136 Jobs für Data Investigator
Stellenangebote Data Investigator Jobs
Job am 27.01.2026 bei Neuvoo gefunden
Dabster
• Hamburg
[. .. ] Performance Tools for i and IBM i Performance Navigator Tuning Tune system parameters SQL queries and indexes to optimize performance using IBM i SQL Performance Analyzer and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] IBM i Performance Data Investigator Backup and Recovery: Backups Regularly back up systems to ensure data protection and disaster recovery using tools like BRMS and IBM i Save Restore Recovery Restore systems from backups and resolve data corruption issues using BRMS and IBM i Recovery Tools Data Integrity Data Modeling Work with data architects to [. .. ]
Job vor 2 Tagen bei StepStone gefunden
Dr. Falk Pharma GmbH
Medical Lead in Clinical Research (m/f/d)
• Freiburg
Führungs-/ Leitungspositionen Homeoffice möglich
[. .. ] execution for assigned projects in collaboration with Clinical Research teams and other cross-functional stakeholders. Key Responsibilities Provides medical input to Clinical Trial Protocol, Investigators Brochure, Informed Consent [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Form, Independent Data Monitoring Committee Charter, Statistical Analysis Plan, Medical Monitoring Plan, Clinical Trial Report, Clinical Trial Overview Statements and other clinical trial documents Provides medical risk assessment for activities related to clinical trials and development programs Performs oversight for clinical trial medical monitoring activities outsourced to CROs Point of contact for sites [. .. ] medical expertise in the review of adverse events and safety issues, as requested Provides support in the review of scientific publications (abstracts, presentations, and manuscripts) Supports review of concepts for investigator-initiated studies Contributes to company-internal process improvement initiatives (e. g. SOP updates) Your qualification Physician/ medical license holder A minimum of 5 years of clinical development research, or related clinical research experience within the industry (pharmaceutical, biotech, CRO) at an international (Europe, USA, Australia) level is required Knowledge in [. .. ]
Neu Job vor 4 Std. bei Mindmatch.ai gefunden
Syneos Health
• AT- 9 Wien
[. .. ] ability to perform activities for assigned sites working with study start-up and regulatory. Conduct of all remote and on-site monitoring activities through all study stages. Routinely reviews [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] the Investigator Site File (ISF) for accuracy, timeliness and completeness. Reconciles contents of the ISF with the Trial Master File (TMF) . Ensures the investigator/ physician site is aware of the requirement of archiving essential documents in accordance with local guidelines and regulations. Documents activities via confirmation letters, follow-up letters, trip reports, communication logs, and other required project documents as per SOPs and SMP, within required timelines. Supports subject/ patient recruitment, retention and awareness strategies. Enters data into tracking systems as required to track all observations, ongoing status and assigned action items to resolution. Demonstrates diligence in protecting the confidentiality of each subject/ patient. Assigned sites data review, assisting with data query resolution and missing data follow-up (only as applicable) . Review data using data trend [. .. ]
Job vor 3 Tagen bei Mindmatch.ai gefunden
Euraxess
Postdoctoral Researcher (quantitative) Refugees (Im) Mobilities Political Agency (m/f/d)
• AT- 9 Wien
Homeoffice möglich
[. .. ] and Germany) . The project will collect a cross-national survey, life histories, online interviews, and a compilation of humorous representations of the state. The team consists of [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] the Principal Investigator (PI) , two postdoctoral researchers, a Ph D researcher, a project manager, and local research assistants. The quantitative postdoctoral researcher will co-lead the quantitative data collection together with the PI and lead the case study on South Sudan. You will be involved in the development of the survey questionnaire, train and supervise enumerators during data collection and analyse the survey data. The quantitative postdoctoral researcher will also be involved in the analysis of the survey [. .. ]
Job vor 3 Tagen bei Mindmatch.ai gefunden
Planet
• AT- 3 St. Pölten
Homeoffice möglich
[. .. ] constellation delivers an unprecedented dataset of empirical information via a revolutionary cloud-based platform to authoritative figures in commercial, environmental, and humanitarian sectors. We are both a space [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] company and data company all rolled into one. Customers and users across the globe use Planets data to develop new technologies, drive revenue, power research, and solve our worlds toughest obstacles. As we control every component of hardware design, manufacturing, data processing, and software engineering, our office is a truly inspiring mix of [. .. ] error budgets, and calibration concepts for our highresolution and nextgeneration monitoring programs, ensuring spatial integrity across diverse fleets. Additionally, you will drive ongoing performance characterization and serve as a lead investigator for complex image quality issuestroubleshooting sensor models and geometric anomalies to architect the longterm fixes that maintain Planets high standard of spatial data. This is a fulltime, remote position based in Austria. If located near an office, you are expected to work from that office 3 days per week. Impact [. .. ]
Job vor 7 Tagen bei Mindmatch.ai gefunden
Milestone One
Clinical Site Coordinator
• AT- 9 Wien
[. .. ] support the medical site and CRO/ Sponsor team in meeting project timelines and enrollment goals. Maintain study specific and general tracking of documents at the site level. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Accurate and timely data entry into study specific EDC systems and timely resolution of data clarification queries issued for the site. Timely reporting and follow up on Reportable Adverse Events and Protocol Deviations. Proper handling, accountability and reconciliation of investigational products and clinical supplies. Collect, handle and maintain all sitespecific regulatory documents as needed. Facilitate and support the contract and budget negotiations at the site level. Support Investigator and Site payments and processes as needed. Schedule and/or perform study procedures as per study requirements and delegation of responsibilities. Prepare for and participate in onsite study audits or regulatory agency inspections. Qualifications A university degree in Life Science, preferably in pharmacy, nursing or lab analytics. Minimum of 2 [. .. ]
Job vor 9 Tagen bei Mindmatch.ai gefunden
Interdisciplinary Transformation University (IT:U)
• AT- 4 Linz
Werkstudenten
[. .. ] event-based cameras) for Cube Sats. Hardware-software co-design of Cube Sat subsystems for energy-efficient operation in constrained environments. Onboard embedded AI and real-time processing for intelligent
data [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] selection and compression. Development of low-power architectures and novel materials for compact and reliable sensing platforms. Optimization of payload and sensor node design for Earth observation missions. Experimental validation on prototypes and lab-based Cube Sat demonstrators. This project offers the opportunity to contribute to the next generation of [. .. ] and masters transcript of records Motivational letter Up to 3 contacts of professors/ collaborators for recommendations For clarifications regarding the position or the application process, candidates may contact the principal investigator at prior to submitting their application. Please note that questions should ONLY concern aspects not clearly addressed in the call text (if any) . Questions regarding the suitability of a candidate or the evaluation of CVs will not be addressed. All applications, including CVs and supporting documents, must be submitted [. .. ]
Job vor 12 Tagen bei Mindmatch.ai gefunden
PSI CRO
Clinical Site Coordinator
• AT- 9 Wien
[. .. ] and actively supportthe medical site and CRO/ Sponsor team in meeting project timelines and enrollment goals. Maintainstudy specific and general tracking of documents at the site level. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Accurate and timely data entry into study specific EDC systems and timely resolution of data clarification queries issued for the site. Timely reporting and follow up on Reportable Adverse Events and Protocol Deviations. Proper handling, accountability and reconciliation of investigational products and clinical supplies. Collect, handleand maintainall site-specific regulatory documents as needed. Facilitateand support the contract and budget negotiations at the site level. Support Investigator and Site payments and processes as needed. Scheduleand/or performstudy procedures as per study requirements and delegation of responsibilities. Preparefor and participatein onsite study audits or regulatory agency inspections. Qualifications A university degree in Life Science, preferably in pharmacy, nursing or lab analytics. Minimum of 2 years of on-the-[. .. ]
Job am 06.03.2026 bei Mindmatch.ai gefunden
Alimentiv
• AT- 9 Wien
[. .. ] Research Associate I/ II Support/ conduct (as appropriate) site management through remote and supervised onsite visits (initiation, monitoring, and close-out) in compliance with SOPs, protocol, and GCP. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Perform remote data and system reviews (EDC, CTMS, RBM, TMF) to ensure data quality, completeness, and regulatory compliance. Assist/ lead (as appropriate) with query resolution, safety reviews, and adverse event follow-up throughout the study lifecycle. Support/ conduct (as appropriate) site startup and activation activities, including investigator coordination, trial material delivery, and recruitment support. Maintain accurate, timely, and complete TMF documentation, requesting updates as required. Provide day-to-day operational support to Senior CRA, and Lead CRAs. Participate in training, study meetings, and CRA development activities, building competencies required for role progression. Sr. Clinical Research Associate As [. .. ]
Job am 02.03.2026 bei Mindmatch.ai gefunden
Syneos Health
CRA single sponsor-Germany
• AT- 9 Wien
[. .. ] 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. For 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 am 23.02.2026 bei Mindmatch.ai gefunden
Takko Mode Markt GmbH
• AT- 4 Linz
[. .. ] Clinical Research (SCCR) des Kepler Universitätsklinikums Organisation und Koordination von Diagnostik, Labor, Probenversand und gegebenenfalls Prüfmedikation Vorbereitung und Begleitung von Monitorbesuchen, Audits und Behördeninspektionen Kommunikation mit Sponsor [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] innen, Studienzentralen, Principal Investigator innen, Behörden, Ethikkommission, etc Teilnahme an nationalen und internationalen Investigator innen Meetings Mitarbeit an sozial- und wirtschaftswissenschaftlichen Forschungsinfrastrukturen (u. a. AUSSDA The Austrian Social Science Data Archive, ISSP/ SSÖ Sozialer Survey Österreich, GGP. at Gender and Generations Programme Austria und Digital Skills Austria) Aufbereitung und Dokumentation von Forschungsdaten und Metadaten mittels Statistiksoftware Unterstützung bei wissenschaftlichen Projekten, Publikationen und Forschungsanträgen Tätigkeiten im Bereich Science-to-Public-Kommunikation Der konkrete Arbeitsschwerpunkt zwischen Lab-Leitung und Mitarbeiter in gemeinsam [. .. ]
Job am 22.02.2026 bei Mindmatch.ai gefunden
Syneos Health, Inc.
CRA Germany or Austria-single-client
• AT- 9 Wien
[. .. ] 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 am 22.02.2026 bei Mindmatch.ai gefunden
Syneos Health, Inc.
• AT- 9 Wien
[. .. ] 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 am 22.02.2026 bei Mindmatch.ai gefunden
IQVIA
Senior Director, Medical Strategy Lead-Dermatology
• AT- 9 Wien
Führungs-/ Leitungspositionen
[. .. ] the IQVIA Dermatology portfolio through scientific and clinical expertise. The Medical Strategy Lead will be charged with using his/ her clinical, scientific, and operational knowledge to harness [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] the vast IQVIA data and clinical trial resources to develop innovative, data-driven, and patient-centered solutions for Dermatology trials. The Medical Strategy Lead will provide senior clinical and scientific expertise to all IQVIA divisions as requested and will collaborate closely with indication-specific teams to develop integrated strategies for Dermatology. The Medical Strategy [. .. ] design/ clinical development plan, mining data to address important clinical questions relevant to the study, reviewing the protocol for scientific/ regulatory soundness and feasibility, identification of target site and principal investigator profiles, anticipated patient recruitment, standard of care and competitive landscape. Support preparation of customer and bid defense meetings, e. g. training and preparation of the assigned project team; provide specific content; ensure presentation focus and content effectively conveys strategy. Attends and presents at customer meeting, or bid defense or partnership [. .. ]
Job am 31.01.2026 bei Mindmatch.ai gefunden
Universitätsbibliothek der Humboldt- Universität zu Berlin
• 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 [. .. ] 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 am 19.01.2026 bei Mindmatch.ai gefunden
IQVIA
Senior Director, Medical Strategy Lead-Cardiologist
• AT- 9 Wien
Führungs-/ Leitungspositionen
[. .. ] the IQVIA Cardiovascular portfolio through scientific and clinical expertise. The Medical Strategy Lead will be charged with using his/ her clinical, scientific, and operational knowledge to harness [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] the vast IQVIA data and clinical trial resources to develop innovative, data-driven, and patient-centered solutions for Cardiovascular trials. The Medical Strategy Lead will provide senior clinical and scientific expertise to all IQVIA divisions as requested and will collaborate closely with indication-specific teams to develop integrated strategies for Cardiovascular clinical trials, mostly [. .. ] design/ clinical development plan, mining data to address important clinical questions relevant to the study, reviewing the protocol for scientific/ regulatory soundness and feasibility, identification of target site and principal investigator profiles, anticipated patient recruitment, standard of care and competitive landscape. Support preparation of customer and bid defense meetings, e. g. training and preparation of the assigned project team; provide specific content; ensure presentation focus and content effectively conveys Cardiovascular strategy. Attends and presents at customer meeting, or bid defense or [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
• Zug
[. .. ] support the medical site and CRO/ Sponsor team in meeting project timelines and enrollment goals. Maintain study specific and general tracking of documents at the site level. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Accurate and timely data entry into study specific EDC systems and timely resolution of data clarification queries issued for the site. Timely reporting and follow up on Reportable Adverse Events and Protocol Deviations. Proper handling, accountability and reconciliation of investigational products and clinical supplies. Collect, handle and maintain all sitespecific regulatory documents as needed. Facilitate and support the contract and budget negotiations at the site level. Support Investigator and Site payments and processes as needed. Schedule and/or perform study procedures as per study requirements and delegation of responsibilities. Prepare for and participate in onsite study audits or regulatory agency inspections. Build and sustain longlasting relationships with existing and potential clients (sponsors, CROs, medical institutions) . Qualifications College [. .. ]
Job am 10.03.2026 bei Jobleads gefunden
Senior Director, Medical Strategy Lead-Cardiologist
• Frankfurt, Hesse
Führungs-/ Leitungspositionen
[. .. ] the IQVIA Cardiovascular portfolio through scientific and clinical expertise. The Medical Strategy Lead will be charged with using his/ her clinical, scientific, and operational knowledge to harness [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] the vast IQVIA data and clinical trial resources to develop innovative, data-driven, and patient-centered solutions for Cardiovascular trials. The Medical Strategy Lead will provide senior clinical and scientific expertise to all IQVIA divisions as requested and will collaborate closely with indication-specific teams to develop integrated strategies for Cardiovascular clinical trials, mostly [. .. ] design/ clinical development plan, mining data to address important clinical questions relevant to the study, reviewing the protocol for scientific/ regulatory soundness and feasibility, identification of target site and principal investigator profiles, anticipated patient recruitment, standard of care and competitive landscape. Support preparation of customer and bid defense meetings, e. g. training and preparation of the assigned project team; provide specific content; ensure presentation focus and content effectively conveys Cardiovascular strategy. Attends and presents at customer meeting, or bid defense or [. .. ]
Job am 24.02.2026 bei Jobleads gefunden
• Frankfurt, Hesse
Führungs-/ Leitungspositionen
[. .. ] IQVIA CAGT portfolio through scientific and clinical expertise. The CAGT Medical Strategy Lead will be charged with using his/ her clinical, scientific, and operational knowledge to harness [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] the vast IQVIA data and clinical trial resources to develop innovative, data-driven, and patient-centered solutions for CAGT trials. The CAGT Medical Strategy Lead will provide clinical and scientific expertise to all IQVIA divisions as requested and will collaborate closely with indication-specific teams to develop integrated strategies for CAGT clinical trials and [. .. ] development plan, mining data to address important clinical questions relevant to the study, reviewing the protocol for scientific/ regulatory soundness and feasibility, logistics challenges, identification of target site and principal investigator profiles, anticipated patient recruitment, standard of care and competitive landscape. Support preparation of customer and bid defense meetings, e. g. training and preparation of the assigned project team; provide specific content; ensure presentation focus and content effectively conveys CAGT strategy. Attends and presents at customer meeting, or bid defense or [. .. ]
Job am 21.02.2026 bei Jobleads gefunden
Senior Medical Director-Cell and Gene Therapy (m/w/d)
• Frankfurt, Hesse
Führungs-/ Leitungspositionen
[. .. ] IQVIA CAGT portfolio through scientific and clinical expertise. The CAGT Medical Strategy Lead will be charged with using his/ her clinical, scientific, and operational knowledge to harness [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] the vast IQVIA data and clinical trial resources to develop innovative, data-driven, and patient-centered solutions for CAGT trials. The CAGT Medical Strategy Lead will provide clinical and scientific expertise to all IQVIA divisions as requested and will collaborate closely with indication-specific teams to develop integrated strategies for CAGT clinical trials and [. .. ] development plan, mining data to address important clinical questions relevant to the study, reviewing the protocol for scientific/ regulatory soundness and feasibility, logistics challenges, identification of target site and principal investigator profiles, anticipated patient recruitment, standard of care and competitive landscape. Support preparation of customer and bid defense meetings, e. g. training and preparation of the assigned project team; provide specific content; ensure presentation focus and content effectively conveys CAGT strategy. Attends and presents at customer meeting, or bid defense or [. .. ]
Job am 02.02.2026 bei Jobleads gefunden
Senior Director, Medical Strategic Lead-Psychiatrist
• Frankfurt, Hesse
Führungs-/ Leitungspositionen
[. .. ] the IQVIA CNS portfolio through scientific and clinical expertise. The Medical Strategy Lead will be charged with using his/ her clinical, scientific, and operational knowledge to harness [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] the vast IQVIA data and clinical trial resources to develop innovative, data-driven, and patient-centered solutions for CNS trials. The Medical Strategy Lead will provide senior clinical and scientific expertise to all IQVIA divisions as requested and will collaborate closely with indication-specific teams to develop integrated strategies for CNS clinical trials, mostly [. .. ] design/ clinical development plan, mining data to address important clinical questions relevant to the study, reviewing the protocol for scientific/ regulatory soundness and feasibility, identification of target site and principal investigator profiles, anticipated patient recruitment, standard of care and competitive landscape. Support preparation of customer and bid defense meetings, e. g. training and preparation of the assigned project team; provide specific content; ensure presentation focus and content effectively conveys CNS strategy. Attends and presents at customer meeting, or bid defense or [. .. ]
Job am 19.01.2026 bei Jobleads gefunden
Senior Director, Medical Strategy Lead-Cardiologist
• Wien
Führungs-/ Leitungspositionen
[. .. ] the IQVIA Cardiovascular portfolio through scientific and clinical expertise. The Medical Strategy Lead will be charged with using his/ her clinical, scientific, and operational knowledge to harness [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] the vast IQVIA data and clinical trial resources to develop innovative, data-driven, and patient-centered solutions for Cardiovascular trials. The Medical Strategy Lead will provide senior clinical and scientific expertise to all IQVIA divisions as requested and will collaborate closely with indication-specific teams to develop integrated strategies for Cardiovascular clinical trials, mostly [. .. ] design/ clinical development plan, mining data to address important clinical questions relevant to the study, reviewing the protocol for scientific/ regulatory soundness and feasibility, identification of target site and principal investigator profiles, anticipated patient recruitment, standard of care and competitive landscape. Support preparation of customer and bid defense meetings, e. g. training and preparation of the assigned project team; provide specific content; ensure presentation focus and content effectively conveys Cardiovascular strategy. Attends and presents at customer meeting, or bid defense or [. .. ]
Job am 15.01.2026 bei Jobleads gefunden
Senior/ Medical Director (Ophthalmology) 0.5 FTE
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, [. .. ]
Job am 13.01.2026 bei Jobleads gefunden
Senior Director, Medical Strategy Lead-Cardiologist
• Frankfurt, Hesse
Führungs-/ Leitungspositionen
[. .. ] new business targets; responsible for inclusion of cardiovascular elements into proposals. Provide scientific, clinical, and operational advice to internal stakeholders developing proposals: strategy to protocol design/ clinical [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] development plan, mining data, reviewing protocol for scientific/ regulatory soundness and feasibility, identification of target site and principal investigator profiles, anticipated patient recruitment, standard of care and competitive landscape. Support preparation of customer and bid defense meetings, training and preparation of the assigned project team; provide specific content; ensure presentation focus and content effectively conveys cardiovascular strategy; attend and present at customer meetings, bid defense or partnership meetings. Participate [. .. ]
Job am 23.11.2025 bei Jobleads gefunden
Medical Science Liaison Manager, Nephrology, South
• 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 [. .. ]
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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 136 offene Stellenanzeigen für Data Investigator Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Data Investigator Jobs?
Aktuell suchen 32 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:
- IQVIA (7 Jobs)
- GULP experts united (4 Jobs)
- PSI CRO (3 Jobs)
- Thermo Fisher Scientific (3 Jobs)
- Alexion Pharmaceuticals (3 Jobs)
- Dr. Falk Pharma GmbH (2 Jobs)
In welchen Bundesländern werden die meisten Data Investigator Jobs angeboten?
Die meisten Stellenanzeigen für Data Investigator Jobs werden derzeit in Bayern (22 Jobs), Baden-Württemberg (16 Jobs) und Hessen (11 Jobs) angeboten.
Zu welchem Berufsfeld gehören Data Investigator Jobs?
Data Investigator Jobs gehören zum Berufsfeld Datenbanken.
