157 Jobs für Data Investigator
Stellenangebote Data Investigator Jobs
Job gestern bei StepStone gefunden
Sigmund Freud Privatuniversität Wien
• Wien
[. .. ] researchers and medical specialists. The mission of medical research at SFU is to foster innovation in healthy aging and preventive medicine across all fields of human medicine. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] We actively support investigator-initiated clinical studies and translational research within SFU and its partner hospitals, as well as collaborative projects with external senior scientists, always with the goal of translating research outcomes directly into patient care. Our laboratories are equipped with a broad range of state-of-the-art instruments supporting molecular and [. .. ] field. Demonstrated experience in leading an interdisciplinary molecular biology research team. Experience in supervising Ph D students and other trainees. Strong expertise in modern molecular biology and biochemical techniques, with excellent data management skills. Experience integrating translational research into clinical studies. Proven record of successful grant applications. Excellent organizational, leadership, and problem-solving skills. Proactive, solution-oriented mindset with a collaborative approach. Fluency in English, both written and spoken; German proficiency is an advantage. We are seeking a Full Professor of Molecular [. .. ]
Job vor 2 Tagen bei StepStone gefunden
Miltenyi Biotec B. V. Co. KG
Lead Medical Writer (m f d)
• Bergisch Gladbach
Führungs-/ Leitungspositionen Homeoffice möglich
[. .. ] review, revision and finalization of clinical documents for submission to regulatory authorities. You lead the development, authoring, and submission of regulatory documents (e. g. , CTD modules, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] clinical study reports, investigator brochures, INDs/ IMPDs, NDAs/ MAAs, and briefing documents) . Your responsibility includes ensuring that all documents are scientifically sound, strategically aligned, and compliant with global regulatory standards. In addition, you manage document timelines, coordinate internal reviews, and ensure on-time delivery. Collaborating closely within cross-functional teams (clinical, regulatory, biostatistics, [. .. ] proven experience in medical writing within clinical development with a strong focus on regulatory writing. As an expert in your field, you possess in-depth knowledge of ICH guidelines and data protection laws relevant to medical writing and you are experienced in setting up standards and processes. You have a strong track record of authoring and managing key regulatory submission documents; experience with MAA/ BLA submissions is a plus. Experience with ATMPs/ CAR-T treatments, oncology/ hematology or autoimmune diseases is [. .. ]
Job am 27.11.2025 bei Mindmatch.ai gefunden
Universität Wien
• AT- 9 Wien
Homeoffice möglich
Work-Life-Balance
[. .. ] doc in the Austrian university system) , you will work for the ERC project The anthropology of the future: an art world perspective (ANTHROFUTURE) led by Prof. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Manuela Ciotti (Principal investigator, PI) . The project is based at the Department of Social and Cultural Anthropology. As part of the Faculty of Social Sciences, the Department of Social and Cultural Anthropology not only brings together renowned scientists and students, but also different research areas, a variety of ethnographic methods, a large number [. .. ] ANTHROFUTURE and will be expected to:Finalize your dissertation agreement within 12 months Work on your dissertation and its completion within 3 years Carry out research in full compliance of ethics, data-and best-practice ERC research guidelines (you will receive support in doing that) Develop and deliver high-quality, innovative research outcomes on the topic of the research project Participate in conferences of appropriate learned societes and associations Produce research publications for leading international and/or peer reviewed journals and book [. .. ]
Job vor 10 Tagen bei Jobleads gefunden
Senior/ Medical Director (Ophthalmology)
• Hamburg
Führungs-/ Leitungspositionen
[. .. ] innovative professionals to ensure our customers achieve their goals. Key Responsibilities Expert Guidance : Provide advanced medical input on study design, measurement strategies, and trial protocols, including [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] safety sections and investigator brochures. Comprehensive Safety Oversight : Review safety data such as adverse events, labs, vital signs, ECGs, and clinical trial reports from a medical perspective. Regulatory Risk Support : Conduct senior-level medical reviews of individual cases, cumulative listings, PSURs, PBRERs, DSURs, and Risk Management Plans. Medical Monitoring Signal Detection : Serve as a medical monitor in trials, perform [. .. ]
Job am 04.12.2025 bei Jobleads gefunden
• München, Bayern
Führungs-/ Leitungspositionen
[. .. ] innovative professionals to ensure our customers achieve their goals. Key Responsibilities Expert Guidance : Provide advanced medical input on study design, measurement strategies, and trial protocols, including [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] safety sections and investigator brochures. Comprehensive Safety Oversight : Review safety data such as adverse events, labs, vital signs, ECGs, and clinical trial reports from a medical perspective. Regulatory Risk Support : Conduct senior-level medical reviews of individual cases, cumulative listings, PSURs, PBRERs, DSURs, and Risk Management Plans. Medical Monitoring Signal Detection : Serve as a medical monitor in trials, perform [. .. ]
Job am 23.11.2025 bei Jobleads gefunden
Medical Science Liaison Manager, Nephrology, North-West
• München, Bayern
[. .. ] medical community with up-to-date medical and scientific information Identify and execute collaboration opportunities between expert KOLs in nephrology and Alexion medical affairs and clinical development such as [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] publications, investigator-initiated trials, regional advisory boards, training and speaker development programs. Communicate experts opinion, feedback on new data and clinical trends to Alexion Medical Affairs, therapeutic area (TA) franchises and translate this information into strategic recommendations to enhance science and advance patient care. Respond to unsolicited medical information requests in the region, manage questions, liaise with headquarters to ensure proper response has been provided and ensure that data [. .. ]
Job am 23.11.2025 bei Jobleads gefunden
• München, Bayern
[. .. ] medical community with up-to-date medical and scientific information Identify and execute collaboration opportunities between expert KOLs in nephrology and Alexion medical affairs and clinical development such as [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] publications, investigator-initiated trials, regional advisory boards, training and speaker development programs. Communicate experts opinion, feedback on new data and clinical trends to Alexion Medical Affairs, therapeutic area (TA) franchises and translate this information into strategic recommendations to enhance science and advance patient care. Respond to unsolicited medical information requests in the region, manage questions, liaise with headquarters to ensure proper response has been provided and ensure that data [. .. ]
Job am 10.10.2025 bei Jobleads gefunden
Medical Science Liaison
• München, Bayern
Firmenwagen 30+ Urlaubstage
[. .. ] Identifying, developing, and maintaining professional relationships with national/ regional KOLs, establishing peertopeer collaborations with key medical experts in the therapeutic areas covered by Pharmanovia. Supporting evidence generation [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] initiatives including potential investigator site identification, trial recruitment, registries, and presentation of final approved data, involving experts to generate scientific data including investigatorinitiated trials. Collaborating with physicians on medical affairs initiatives including publication and communication plans, advisory boards, medical education opportunities, webinars, training, and speaker development. Serving as a scientific peertopeer resource to external disease experts and internal stakeholders. Supporting the medical community with uptodate [. .. ]
Job am 27.06.2025 bei Jobleads gefunden
Führungs-/ Leitungspositionen
[. .. ] and answering complex questions related to medical, legal, and regulatory concerns. Responsibilities Expert Guidance: Provide advanced medical input on study design, measurement strategies, and trial protocols, including [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] safety sections and investigator brochures. Comprehensive Safety Oversight: Review safety data such as adverse events, labs, vital signs, ECGs, and clinical trial reports from a medical perspective. Regulatory Risk Support: Conduct senior-level medical reviews of individual cases, cumulative listings, PSURs, PBRERs, DSURs, and Risk Management Plans. Medical Monitoring Signal Detection: Serve as a medical monitor in trials, perform literature reviews, [. .. ]
Neu Job vor 3 Std. bei Jobleads gefunden
Site Relationship Manager
• Essen, Nordrhein- Westfalen
[. .. ] Support development of countryspecific plans to engage advocacy groups and enhance recruitment. Attend local medical/ support group meetings and conferences. Collaborate with internal teams and CROs to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] ensure quality feasibility data and effective site selection. Provide input on sitelevel recruitment targets and strategies. Understand and support compliance with local regulatory and ethics requirements. Creating and Maintaining Strong Site Relationships Build and maintain strong relationships with site personnel to enable timely trial delivery. Conduct motivation visits to encourage engagement and recruitment. Partner [. .. ] 5 years of experience as a Clinical Research Associate, Monitor, or similar role. Proven clinical research and site management experience within Pharma, Biotech, or CRO settings. Direct experience collaborating with investigator sites and investigators. Strong knowledge of ICH GCP guidelines. Demonstrated ability to build and maintain site relationships both inperson and remotely. Excellent networking, communication, and problemsolving skills. Experience in rare diseases and endocrinology What We Offer We provide a competitive compensation package, comprehensive benefits, and the opportunity for personal and [. .. ]
Neu Job vor 3 Std. bei Jobleads gefunden
[. .. ] site team members, related to study drug and pipeline compounds/ clinical trial design/ rationale, using client developed and approved resources If requested, keep up to date with [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] clinical knowledge, published data and trial work for client and competitive product studies If requested, support relevant education at Site Investigator Meetings, including Site Initiation Visits, in line with clinical study plans Develop strong communication links with PIs and study physicians and their teams Ensure requests received from PIs are managed efficiently and effectively, and that the client studies are the primary focus of the study site support teams Act as [. .. ]
Neu Job vor 3 Std. bei Jobleads gefunden
Medical Science Liaison, Immunology (IBD) , Germany
Work-Life-Balance
[. .. ] meetings Sharing important clinical and scientific insights that you have gathered from fieldwork to cross-functional teams Acting as an internal and external scientific expert Adhering to compliance [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] requirements Supporting investigator-initiated studies What youll need to be successful: An advanced doctoral degree (MD, Ph D, Pharm D) is preferred Relevant therapeutic area knowledge in the field of immunology or immuno-oncology, experience in gastroenterology is a plus. Post graduate therapeutic area experience is preferred Fluency in English and local language 3+ [. .. ] MSL and/or headquartered based medical affairs role and clinical trial background Demonstrable experience in building and maintaining relationships with KOLs Ability to effectively communicate and assimilate scientific and clinical data to the relevant audience Biotech experience is a plus Willing and able to travel internationally, up to 70 of time We are an equal opportunities employer:We encourage and support equal employment opportunities for all applicants and are determined to ensure that no applicant receives less favourable treatment due to their gender, [. .. ]
Job gestern bei Jobleads gefunden
• Genf
Führungs-/ Leitungspositionen
[. .. ] will conduct in-depth investigations and manage fraud risk assessments while contributing to the companys ethical standards. Candidates should have a minimum of five years of audit experience [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and strong data analytics skills. The role demands fluency in English and may involve international travel. #J-18808-Ljbffr 73088414 [. .. ]
Job gestern bei Jobleads gefunden
(Junior-) Field Medical Advisor-Rare Oncology South
• München, Bayern
Absolventen, Einsteiger, Trainees
[. .. ] issues. The primary role is to deliver and facilitate medical education and communications, research, and scientific insight gathering activities of the client. This includes the provision of [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] scientific and medical data on both licensed and unlicensed products and indications as permissible by local laws and regulations. Responsibilities Develop and maintain, in a self-driven manner, outstanding knowledge of immuno-oncology and relevant disease areas in addition to client and competitor product knowledge Maintain an in-depth understanding of the medical strategy [. .. ] aligned to strategy within the business Serves as external, credible scientific expert on disease area and client products at HCP field meetings, key medical and scientific conferences, advisory boards, clinical investigator meetings and patient advocacy group meetings Identify key field insights related to client products, activities and the disease area and effectively disseminate and collaborate with cross-functional partners Facilitate clear communication between the business and investigators in investigator engagement for both client trials and investigator-sponsored studies and barriers to [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
• München, Bayern
Führungs-/ Leitungspositionen
[. .. ] learn more. Base pay range Responsible for the clinical operations of a project within a defined regional/ global level. Provides oversight of project deliverables, assigned Clinical Research [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Associate (CRAs) and Investigator sites in accordance with 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 [. .. ] the site/ CRA in the satisfactory performance and compliance with standards mentioned above May support clinical project team by providing oversight of study deliverables related to other departments (e. g. Data Management, TMF Operations, etc. ) Oversee regional startup and feasibility activities Assist in vendor management activities as required per project Perform review of visit reports for quality, compliance and appropriate site management Assure compliance with high quality and timely project deliverables according to the project requirements and the monitoring plan [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
Medical Science Liaison NM-Asia Pacific
• Gemeinde Au, Vorarlberg
[. .. ] patients. Generate and execute tactical regional plans to provide needs based, value-added support of the medical and scientific community in line with company goals. Support clinical development [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] initiatives including investigator-initiated research (IIR) and Liva Nova-sponsored clinical studies and registries (e. g. , site identification, trial recruitment, and presentation of final approved data) . Collaborate with key internal and external stakeholders on Medical Affairs-led initiatives including publications, advisory boards, medical education (e. g. , CME) opportunities, training, and speaker development. Identify, profile, prioritize and map thought leaders in line with strategic initiatives and goals. Support external stakeholders with up-to-date medical [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
• Hamburg
[. .. ] Support development of countryspecific plans to engage advocacy groups and enhance recruitment. Attend local medical/ support group meetings and conferences. Collaborate with internal teams and CROs to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] ensure quality feasibility data and effective site selection. Provide input on sitelevel recruitment targets and strategies. Understand and support compliance with local regulatory and ethics requirements. Creating and Maintaining Strong Site Relationships Build and maintain strong relationships with site personnel to enable timely trial delivery. Conduct motivation visits to encourage engagement and recruitment. Partner [. .. ] 5 years of experience as a Clinical Research Associate, Monitor, or similar role. Proven clinical research and site management experience within Pharma, Biotech, or CRO settings. Direct experience collaborating with investigator sites and investigators. Strong knowledge of ICH GCP guidelines. Demonstrated ability to build and maintain site relationships both inperson and remotely. Excellent networking, communication, and problemsolving skills. Experience in rare diseases and endocrinology. What We Offer We provide a competitive compensation package, comprehensive benefits, and the opportunity for personal and [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
Clinical Operations Lead
• Düsseldorf, Nordrhein- Westfalen Duesseldorf
Führungs-/ Leitungspositionen
Clinical Operations Lead Responsible for the clinical operations of a project within a defined regional/ global level. Provides oversight of project deliverables, assigned Clinical Research Associate (CRAs) and
Investigator [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] sites in accordance with 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 [. .. ] the site/ CRA in the satisfactory performance and compliance with standards mentioned above May support clinical project team by providing oversight of study deliverables related to other departments (e. g. Data Management, TMF Operations, etc. ) Oversee regional startup and feasibility activities Assist in vendor management activities as required per project Perform review of visit reports for quality, compliance and appropriate site management Assure compliance with high quality and timely project deliverables according to the project requirements and the monitoring plan [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
Clinical Operations Lead
• Köln, Nordrhein- Westfalen Koeln
Führungs-/ Leitungspositionen
[. .. ] Westphalia, Germany Clinical Operations Lead Responsible for the clinical operations of a project within a defined regional/ global level. Provides oversight of project deliverables, assigned Clinical Research [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Associate (CRAs) and Investigator sites in accordance with 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 [. .. ] the site/ CRA in the satisfactory performance and compliance with standards mentioned above May support clinical project team by providing oversight of study deliverables related to other departments (e. g. Data Management, TMF Operations, etc. ) Oversee regional startup and feasibility activities Assist in vendor management activities as required per project Perform review of visit reports for quality, compliance and appropriate site management Assure compliance with high quality and timely project deliverables according to the project requirements and the monitoring plan [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
(Senior) Director Clinical Development
• München, Bayern
Führungs-/ Leitungspositionen
[. .. ] the clinical development strategy for the assigned product. Specific responsibilities include design of clinical trials across all phases (including phase IV) , clinical protocol development, medical monitoring, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] analysis of study data, and contribution to clinical study reports, registration dossier modules and briefing books for Health Authority interactions. The Director will represent and defend the clinical strategy during regulatory review processes (MAA) across multiple geographies and in meetings with Health Authorities. The role requires close collaboration with other research and development functions, [. .. ] teams, regulatory, safety and other crossfunctional teams. Act as study physician for Sobi-sponsored studies: develop study synopsis and protocols, contribute to statistical analysis plans, perform medical monitoring, participate in investigator meetings and review other key clinical documents. Interact with key opinion leaders and patient representatives, lead advisory boards to define clinical strategy and inform trial design. Provide strategic and operational clinical development expertise in interactions with regulatory and reimbursement authorities. Contribute highquality scientific and medical input to regulatory submissions, responses [. .. ]
Job vor 3 Tagen bei Jobleads gefunden
Site Relationship Manager
• Kassel, Hessen
[. .. ] Support development of countryspecific plans to engage advocacy groups and enhance recruitment. Attend local medical/ support group meetings and conferences. Collaborate with internal teams and CROs to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] ensure quality feasibility data and effective site selection. Provide input on sitelevel recruitment targets and strategies. Understand and support compliance with local regulatory and ethics requirements. Creating and Maintaining Strong Site Relationships Build and maintain strong relationships with site personnel to enable timely trial delivery. Conduct motivation visits to encourage engagement and recruitment. Partner [. .. ] 5 years of experience as a Clinical Research Associate, Monitor, or similar role. Proven clinical research and site management experience within Pharma, Biotech, or CRO settings. Direct experience collaborating with investigator sites and investigators. Strong knowledge of ICH GCP guidelines. Demonstrated ability to build and maintain site relationships both inperson and remotely. Excellent networking, communication, and problemsolving skills. Experience in rare diseases and endocrinology. What We Offer We provide a competitive compensation package, comprehensive benefits, and the opportunity for personal and [. .. ]
Job vor 4 Tagen bei Jobleads gefunden
SAS Data Engineer/ ETL-Developer Stellendetails DKB Das kann Bank
• Berlin
Abgeschlossenes Studium
SAS
Data Engineer/ ETL-Developer Stellendetails DKB Das kann Bank Du bist Teil eines Teams innerhalb der DKB, das sich mit analytischer Fraud Prevention Detection beschäftigt Du wirkst im Rahmen [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] deiner Tätigkeit bei der Entwicklung, Umsetzung und Anpassung von ETL-Jobs und Modulen mit Du unterstützt bei der Definition, Implementierung und dem [. .. ] (Ab Initio, SAS Base, SQL, XML, HTML) und der Datenmodellierung bzw. statischer Datenanalysen Du bringst idealerweise Erfahrungen mit SAS-Tools (DI-Studio, Enterprise Miner, Enterprise Guide, SAS Viya, SAS Visual Investigator) mit Eine selbstständige Arbeitsweise und sehr gute konzeptionelle und analytische Fähigkeiten zeichnen dich aus Du bist strukturiert und suchst nach Lösungen, nicht nach Problemen Du bist durchsetzungsstark und kannst die Perspektive anderer einzunehmen Dir macht es Spaß, Neues zu lernen Die DKB steht für Vielfalt und Chancengerechtigkeit. Egal, woher du [. .. ]
Job vor 4 Tagen bei Jobleads gefunden
Clinical Trial Project Manager
[. .. ] Manager to oversee the execution of international clinical trials in the field of neurodegenerative and ophthalmologic diseases. Your Responsibilities Drafting and reviewing clinical trial documents, including study [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] protocols, patient information, investigator brochures, study plans, manuals, and reports End-to-end execution of clinical trials, including comprehensive monitoring activities from study start-up through close-out Development of deviation plans; defining and assessing protocol deviations at patient, site, and study level, and recommending follow-up actions Providing clinical expertise and conducting risk/ [. .. ] Contributing to the selection of clinical service providers Reviewing and tracking study documents for regulatory submissions Supporting audits and inspections (GCP) , and contributing to CAPA development and implementation Reviewing data management documents (e. g. , DMP, DVP) and biostatistics documents (e. g. , SAP, TFL) Coordinating study logistics including medication, samples, materials, and managing the Trial Master File Monitoring and analyzing clinical study data Preparing and delivering internal and external presentations Conducting trainings related to study processes and procedures Supporting [. .. ]
Job vor 5 Tagen bei Jobleads gefunden
CRA Germany or Austria-single-client
• München, Bayern
Beratungs-/ Consultingtätigkeiten
[. .. ] performed and documented for each subject/ patient, as required/appropriate. Demonstrates diligence in protecting the confidentiality of each subject/ patient. Assesses factors that might affect subject/ patients safety [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and clinical data integrity at an investigator/ physician site such as protocol deviation/ violations and pharmacovigilance issues. Per the Clinical Monitoring/ Site Management Plan (CMP/ SMP) : Assesses site processes. Conducts Source Document Review of appropriate site source documents and medical records. Verifies required clinical data entered in the case report form (CRF) is accurate and complete. [. .. ]
Job vor 5 Tagen bei Jobleads gefunden
Site Relationship Manager
• Mainz, Rheinland- Pfalz
[. .. ] Support development of countryspecific plans to engage advocacy groups and enhance recruitment. Attend local medical/ support group meetings and conferences. Collaborate with internal teams and CROs to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] ensure quality feasibility data and effective site selection. Provide input on sitelevel recruitment targets and strategies. Understand and support compliance with local regulatory and ethics requirements. Creating and Maintaining Strong Site Relationships Build and maintain strong relationships with site personnel to enable timely trial delivery. Conduct motivation visits to encourage engagement and recruitment. Partner [. .. ] 5 years of experience as a Clinical Research Associate, Monitor, or similar role. Proven clinical research and site management experience within Pharma, Biotech, or CRO settings. Direct experience collaborating with investigator sites and investigators. Strong knowledge of ICH GCP guidelines. Demonstrated ability to build and maintain site relationships both inperson and remotely. Excellent networking, communication, and problemsolving skills. Experience in rare diseases and endocrinology What We Offer We provide a competitive compensation package, comprehensive benefits, and the opportunity for personal and [. .. ]
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Häufig gestellte Fragen
Wieviel verdient man als Data Investigator pro Jahr?
Als Data Investigator verdient man zwischen EUR 35.000,- bis EUR 50.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Data Investigator Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 157 offene Stellenanzeigen für Data Investigator Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Data Investigator Jobs?
Aktuell suchen 18 Unternehmen nach Bewerbern für Data Investigator Jobs.
Welche Unternehmen suchen nach Bewerbern für Data Investigator Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Data Investigator Stellenangebote:
- Tigermed (20 Jobs)
- Veeda Lifesciences (11 Jobs)
- Tubulis GmbH (11 Jobs)
- TFS Health Science (10 Jobs)
In welchen Bundesländern werden die meisten Data Investigator Jobs angeboten?
Die meisten Stellenanzeigen für Data Investigator Jobs werden derzeit in Bayern (26 Jobs), Nordrhein-Westfalen (25 Jobs) und Niedersachsen (17 Jobs) angeboten.
Zu welchem Berufsfeld gehören Data Investigator Jobs?
Data Investigator Jobs gehören zum Berufsfeld Datenbanken.
