178 Jobs für Protocol Manager
Stellenangebote Protocol Manager Jobs
Job gestern bei StepStone gefunden
Protocol Hero GmbH
• Köln Koeln
Beratungs-/ Consultingtätigkeiten
Protocol Hero baut die Plattform, die Handwerksbetriebe von Papier, Chaos und Excel befreit. Unser Ziel ist klar: Dokumentation und Prüfprotokolle sollen so einfach werden, dass sie im Arbeitsalltag ganz selbstverständlich [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] nebenbei entstehen. Schnell, sauber, nachvollziehbar und bereit für Kunden, Abnahme, Versicherung und im Zweifel auch für den Streitfall. Dafür entwickeln wir [. .. ] unseren Vertrieb, um aktiv auf neue Handwerksbetriebe zuzugehen. Unser Produkt ist validiert, hunderte Betriebe nutzen es bereits. Deine Aufgabe ist es, den Erstkontakt herzustellen und qualifizierte Termine für unsere Sales Manager zu vereinbaren, mit der klaren Perspektive, den Prozess später selbstständig bis zum Abschluss zu führen. Outbound Terminvereinbarung Identifikation passender Betriebe und Ansprechpartner Aktive telefonische Ansprache potenzieller Kunden (Outbound Calling) Vereinbarung von Demo-Terminen Dokumentation der Gespräche und Pflege der Kontakte im CRM Unterstützung im Sales-Prozess Enge Zusammenarbeit mit dem [. .. ]
Job vor 2 Tagen bei StepStone gefunden
Protocol Hero GmbH
Werkstudent-Sales Development Representative/ Vertriebsmitarbeiter (m/w/d)
• Köln Koeln
Beratungs-/ Consultingtätigkeiten Teilzeit Werkstudenten
Protocol Hero baut die Plattform, die Handwerksbetriebe von Papier, Chaos und Excel befreit. Unser Ziel ist klar: Dokumentation und Prüfprotokolle sollen so einfach werden, dass sie im Arbeitsalltag ganz selbstverständlich [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] nebenbei entstehen. Schnell, sauber, nachvollziehbar und bereit für Kunden, Abnahme, Versicherung und im Zweifel auch für den Streitfall. Dafür entwickeln wir [. .. ] unseren Vertrieb, um aktiv auf neue Handwerksbetriebe zuzugehen. Unser Produkt ist validiert, hunderte Betriebe nutzen es bereits. Deine Aufgabe ist es, den Erstkontakt herzustellen und qualifizierte Termine für unsere Sales Manager zu vereinbaren, mit der klaren Perspektive, den Prozess später selbstständig bis zum Abschluss zu führen. Outbound Terminvereinbarung Identifikation passender Betriebe und Ansprechpartner Aktive telefonische Ansprache potenzieller Kunden (Outbound Calling) Vereinbarung von Demo-Terminen Dokumentation der Gespräche und Pflege der Kontakte im CRM Unterstützung im Sales-Prozess Enge Zusammenarbeit mit dem [. .. ]
Job gestern bei Jooble gefunden
Alimentiv
• Hamburg
Führungs-/ Leitungspositionen
[. .. ] clinical operations of a project within a defined regional/ global level. Provides oversight of project deliverables, assigned Clinical Research Associate (CRAs) and Investigator sites in accordance with [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] the Monitoring Plan, Protocol, Good Clinical Practice (GCP) , ICH guidelines and local regulations. The COL acts as a primary liaison between the CRAs and the clinical project team. Additional responsibilities include project specific training of CRAs, conducting assessment visits with CRAs, implementation of enrollment and recruitment strategies, preparation of the monitoring plan and [. .. ] for study-specific questions and issues. Escalates to PM and other functions as appropriate. Support line managers by providing status updates on utilization and performance of CRAs. Liaise with line manager for assigning sites to CRAs following line manager allocation of a CRA resource to the project. Conduct CRA Assessment visits per departmental requirements to assess the performance of the CRA against their monitoring responsibilities. Study Documents and Plans Develop training materials and study tools for sites and CRAs, including monitoring [. .. ]
Job vor 2 Tagen bei Jooble gefunden
Study Physician sponsor dedicated in Germany
• München
[. .. ] cardiology, pediatrics, emergency medicine are preferred) with following experience: Global Medical Monitor/ Study Physician/ Clinical Trial Physician managing phase I to IV clinical trials in CRO/ Pharma [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] company. Global Project Manager/ Clinical Trial leader/ Project manager managing multiple countries in CRO/ Pharma company. Country Trial Manager/ Local Project Manager/ Project Manager USA in CRO/ Pharma company Global Safety Physician/ Risk Management Physician in Pharmacovigilance department in CRO/ Pharma company Additional Points: Clinical practice experience of minimum 4 yrs is mandatory. Normally [. .. ] investigator/ sub investigator in clinical trials for a reasonable amount of time. Travel-15-20 depending on the study requirements. Key words to look for in potential CVs-Clinical Trial protocol-writing/ reviewing, Identify medically relevant critical data, Medical risks, risk mitigation/ monitoring plan, Medical quality review/clinical quality monitoring, Jreview, Able to use Spotfire, Medical data/ listings review, Medical plausibility check, Patient profile review, Trial documents review (Informed consent, Trial monitoring manual, Trial training plan etc) , Clinical trial report [. .. ]
Job vor 5 Tagen bei Jooble gefunden
• München
[. .. ] Responsibilities Performs site qualification, site initiation, interim monitoring, site management and close-out visits (performed on-site or remotely) ensuring regulatory, ICH-GCP and/or Good Pharmacoepidemiology Practices (GPP) and
protocol [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] compliance. Uses judgment and experience to evaluate overall performance of site and site staff and to provide recommendations regarding site-specific actions; immediately communicates/ escalates serious issues to the project team and develops action plans. Maintains a working knowledge of ICH/ GCP Guidelines or other applicable guidance, relevant regulations, and [. .. ] training and sign off visits for junior CRA staff, as assigned. May be mentored and assigned lead tasks under supervision of an experienced Clinical Operations Lead (COL) or operational line manager. This could include participation in business development proposals and/or defense meetings. Qualifications: Bachelors degree or RN in a related field or equivalent combination of education, training and experience Knowledge of Good Clinical Practice/ ICH Guidelines and other applicable regulatory requirements Preferably oncology experience Must demonstrate good computer skills and [. .. ]
Job vor 8 Tagen bei Jooble gefunden
Abb Vie
Clinical Study Specialist (Contract)
• Wiesbaden
Work-Life-Balance
[. .. ] Linked In and Tik Tok. Supports in the in-house organization, management and execution of projects to ensure the clinical trials are conducted, recorded, and reported in accordance [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] with the protocol, federal regulations and applicable local regulations, Good Clinical Practices (GCPs) , ICH Guidelines, Abb Vie Standard Operating Procedures (SOPs) , Monitoring Plans, and to quality standards in conducting clinical research. Participates in the study startup activities and site opening activities as well as study conduct and site closure tasks. Ensures [. .. ] experience. One year of clinically-related experience in a medical profession, pharmaceutical, or diagnostic company is preferred. Knowledge of conducting industry-sponsored clinical research (e. g. Clinical study coordinator/ data manager, clinical trial assistant (or equivalent) , regulatory document specialist) is preferred. Strong planning and organizational skills and the ability to work effectively and efficiently in a dynamic environment with competing projects and deadlines. with a diverse work environment where you can have a real impact with an attractive salary with [. .. ]
Job vor 8 Tagen bei Jooble gefunden
Abb Vie
• Wiesbaden
Work-Life-Balance
[. .. ] Linked In and Tik Tok. Supports in the in-house organization, management and execution of projects to ensure the clinical trials are conducted, recorded, and reported in accordance [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] with the protocol, federal regulations and applicable local regulations, Good Clinical Practices (GCPs) , ICH Guidelines, Abb Vie Standard Operating Procedures (SOPs) , Monitoring Plans, and to quality standards in conducting clinical research. Participates in the study startup activities and site opening activities as well as study conduct and site closure tasks. Ensures [. .. ] experience. One year of clinically-related experience in a medical profession, pharmaceutical, or diagnostic company is preferred. Knowledge of conducting industry-sponsored clinical research (e. g. Clinical study coordinator/ data manager, clinical trial assistant (or equivalent) , regulatory document specialist) is preferred. Strong planning and organizational skills and the ability to work effectively and efficiently in a dynamic environment with competing projects and deadlines. with a diverse work environment where you can have a real impact with an attractive salary with [. .. ]
Job vor 8 Tagen bei Jooble gefunden
Abb Vie
Contract Clinical Research Associate
• Wiesbaden
Work-Life-Balance
[. .. ] Linked In and Tik Tok. Supports in the in-house organization, management and execution of projects to ensure the clinical trials are conducted, recorded, and reported in accordance [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] with the protocol, federal regulations and applicable local regulations, Good Clinical Practices (GCPs) , ICH Guidelines, Abb Vie Standard Operating Procedures (SOPs) , Monitoring Plans, and to quality standards in conducting clinical research. Participates in the study startup activities and site opening activities as well as study conduct and site closure tasks. Ensures [. .. ] experience. One year of clinically-related experience in a medical profession, pharmaceutical, or diagnostic company is preferred. Knowledge of conducting industry-sponsored clinical research (e. g. Clinical study coordinator/ data manager, clinical trial assistant (or equivalent) , regulatory document specialist) is preferred. Strong planning and organizational skills and the ability to work effectively and efficiently in a dynamic environment with competing projects and deadlines. with a diverse work environment where you can have a real impact with an attractive salary with [. .. ]
Job vor 8 Tagen bei Jooble gefunden
Abb Vie
• Wiesbaden
Work-Life-Balance
[. .. ] Linked In and Tik Tok. Supports in the in-house organization, management and execution of projects to ensure the clinical trials are conducted, recorded, and reported in accordance [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] with the protocol, federal regulations and applicable local regulations, Good Clinical Practices (GCPs) , ICH Guidelines, Abb Vie Standard Operating Procedures (SOPs) , Monitoring Plans, and to quality standards in conducting clinical research. Participates in the study startup activities and site opening activities as well as study conduct and site closure tasks. Ensures [. .. ] experience. One year of clinically-related experience in a medical profession, pharmaceutical, or diagnostic company is preferred. Knowledge of conducting industry-sponsored clinical research (e. g. Clinical study coordinator/ data manager, clinical trial assistant (or equivalent) , regulatory document specialist) is preferred. Strong planning and organizational skills and the ability to work effectively and efficiently in a dynamic environment with competing projects and deadlines. with a diverse work environment where you can have a real impact with an attractive salary with [. .. ]
Job vor 8 Tagen bei Jooble gefunden
Abb Vie
Clinical Senior Research Associate
• Wiesbaden
Work-Life-Balance
[. .. ] Linked In and Tik Tok. Supports in the in-house organization, management and execution of projects to ensure the clinical trials are conducted, recorded, and reported in accordance [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] with the protocol, federal regulations and applicable local regulations, Good Clinical Practices (GCPs) , ICH Guidelines, Abb Vie Standard Operating Procedures (SOPs) , Monitoring Plans, and to quality standards in conducting clinical research. Participates in the study startup activities and site opening activities as well as study conduct and site closure tasks. Ensures [. .. ] experience. One year of clinically-related experience in a medical profession, pharmaceutical, or diagnostic company is preferred. Knowledge of conducting industry-sponsored clinical research (e. g. Clinical study coordinator/ data manager, clinical trial assistant (or equivalent) , regulatory document specialist) is preferred. Strong planning and organizational skills and the ability to work effectively and efficiently in a dynamic environment with competing projects and deadlines. with a diverse work environment where you can have a real impact with an attractive salary with [. .. ]
Job vor 9 Tagen bei Jooble gefunden
Abb Vie
• Wiesbaden
Work-Life-Balance
[. .. ] and Tik Tok. Job Description Supports in the in-house organization, management and execution of projects to ensure the clinical trials are conducted, recorded, and reported in accordance [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] with the protocol, federal regulations and applicable local regulations, Good Clinical Practices (GCPs) , ICH Guidelines, Abb Vie Standard Operating Procedures (SOPs) , Monitoring Plans, and to quality standards in conducting clinical research. Participates in the study startup activities and site opening activities as well as study conduct and site closure tasks. Manages [. .. ] and understanding of appropriate therapeutic indications as they relate to the conduct of clinical trials is preferred Knowledge of conducting industry-sponsored clinical research (e. g. Clinical study coordinator/ data manager, clinical trial assistant (or equivalent) , regulatory document specialist) is preferred. Knowledge related to ICH/ GCP Guidelines and applicable local regulations is preferred. Strong planning and organizational skills and the ability to work effectively and efficiently in a dynamic environment with competing projects and deadlines. Ability to work, understand and [. .. ]
Job am 20.01.2026 bei Jooble gefunden
CEF AI
Blockchain Engineer
• Berlin
[. .. ] hype. We are seeking a Lead Blockchain Engineer with strong experience in designing, developing, and operating Layer 1 (L1) blockchain systems. In this role, you will work [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] on the Cere protocol, which underpins CEFs decentralised data and compute architecture. You will be responsible for evolving the core protocol, maintaining production networks, and improving the surrounding ecosystem tooling, as part of our work on autonomous and sovereign data computing. Tasks Architect Core Protocol: Continuously upgrade the Cere Protocol L1 blockchain using Rust [. .. ] real collaboration. Heres what the process looks like: Intro Call A quick chat to align on expectations, interests, and team fit. Technical Deep Dive A focused conversation with our Engineering Manager to explore your technical thinking and past work. CEO Interview A strategic discussion around vision, mindset, and long-term alignment. Reference Collection Well speak with a few people youve worked closely with. Paid Trial (5 Days) A short, real-world engagement so we can see how we work together happening [. .. ]
Job am 18.01.2026 bei Jooble gefunden
Ventura TRAVEL
• Frankfurt am Main
[. .. ] them like friends and make sure their trip with us will be the best experience they can have. You keep calm even when it gets stressful, act [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] according to the protocol in special circumstances, and can help out with flexible solutions on your own. You are interested in sustainable, local authentic travel. We prefer that you have some experience, but also welcome the newly graduate too What we promise you Advance training and development program in areas such as languages, history [. .. ] co-workers. Confidentiality Diversity Applications at Ventura TRAVEL are treated with strict confidentiality. We use a professional HR-Software that only grants access to your applications to HR, the Recruiting Manager, and the interviewers. It is our commitment that every qualified person will be evaluated according to skills regardless of age, gender identity, ethnicity, sexual orientation, disability status, or religion. 76732982 [. .. ]
Job am 17.01.2026 bei Jooble gefunden
BAUHAUS
Manager Nachhaltigkeit (m/w/d)
• Mannheim
Flexible Arbeitszeiten Betriebliche Altersvorsorge 30+ Urlaubstage Work-Life-Balance
[. .. ] Kennzahlen und die Umsetzung von Nachhaltigkeitsmaßnahmen. Den Nachhaltigkeitsbericht erstellen Sie konform zu regulatorischen Anforderungen (CSRD, ESRS, EU-Taxonomie) . Jährlich erheben und berechnen Sie die CO2-Bilanz nach dem [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] GHG Protocol und optimieren diese mithilfe digitaler Tools. Aus den Ergebnissen der CO2-Bilanz leiten Sie Potenziale zur Datenverbesserung und zur Reduktion von Emissionen ab. Im Rahmen von Brancheninitiativen arbeiten Sie an Klimaschutzthemen mit und tauschen sich dazu mit Lieferanten aus. Kontinuierlich beobachten und analysieren Sie regulatorische Entwicklungen sowie gesetzliche und marktbezogene [. .. ]
Job am 15.01.2026 bei Jooble gefunden
Element
• Homeoffice
[. .. ] platform, devised primarily for government, defence and public sector organisations. We are a for-profit company that is committed to open source. We build Element on top of [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] an open protocol called Matrix, which was created by the same team that leads Element. Matrix is a not-for-profit open source project. Element works closely with BWI on the Bw Messenger for the German Armed Forces, NATO, the United Nations, Gematik on TI-Messenger for the German healthcare industry, and Germanys [. .. ] respectful and give candidates the best chance to show us what you can do. If we ever fall down on this, please let us know. The role The Product Marketing Manager will own Elements product-related strategy, working closely with the Product and Engineering teams to create accurate, easy to understand sales and marketing collateral. The role reports into the VP of Marketing. Responsibilities Strategy; actively bridge Product, Sales, Engineering, Customer Success, and Marketing teams to create cohesive product strategies, launches [. .. ]
Job am 14.01.2026 bei Jooble gefunden
ICON
Manager, Site Engagement Liaison
• Homeoffice
Work-Life-Balance
As a
Manager, Site Engagement Liaison, you will be joining the worlds largest most comprehensive clinical research organisation, powered by healthcare intelligence. The Site Engagement Liaison Manager is a [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] field based expert who supports the conduct and the patient recruitment of the client global clinical trials at investigative sites, through local and relational [. .. ] providing key country/ regional and site specific knowledge including patient pathways and operational execution. Interface and act as a local client Trial Ops representative, an expert on the clinical trial protocol (s) and SME providing the sites with knowledge and awareness about the current and upcoming clinical trials. Lead and engage in local site, KOL and network engagement initiatives in view of the clinical trials. Contribute to the trial specific site feasibility/ selection strategy and collaborate with the Clinical Trial Team [. .. ]
Job am 14.01.2026 bei Jooble gefunden
Thermo Fisher Scientific
• Homeoffice
[. .. ] PPD CRO and still gain invaluable client dedicated experience. Discover Impactful Work: Accountable for achieving the final clinical deliverable (usually clean data from evaluated patients as specified [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] in the study protocol) within the time period specified in the contract with the customer. Interprets data on project issues and makes good business decisions with support from experienced team members or line manager. Works to ensure that all clinical deliverables meet the customer s time/ quality/ cost expectations. Maintains profitability by ensuring clinical activity is conducted within contract scope, through efficient management of the clinical team. Typically works on projects of low to moderate complexity and as part of a team of CTMs. [. .. ]
Job am 14.01.2026 bei Jooble gefunden
Element
Werkstudent/ Junior Commercial Manager
• Homeoffice
Absolventen, Einsteiger, Trainees Werkstudenten
[. .. ] platform, devised primarily for government, defence and public sector organisations. We are a for-profit company that is committed to open source. We build Element on top of [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] an open protocol called Matrix, which was created by the same team that leads Element. Matrix is a not-for-profit open source project. Element works closely with BWI on the Bw Messenger for the German Armed Forces, NATO, the United Nations, Gematik on TI-Messenger for the German healthcare industry, and Germanys [. .. ] to show us what you can do. If we ever fall down on this, please let us know. The role We are seeking a motivated and detail-oriented Junior Commercial Manager to assist our Account Executives and Solution Architects in managing the day to day operations of the commercial process. This role is essential in ensuring smooth running of the process of selling, customer onboarding as well as hand-over between pre-and post-sales stages, contributing to customer satisfaction and [. .. ]
Job am 14.01.2026 bei Jooble gefunden
IQVIA
• Frankfurt am Main
[. .. ] opportunity to work with one single client and to manage clinical research projects in different therapeutic areas. We currently offer the exciting opportunity to join the team [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] as Local Trial Manager (m/w/d) in full-time and work home-based throughout Germany. Your responsibilities will include: Services rendered will adhere to applicable company s standard operating procedures (SOPs) , work instructions, policies, codes of Good Clinical Practice (GCP) , local regulatory requirements, etc. Prepare or contribute to high level budget [. .. ] research target. Deliver competent vendor management at the country level to support the study and may submit requests for vendor services and support vendor selection. Contribute to patient understanding of protocol and patient safety by contributing to the review of country specific informed consent in accordance with procedural document/ templates. Ensure trial subject safety in that all AEs/ SAEs/ PQCs are reported within the required reporting timelines and documented, as appropriate. Ensure Inspection readiness by maintaining complete, accurate and timely data [. .. ]
Job am 14.01.2026 bei Jooble gefunden
IQVIA
Clinical Trial Manager-Single Sponsor dedicated (m/w/d)
• Frankfurt am Main
[. .. ] clinical research projects in different therapeutic areas and to cooperate closely with one of our key clients. We currently offer the exciting opportunity to join the team [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] as Clinical Trial Manager (m/w/d) in full-time and work home-based throughout Germany. In this role you will be accountable for the operational management of the component of clinical trials. Furthermore, you will need to gain an oversight to assure achievement of trial recruitment commitment, timelines, budget and quality standards. MAIN [. .. ] and CRAs, ensure: o provision of appropriate trial oversight for the trials by monitoring compliance of trial sites and team to GCP, local regulations, customer SOPs, and adherence to trial protocol. o adequate trial supply distribution to sites. o continuous and timely data entry and cleaning, and on time Data Base Lock. o collection of required documents, with timely, complete, and compliant archiving of all relevant documents for the e TMF and CTR Appendices. Identify risks and contingencies and partner with project [. .. ]
Job am 14.01.2026 bei Jooble gefunden
ePages GmbH
Product Manager AI-Driven Commerce (all genders)
• Hamburg
Jobticket
Deine Aufgaben Als Product
Manager bei e Pages gestaltest du die Zukunft des E-Commerce für kleine Unternehmen und Micro-Merchants. Du arbeitest nutzerzentriert und bringst aktiv KI-Potenziale in Produktvision und [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Arbeitsprozesse ein. Dabei verbindest du Markt- und Technologieverständnis, um neue Impulse zu setzen und unser Produkt kontinuierlich weiterzuentwickeln. Du wirst Teil eines erfahrenen Teams [. .. ] strategisch denkender Product Manager, der gerne Verantwortung übernimmt und Themen eigenständig vorantreibt Du begeisterst dich für KI und bist mit modernen Konzepten wie Custom GPTs, KI-Agenten, dem Model Context Protocol (MCP) , Vibe Coding oder ähnlichen AI-gestützten Tools vertraut. Du erkennst früh, wie daraus Mehrwert für Nutzerinnen und Produkt entsteht. Du hast Erfahrung als Product Manager oder Product Owner in der Softwareentwicklung, idealerweise im E-Commerce oder Saa S-Umfeld Du bringst gutes technisches Verständnis mit und kannst gemeinsam mit [. .. ]
Job vor 7 Tagen bei Neuvoo.com gefunden
Techem Metering GmbH
AI Architect (m/f/d) Full-time/ Part-time
• Hessen
[. .. ] English language skills, and communication and presentation know-how Advantageous Experience in integrating AI components into complex IT architectures and workflows Knowledge of Microsoft Azure, AI Foundry, and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Model Context Protocol (MCP) , as well as in building AI agents Hands-on experience with Copilot Studio and low-code/ no-code AI tools Initial experience with MLOps, AI governance, and security aspects of AI deployments Knowledge of enterprise architecture management and technology consulting Career at Techem Your advantages Welcome to the [. .. ] the company pension scheme. Personal development at Techem: Freedom to develop your own creativity and skills, a wide range of opportunities for further development as both a specialist and a manager, such as our systematic development program STEP or a varied seminar program as part of our Techem Academy. Employee well-being: Flexible working hours, mobile working, support in balancing work and family life family (e. g. , childcare, nursing care, mental health with heycare ) , discreet social counseling via [. .. ]
Neu Job vor 6 Std. bei Jooble gefunden
Eurofins
Clinical Project Manager (Permanent)
• Hamburg
Homeoffice möglich
[. .. ] regulatory services and all services for management of Phase I-III drug trials and medical device studies. Eurofins bioskin is headquartered in Hamburg, Germany. We are looking for [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] a Project Manager with comprehensive experience to join our team at Eurofins bioskin in Hamburg. The Project Managers essential function is to organize and manage clinical studies coordinating all involved departments at Eurofins bioskin as well as external stakeholders including being the primary contact person for the sponsor. Management and oversight of further [. .. ] up and maintenance of timelines and tracking tools Set-up and maintenance of trial specific plans and manuals Set-up and maintenance of risk management Interface support for e. g. protocol/ ICF development, feasibility/ site selection, EC/ regulatory submission, TMF maintenance, clinical monitoring Degree in a scientific or medical discipline At least 3 years of experience in the area of clinical trial management or clinical research Very good English skills Home office based work is possible (at least partially office-based [. .. ]
Neu Job vor 6 Std. bei Jooble gefunden
Eurofins
Clinical Project Manager
• Hamburg
Homeoffice möglich
[. .. ] regulatory services and all services for management of Phase I-III drug trials and medical device studies. Eurofins bioskin is headquartered in Hamburg, Germany. We are looking for [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] a Project Manager with comprehensive experience to join our team at Eurofins bioskin in Hamburg. The Project Managers essential function is to organize and manage clinical studies coordinating all involved departments at Eurofins bioskin as well as external stakeholders including being the primary contact person for the sponsor. Management and oversight of further [. .. ] up and maintenance of timelines and tracking tools Set-up and maintenance of trial specific plans and manuals Set-up and maintenance of risk management Interface support for e. g. protocol/ ICF development, feasibility/ site selection, EC/ regulatory submission, TMF maintenance, clinical monitoring Degree in a scientific or medical discipline At least 3 years of experience in the area of clinical trial management or clinical research Very good English skills Home office based work is possible (at least partially office-based [. .. ]
Neu Job vor 6 Std. bei Jooble gefunden
Eurofins
Clinical Trials Project Manager
• Hamburg
Homeoffice möglich
[. .. ] regulatory services and all services for management of Phase I-III drug trials and medical device studies. Eurofins bioskin is headquartered in Hamburg, Germany. We are looking for [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] a Project Manager with comprehensive experience to join our team at Eurofins bioskin in Hamburg. The Project Managers essential function is to organize and manage clinical studies coordinating all involved departments at Eurofins bioskin as well as external stakeholders including being the primary contact person for the sponsor. Management and oversight of further [. .. ] up and maintenance of timelines and tracking tools Set-up and maintenance of trial specific plans and manuals Set-up and maintenance of risk management Interface support for e. g. protocol/ ICF development, feasibility/ site selection, EC/ regulatory submission, TMF maintenance, clinical monitoring Degree in a scientific or medical discipline At least 3 years of experience in the area of clinical trial management or clinical research Very good English skills Home office based work is possible (at least partially office-based [. .. ]
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Häufig gestellte Fragen
Wieviel verdient man als Protocol manager pro Jahr?
Als Protocol manager verdient man zwischen EUR 60.000,- bis EUR 90.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Protocol Manager Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 178 offene Stellenanzeigen für Protocol Manager Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Protocol Manager Jobs?
Aktuell suchen 38 Unternehmen nach Bewerbern für Protocol Manager Jobs.
Welche Unternehmen suchen nach Bewerbern für Protocol Manager Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Protocol Manager Stellenangebote:
- Bristol Myers Squibb (9 Jobs)
- Alimentiv (7 Jobs)
- Abb Vie (6 Jobs)
- Thermo Fisher Scientific (6 Jobs)
- Ventura TRAVEL (5 Jobs)
- IQVIA (5 Jobs)
In welchen Bundesländern werden die meisten Protocol Manager Jobs angeboten?
Die meisten Stellenanzeigen für Protocol Manager Jobs werden derzeit in Berlin (22 Jobs), Baden-Württemberg (18 Jobs) und Bayern (17 Jobs) angeboten.
Zu welchem Berufsfeld gehören Protocol Manager Jobs?
Protocol Manager Jobs gehören zum Berufsfeld Netzwerke.
