lugano, Ticino
Tasks:Project management in compliance with the company objectivesManagement of the product lifecycleManagement of product portfolio: offers, orders, problems, changes, after sales, non conformitiesResponsible for the costs of the assigned productsContact with internal and external clientsPoint of contact for internal department involvedProfile:Technical education - electronic or electric fieldExperience in Project ManagementGood knowledge of English and GermanExcellent knowledge of MS Office (Excel is a must)Problem solving attitude and customer orientedGoal orientedAbility to find solutions and to give a strong service for internal and external clientsGood communication skills and pleasure to be part of a teamOrganization and precision skillsVostro contattoInteressato? Se le sue qualifiche ed esperienze corrispondono al profilo cercato, la preghiamo di candidarsi direttamente online.Il numero di referenza e 050-SITO-167382-10-IT.
Project Manager Business Development Operations
LGT Bank AG, Pfäffikon, Zürich, CH
LGT Capital Partners is a leading alternative investment specialist with USD 80 billion in assets under management and more than 600 institutional clients in 41 countries. An international team of over 600 professionals is responsible for managing a wide range of investment programs focusing on private markets, liquid alternatives and multi-asset class solutions. Headquartered in Pfaeffikon (SZ), Switzerland, the firm has offices in New York, Dublin, Frankfurt, London, Paris, Vaduz, Dubai, Beijing, Hong Kong, Tokyo and Sydney.Project Manager Business Development OperationsStellenbeschreibungThe Business Development (BUD) team is looking for an Operations Specialist to support with the enhancement of its systems and processes. New systems need to be implemented and processes within BUD need to be improved and standardized. Data and documents need to be made readily available anytime and in all 10 offices with the Firmu2019s sales representatives.Job informationEnsuring a smooth operation of the entire BUD platform, including dedicated business processes;Support the design and implementation off new systems, such as DealCloud CRM, a Management Information System and task management systems;Collaborating with BUD staff globally, including Relationship Managers and ensuring the efficiency of their daily work;Supporting BUD management in all operational elements;Improving availability of data & documents for both clients as well as internal stakeholders;Controlling regulatory processes and ensuring adherence by RMs.Unsere AnforderungenBachelor degree in business administration, marketing, economics or similar;At least 2 yearsu2019 relevant work experience in a similar role;Efficient project management, conceptual and execution skills;Solid understanding of business processes, CRM systems and regulatory frameworks;Experience in the asset management or financial industry in an international environment is a plus;Strong analytical thinking paired with excellent communication skills both in English and German;Team player with distinct organizational skills and attention to detail;Customer-oriented, open-minded, motivated and flexible personality with a high level of initiative.KontaktinformationenIf you are interested in becoming an integral part of a successful alternative investment management team in an international, multicultural working environment we will be pleased to get to know you soon.For further information please contact us.Cassandra FritschiLGT Capital Partners AG, PfaeffikonHuman Resources
Clinical Trial Manager (Homebased - Europe) - Iqvia Biotech
IQVIA Biotech is a unique division specialising in working with smaller biotech and emerging biopharma clients and as such we have a vibrant, fast-paced working environment. The sector we are in is cutting edge for therapies with un-met medical need. Clinical Trial Managers at IQVIA Biotech are responsible for the planning, implementation and execution of contracted clinical monitoring activities. They are functionally responsible for all clinical monitoring team members throughout the duration of each clinical trial. Responsibilities of this role include: Working closely with the Project Manager to define programme targets for clinical monitoring staff and ensure work is do
Senior Clinical Project Manager
AC Immune SA, Lausanne
Function Senior Clinical Project Manager (Senior CPM) Percentage 100 % Reporting Line Group Leader Clinical Operations (GLCO) Company Profile • AC Immune is a clinical stage Swiss biotech company focused on the development of innovative therapeutics and diagnostics for Alzheimer’s and other neurodegenerative diseases • 140 Employees, 20 nationalities, IPO in 2016, listed on NASDAQ • AC Immune SA is a progressive, equal opportunity employer Job description The Senior Clinical Project Manager is responsible, under the supervision of the GLCO, of the management of international and/or complex studies according to time, cost and quality standards. Key Responsibilities • Manage international and/or complex clinical studies according to time, cost and quality standards • Negotiate, implement and maintain contracts with study partners (study vendors, sites) • Manage activities of study partners, support clinical CRO in managing the sites • Review and approve submission packages for submission to Ethics Committees/Institutional Review Boards • Supply proper documentation to the regulatory department for submission to Regulatory Authorities • Contribute to the generation of SOPs/WIs and share experience and expertise when reviewing documents created by other members of the clinical team • Participate in clinical study design • Create and maintain operational plans • Prepare study budgeting and forecasting • Global budget management of studies • Ensure the accurate planning and ordering of clinical study drug supply • Write and update clinical study documents • Participate to review and approval of the Clinical Trial Report • Be responsible for the Trial Master File • Participate in study specific core team meetings • Serve as a mentor and as a dedicated point of contact for operational related questions for junior team members within the clinical team Qualifications & Skills Required: • Minimum of 6 years of experience in clinical research (with 4 years coordinating international or leading regional studies) • Previous monitoring experience and knowledge in international standards (GCP/ICH) as well as in international (FDA/EMA) and local regulations • Hands on experience in writing clinical study documents • A scientific degree is required as well as the ability to work in a start-up environment, handling multiple demands and strong planning and organizational skills o Advanced understanding of timelines, budget and resource management o Planning, tracking and solving skills for maintaining project timelines Senior Clinical Project Manager o Working both independently and in a cross-functional team setting o Good spoken and written English are required
Clinical Project Manager early phases
Axepta SA, Lausanne
My client is an innovating, dynamic and niche international biopharma company based in Switzerland currently expanding their activities and projects.Due to this growth my client is looking for a Senior International Clinical Project Manager with strong experience at a global level on complex phase I and II global trials.The position is a 12 month contract (minimum) Lead the overall initiation, coordination, implementation and management of large international clinical trials from start-up to close out. Lead the cross functional study team dedicated to the clinical study to ensure clinical program goals and timelines are met; Manage operational and technical aspects of projects including budgeting, study initiation and risk management; Anticipate potential issues and risks within the clinical program, create contingency plans and drive solution implementation; Assist in the identification of investigational sites and coordinate co-monitoring with CRAs when required; Represent clinical operations on multi-function project teams internally and externally; report on study progress; Establish study milestones and ensure accurate tracking and reporting of study metrics and timelines, alert in case of deviations or risks, and propose mitigation plans; Provide operational input (and scientific if appropriate) into Protocol synopsis, Study protocol and all other study related documents; Select, manage and coordinate external vendors, such as Contract Research Organizations (CROs), central laboratories, etc Monitor vendor and CROs performance and ensure continuous oversight; Design, review and approve of all trial related documentation, and establish trial processes. Your Profile : University degree or equivalent in Life Sciences. Fluent in English – French is an asset Proven track record of successful management of large complex clinical trials in the Pharmaceutical Industry or CRO. Deep knowledge and experience on the implementation and use of EDC, IWRS, eTMF, CTMS and any other digital clinical trial systems. Experience in management of CROs, vendors and consultants. Excellent budgeting, planning, and communication skills. Ability to lead and influence a cross-functional study team and external partners. Team Leader & Recruitment Management Life Sciences Life Sciences Recruitment Specialist Marine DOLLAT Life Sciences Recruitment Specialist Apply For This AD Maximum file size: 300 MB. Allowed Type(s): .pdf, .doc, .docx Maximum file size: 300 MB. Allowed Type(s): .pdf, .doc, .docx By using this form you agree with the storage and handling of your data by this website. To revoke my consent or obtain more information, we invite you to contact Axepta SA directly.
Clinical Project Manager
Axepta SA, Genf
We are looking for a Clinical Project Manager , for one of our prestigious, world-renowned and fast-growing clients specialized in Medical Devices, located in Geneva. Be part of the young and dynamic Clinical Research Department for the implementation of clinical studies to ensure compliance with new MDR regulatory updates. Implement and conduct clinical research operations in clinical studies Conduct clinical studies in accordance with local regulations, GCP regulations and internal standard operating procedures Select and validate investigator/site and vendors (CRO). Actively contribute to the negotiation and preparation of contracts and budgets with third parties and study sites Manage CROs and ensure work and studies are completed on time and on budget Write and maintain clinical and quality documentation throughout the clinical study (from study protocol to clinical study report) Manage clinical study budgets, including site agreements/budget Conduct co-monitoring visits to ensure monitor performance meets expectations Your Profile : You have a B.Sc. degree in relevant scientific discipline e.g. Biochemistry, Microbiology, Pharmacy, Biological Sciences or Related Pharmaceutical Science A minimum of 4 years’ experience in Clinical Operations and project management (late phase studies is a plus) Fluent in English required / French is a plus For more details, apply here or contact Morgane CAYUELA at: mcaxepta.com Life Sciences Recruitment Specialist Team Leader & Recruitment Management Life Sciences Marine DOLLAT Life Sciences Recruitment Specialist Apply For This AD Maximum file size: 300 MB. Allowed Type(s): .pdf, .doc, .docx Maximum file size: 300 MB. Allowed Type(s): .pdf, .doc, .docx By using this form you agree with the storage and handling of your data by this website. To revoke my consent or obtain more information, we invite you to contact Axepta SA directly.
SR. CLINICAL PROJECT MANAGER
gloor & lang ag life science careers, Baden
Late Stage Clinical Development Novel Indications SR. CLINICAL PROJECT MANAGER Interested in supporting an innovative company in Basel through the exciting journey of late stage clinical trials? The development of promising products for novel therapeutic indications will be continued in 2022. Bring your experience, your energy, and in-depth specialist knowledge into the small dynamic team. As a Sr. Project Manager, you will be responsible for the operational implementation and management of the assigned clinical study(ies). All tasks related to study plan, time management of the studies, required trial drugs and budget control are within your scope of responsibility. You draft and update project management plans and monitor, control, and coordinate the studies carried out. Your challenges: Operational conduct and management of assigned clinical trial(s) Development of clinical study protocols and related documents Selection and qualification of trial sites and investigators Selection and evaluation of CROs Management and oversight of CROs from set-up to project completion Contribution to the development of regulatory documents (e.g., IB / IMPD / DSUR) and responses to Health Authorities/Ethics Your profile: University degree in life sciences / health care or equivalent Minimum of 6 years experience in managing clinical trials in pharma or CRO Open, team-oriented, and communicative personality Sound knowledge of ICH-GCP requirements Fluent in English and ideally in one further language, preferably German As a hands-on person, you have the ability to independently manage projects. An open and informal exchange with all involved stakeholders is a key factor in your success. Your accurate and precise work approach, together with initiative and focus on the next milestones are essential skills you will build on in your daily work. A particularly responsible role in a dynamic company with highly promising products. Interested? We are looking forward to get in touch with you.