212 Jobs für Data Investigator
Stellenangebote Data Investigator Jobs
Job vor 10 Tagen 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
Randstad Deutschland GmbH Co. KG
Elektrotechniker (m/w/d)
• Biberach an der Riß
Angebote von Zeitarbeitsunternehmen Abgeschlossenes Studium
Betriebliche Altersvorsorge Weihnachtsgeld 30+ Urlaubstage
Unsere Mission: Wir bringen Menschen zusammen Aktuell bietet unser Spezialistenteam von Randstad professional solutions eine attraktive Position als Techniker Elektrotechnik bzw. Process Expert
Data Integrity bei einem unserer Geschäftspartner aus [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] der Pharmabranche am Standort Biberach. Eine leistungsgerechte Entlohnung, persönliche Betreuung und gute Entwicklungsmöglichkeiten sind selbstverständlich. Wir freuen uns auf Sie Bewerben Sie sich jetzt direkt online Wir lieben Diversität und begrüßen daher jede Bewerbung Erfassung, Bewertung und Behebung von anlagenbedingten Störungen Identifizierung vorbeugender Maßnahmen [. .. ] elektronischer Daten Erarbeitung neuer Prozessabläufe unter Einhaltung von c GMP-Regularien Statistische Auswertung und Interpretation von Prozess- und Maschinenkenndaten Fungieren als Ansprechpartner bei technischen Fragen, Wartungen, Kalibrierungen und Projektarbeit Übernahme der Investigator-Rolle, inkl. Bearbeitung von Untersuchungen im Rahmen von Abweichungen, Leitung von Untersuchungen sowie Definition, Ausführung und Dokumentation von Maßnahmen zur Korrektur oder Vermeidung von Fehlern (CAPA) Aktive Teilnahme an Troubleshootings, inkl. Bewertung, Abstellen der Ursache und GMP-gerechte Dokumentation von Fehlfunktionen/ Störungen Übernahme der Rolle Change Manager bei der nachhaltigen [. .. ]
Job gestern bei Jooble gefunden
• Berlin
[. .. ] 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. The MSL will act as the medical representative across a large, complex environment with flexibility to support other countries as needed by the organisation. Responsibilities: Develop and maintain, in a self-driven manner, outstanding knowledge [. .. ] 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 Facilitate clear communication between the client and investigators in investigator engagement for both client trials and investigator-sponsored studies and barriers to enrolment for pipeline assets Works to the highest ethical compliance, ethics and safety standards adhering to all local regulations and laws Maintains [. .. ]
Job vor 2 Tagen bei Jooble gefunden
Sr CRA in oncology-Sponsor dedicated-Home Based Germany
• München
[. .. ] 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 via [. .. ]
Job vor 4 Tagen bei JobMESH gefunden
Thermo Fisher Scientific
• Baden- Wurttemberg
[. .. ] a site processes specialist, ensuring that the trial is conducted in accordance with the approved protocol, ICH-GCP guidelines, applicable regulations and SOPs to guarantee subjects rights, well-being [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and data reliability. Ensures audit readiness. Develops collaborative relationships with investigational sites. Detailed tasks and responsibilities assigned to role are outlined in the task matrix. Travel up to 50-75 A day in the Life: Monitors investigator sites with a risk-based monitoring approach applies root cause analysis (RCA) , critical thinking and problem-solving skills to identify site processes failure and corrective/ preventive actions to bring the site into compliance and decrease risks. Ensures data accuracy through SDR, SDV and CRF review as applicable through on-[. .. ]
Job vor 4 Tagen bei Jooble gefunden
Randstad Professional
Elektrotechniker (m/w/d) (Biberach an der Ri)
• Österreich
Angebote von Zeitarbeitsunternehmen Abgeschlossenes Studium
Betriebliche Altersvorsorge Weihnachtsgeld 30+ Urlaubstage
Unsere Mission: Wir bringen Menschen zusammen Aktuell bietet unser Spezialistenteam von Randstad professional solutions eine attraktive Position als Techniker Elektrotechnik bzw. Process Expert
Data Integrity bei einem unserer Geschftspartner aus [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] der Pharmabranche am Standort Biberach. Eine leistungsgerechte Entlohnung, persnliche Betreuung und gute Entwicklungsmglichkeiten sind selbstverstndlich. Wir freuen uns auf Sie Bewerben Sie sich jetzt direkt online Wir lieben Diversitt und begren daher jede Bewerbung Erfassung, Bewertung und Behebung von anlagenbedingten Strungen Identifizierung vorbeugender Manahmen [. .. ] elektronischer Daten Erarbeitung neuer Prozessablufe unter Einhaltung von c GMP-Regularien Statistische Auswertung und Interpretation von Prozess- und Maschinenkenndaten Fungieren als Ansprechpartner bei technischen Fragen, Wartungen, Kalibrierungen und Projektarbeit bernahme der Investigator-Rolle, inkl. Bearbeitung von Untersuchungen im Rahmen von Abweichungen, Leitung von Untersuchungen sowie Definition, Ausfhrungund Dokumentationvon Manahmen zur Korrektur oder Vermeidung von Fehlern (CAPA) Aktive Teilnahme an Troubleshootings, inkl. Bewertung, Abstellen der Ursache und GMP-gerechte Dokumentation von Fehlfunktionen/ Strungen bernahme der Rolle Change Manager bei der nachhaltigen Implementierung von [. .. ]
Job vor 5 Tagen bei Jooble gefunden
Abb Vie
• Wiesbaden
Work-Life-Balance
[. .. ] 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. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Ensures quality of data submitted from study sites and assures timely submission of data, including appropriate reporting and follow-up for all safety events by site personnel. Supports and/or conducts (accompanied) site qualification, initiation, interim monitoring and study closeout visits for Phase 1-4 studies in accordance with local regulations, Good Clinical Practices [. .. ] project team members. Supports with Clinical Trial Application submissions, including relevant informed consent local changes and translations into local language as required. Supports remote monitoring, if and as applicable. Negotiates investigator/ hospital agreements with stakeholders. Supports new and innovative processes and technologies to increase the quality, productivity, and efficiency of Clinical Operations and conserve overall departmental operating costs. Appropriate life-science or healthcare-related qualification or experience or equivalent work experience. One year of clinically-related experience in a medical profession, [. .. ]
Job vor 5 Tagen bei Jooble gefunden
Abb Vie
Clinical Study Specialist (Contract)
• Wiesbaden
Work-Life-Balance
[. .. ] 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. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Ensures quality of data submitted from study sites and assures timely submission of data, including appropriate reporting and follow-up for all safety events by site personnel. Supports and/or conducts (accompanied) site qualification, initiation, interim monitoring and study closeout visits for Phase 1-4 studies in accordance with local regulations, Good Clinical Practices [. .. ] project team members. Supports with Clinical Trial Application submissions, including relevant informed consent local changes and translations into local language as required. Supports remote monitoring, if and as applicable. Negotiates investigator/ hospital agreements with stakeholders. Supports new and innovative processes and technologies to increase the quality, productivity, and efficiency of Clinical Operations and conserve overall departmental operating costs. Appropriate life-science or healthcare-related qualification or experience or equivalent work experience. One year of clinically-related experience in a medical profession, [. .. ]
Job vor 5 Tagen bei Jooble gefunden
Abb Vie
• Wiesbaden
Work-Life-Balance
[. .. ] 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. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Ensures quality of data submitted from study sites and assures timely submission of data, including appropriate reporting and follow-up for all safety events by site personnel. Supports and/or conducts (accompanied) site qualification, initiation, interim monitoring and study closeout visits for Phase 1-4 studies in accordance with local regulations, Good Clinical Practices [. .. ] project team members. Supports with Clinical Trial Application submissions, including relevant informed consent local changes and translations into local language as required. Supports remote monitoring, if and as applicable. Negotiates investigator/ hospital agreements with stakeholders. Supports new and innovative processes and technologies to increase the quality, productivity, and efficiency of Clinical Operations and conserve overall departmental operating costs. Appropriate life-science or healthcare-related qualification or experience or equivalent work experience. One year of clinically-related experience in a medical profession, [. .. ]
Job vor 5 Tagen bei Jooble gefunden
Abb Vie
Clinical Senior Research Associate
• Wiesbaden
Work-Life-Balance
[. .. ] 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. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Ensures quality of data submitted from study sites and assures timely submission of data, including appropriate reporting and follow-up for all safety events by site personnel. Supports and/or conducts (accompanied) site qualification, initiation, interim monitoring and study closeout visits for Phase 1-4 studies in accordance with local regulations, Good Clinical Practices [. .. ] project team members. Supports with Clinical Trial Application submissions, including relevant informed consent local changes and translations into local language as required. Supports remote monitoring, if and as applicable. Negotiates investigator/ hospital agreements with stakeholders. Supports new and innovative processes and technologies to increase the quality, productivity, and efficiency of Clinical Operations and conserve overall departmental operating costs. Appropriate life-science or healthcare-related qualification or experience or equivalent work experience. One year of clinically-related experience in a medical profession, [. .. ]
Job vor 5 Tagen bei Jooble gefunden
Abb Vie
• Wiesbaden
Work-Life-Balance
[. .. ] 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. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Ensures quality of data submitted from study sites and assures timely submission of data, including appropriate reporting and follow-up for all safety events by site personnel. Supports and/or conducts (accompanied) site qualification, initiation, interim monitoring and study closeout visits for Phase 1-4 studies in accordance with local regulations, Good Clinical Practices [. .. ] project team members. Supports with Clinical Trial Application submissions, including relevant informed consent local changes and translations into local language as required. Supports remote monitoring, if and as applicable. Negotiates investigator/ hospital agreements with stakeholders. Supports new and innovative processes and technologies to increase the quality, productivity, and efficiency of Clinical Operations and conserve overall departmental operating costs. Appropriate life-science or healthcare-related qualification or experience or equivalent work experience. One year of clinically-related experience in a medical profession, [. .. ]
Job vor 6 Tagen bei Jooble gefunden
Abb Vie
Clinical Research Associate I
• Wiesbaden
Work-Life-Balance
[. .. ] activities as well as study conduct and site closure tasks. Manages the activities of clinical investigative sites across multiple protocols and multiple therapeutic areas, with appropriate supervision. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Ensures quality of data submitted from study sites and assures timely submission of data, including appropriate reporting and follow-up for all safety events by site personnel. Ensures safety and protection of study subjects. Supports and/or conducts (accompanied) site qualification, initiation, interim monitoring and study closeout visits for Phase 1-4 studies in [. .. ] as required. Supports remote monitoring, if and as applicable. Assists in study budget preparation and clinical study agreement execution, including ensuring necessary payments are made according to executed agreements. Negotiates investigator/ hospital agreements with stakeholders. Maintains and completes own expense reports as per local and applicable guidelines. Supports new and innovative processes and technologies to increase the quality, productivity, and efficiency of Clinical Operations and conserve overall departmental operating costs. Qualifications Appropriate life-science or healthcare-related qualification or experience or [. .. ]
Job vor 9 Tagen bei JobMESH gefunden
Thermo Fisher Scientific
• Baden- Wurttemberg Karlsruhe
[. .. ] perform remote site management and monitoring activities on assigned project (s) in accordance with FDA and/or local regulations and guidelines, ICH GCPs and company procedural documents by [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] reviewing study data from various sources remotely. You will contact study sites to collect study documentation, resolve issues and request outstanding information. A day in the Life: Develops and maintains a close and collaborative communication with the site staff. Actively discusses protocol conduction, enrollment rates and strategies, open issues, EDC completion and queries, [. .. ] specific guidelines. Raises manual queries in EDC when applicable. Remotely reviews study logs as deemed necessary. Conducts and documents site management calls/ contacts according to the monitoring plan. Participates in investigator meetings. Investigates and follows-up on centralized monitoring findings. Evaluates PI oversight (e. g. , protocol adherence) , subject safety and study processes to assess site s ability to conduct study on a regular basis. Conducts remote investigations into site performance using a risk based monitoring approach: applying root cause [. .. ]
Job vor 12 Tagen bei Jooble gefunden
Thermo Fisher Scientific
Clinical Trial Coordinator II (m/f/d) - Germany
• Karlsruhe
[. .. ] people and communities depend on now and in the future. Location/ Division Specific Information Our clinical department defines, develops and delivers clinical programmes. We ensure the highest-quality [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] review of data and effective interaction with study sites, including on-site monitoring throughout a study, ensuring that patients receive needed care, as well as identifying and treating clinical trial participants. Discover Impactful Work: PPD clinical research services mission is to improve health. It starts as an idea to cure. It becomes a [. .. ] We invite you to re-imagine health promoting protocols with us, working alongside our dedicated, forward-thinking and upbeat teams. A day in the Life: Performs PPD clinical research services investigator file reviews and logging of outstanding issues in project related tracking tools Reviews regulatory documents for proper content Liaises with monitor and investigative sites to resolve outstanding regulatory issues identified Disseminates study related information, including project tracking updates to Clients, clinical study teams and other PPD clinical research services departments [. .. ]
Job vor 13 Tagen bei Jooble gefunden
Helmholtz Association of German Research Centres
• Oldenburg
[. .. ] a hub for environmental and marine research. The institute brings together experts from 18 countries and provides state-of-the-art wet-lab and computational facilities. Generate and analyze genomic
MEHR INFOS ZUM STELLENANGEBOT
[...] class=highlight_text>data for reef-building corals, including eukaryotic genome assembly and annotation, population genomics, quantitative genetics, epigenetics, and gene expression analyses Use population genomic approaches to estimate population structure, history and introgression Use quantitative genetic approaches to estimate responses to selection model alternative conservation genetic strategies such as assisted gene flow and [. .. ] this reason, we established Career Development Centers for postdoctoral researchers in the Helmholtz Centers. This equips young researchers with the skills they need to go on to head a Helmholtz
Investigator Group, for example. As an Investigator Group leader, junior scientists can independently set up their own group to conduct research in their specialist field and acquire management skills. Within its talent management strategy, the Helmholtz Association pays special attention to the increased recruitment of talented female scientists both from Germany [. .. ]
▶ Zur Stellenanzeige
Job am 22.01.2026 bei Jooble gefunden
Helmholtz Association of German Research Centres
Postdoctoral Fellow (f/m/x) in Modeling AI in Neuro-Cognitive Aging 4068/ 2026/ 1
• Magdeburg
[. .. ] using parametric and non-parametric techniques, to characterize disease trajectories and deviations from healthy aging. Integrating Deep Learning approaches with Bayesian inference and latent variable models. Analyzing high-dimensional, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] multimodal data such as MRI, FLAIR, cognitive assessments, and fluid biomarkers. Contributing to high-impact scientific publications and presenting findings at international conferences. Collaborating closely within an interdisciplinary team across neuroscience, psychology, medicine, and data science. Mentoring junior researchers and supporting a constructive, collegial team culture. We welcome applications from researchers with [. .. ] this reason, we established Career Development Centers for postdoctoral researchers in the Helmholtz Centers. This equips young researchers with the skills they need to go on to head a Helmholtz Investigator Group, for example. As an Investigator Group leader, junior scientists can independently set up their own group to conduct research in their specialist field and acquire management skills. Within its talent management strategy, the Helmholtz Association pays special attention to the increased recruitment of talented female scientists both from Germany [. .. ]
Job am 21.01.2026 bei Jooble gefunden
Helmholtz Association of German Research Centres
• Deutschland
[. .. ] a world-leading, internationally oriented center for cutting edge research on neurodegenerative diseases. We are seeking a highly motivated and skilled Postdoctoral Researcher to develop new algorithms for [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] multi-omics data integration. Working at the intersection of data science and neuroepigenetics, our research aims to unravel the complex mechanisms underlying brain cell function and neurodegenerative diseases. The group is committed to fostering a collaborative and innovative research environment and works with large-scale imaging and sequencing datasets. We offer a 2-[. .. ] this reason, we established Career Development Centers for postdoctoral researchers in the Helmholtz Centers. This equips young researchers with the skills they need to go on to head a Helmholtz Investigator Group, for example. As an Investigator Group leader, junior scientists can independently set up their own group to conduct research in their specialist field and acquire management skills. Within its talent management strategy, the Helmholtz Association pays special attention to the increased recruitment of talented female scientists both from Germany [. .. ]
Job am 19.01.2026 bei Jooble gefunden
Lab Connect
Project Manager
• Köln
[. .. ] Functional Service Provider (FSP) Solutions, supporting our clients with scientific and technical expertise, acting as an extension of their team, coordinating all laboratory related needs, advising on [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] strategies for lab data collection and providing end-to-end analytical and logistical solutions. Job Summary The Project Manager is responsible for oversight of assigned clinical studies. The Project Manager will participate in development of Statements of Work (SOW) to define client expectations and will perform duties associated with day-to-day oversight of [. .. ] stored samples as directed in the SOW. Ensures that all laboratory requirements outlined in the protocol are managed per expectations and in compliance with laboratory practices. Creates training materials for investigator meetings as applicable. Represents Lab Connect at client and/or investigator meetings. Performs other related duties and tasks as necessary or as assigned. Education and Qualifications Scientific degree, preferably in a laboratory or life science, or equivalent combination of education and experience. Strongly preferred: Medical Technology or MLT/ MTL degree [. .. ]
Job am 17.01.2026 bei Jooble gefunden
Alira Health
• München
[. .. ] ICH GCP guidelines, and FDA regulations and within established timelines. Serves as study lead and primary contact for sponsors. Manages clinical study functions, which may include investigational [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] supply, IWRS/ IXRS, data management, biostatistics, pharmacovigilance, and central laboratory. Generates and presents frequent study status updates and reports to sponsor. Supervises and provides support to the Clinical team, including Clinical Assistants, In-house Clinical Research Associates, and Clinical Research Associates. Supervises and trains Associate PMs. Creates and reviews clinical study documents, including protocols, [. .. ] and communications to ensure timely attainment of trial milestones. Ensures accuracy of reports and material work product. Provides monthly billing information to finance team. Presents at project meetings such as investigator meetings and new client meetings. Updates management accurately and regularly through frequent communication. Identifies issues and develops problem-solving strategies to ensure study timelines are met. Manages subject accrual, retention, and compliance. Assists in TMF management and manages TMF reviews as needed. Prepares for and participates in third-party audits [. .. ]
Job am 17.01.2026 bei Jooble gefunden
Alira Health
Senior Project Director
• München
Führungs-/ Leitungspositionen
[. .. ] dont limit, but encourage, collaboration. The Project Manager (PM) is an important member of the Alira Health Clinical team. Manages clinical study functions, which may include investigational [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] supply, IWRS/ IXRS, data management, biostatistics, pharmacovigilance, and central laboratory. Supervises and provides support to the Clinical team, including Clinical Assistants, In-house Clinical Research Associates, and Clinical Research Associates. Creates and reviews clinical study documents, including protocols, ICF templates, study budgets, site log/ form templates, study manuals and plans, site binders, etc. Presents at project meetings such as investigator meetings and new client meetings. Updates management accurately and regularly through frequent communication. Manages subject accrual, retention, and compliance. Assists in TMF management and manages TMF reviews as needed. Complies with and ensures team compliance with ICH GCP guidelines, FDA regulations, and company SOPs. 3 years of experience in the [. .. ]
Job am 17.01.2026 bei Jooble gefunden
Alira Health
Senior Project Management Coordinator
• München
[. .. ] dont limit, but encourage, collaboration. The Project Manager (PM) is an important member of the Alira Health Clinical team. Manages clinical study functions, which may include investigational [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] supply, IWRS/ IXRS, data management, biostatistics, pharmacovigilance, and central laboratory. Supervises and provides support to the Clinical team, including Clinical Assistants, In-house Clinical Research Associates, and Clinical Research Associates. Creates and reviews clinical study documents, including protocols, ICF templates, study budgets, site log/ form templates, study manuals and plans, site binders, etc. Presents at project meetings such as investigator meetings and new client meetings. Updates management accurately and regularly through frequent communication. Manages subject accrual, retention, and compliance. Assists in TMF management and manages TMF reviews as needed. Complies with and ensures team compliance with ICH GCP guidelines, FDA regulations, and company SOPs. 3 years of experience in the [. .. ]
Job am 17.01.2026 bei Jooble gefunden
Alira Health
Senior Manager, Project Management
• München
[. .. ] dont limit, but encourage, collaboration. The Project Manager (PM) is an important member of the Alira Health Clinical team. Manages clinical study functions, which may include investigational [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] supply, IWRS/ IXRS, data management, biostatistics, pharmacovigilance, and central laboratory. Supervises and provides support to the Clinical team, including Clinical Assistants, In-house Clinical Research Associates, and Clinical Research Associates. Creates and reviews clinical study documents, including protocols, ICF templates, study budgets, site log/ form templates, study manuals and plans, site binders, etc. Presents at project meetings such as investigator meetings and new client meetings. Updates management accurately and regularly through frequent communication. Manages subject accrual, retention, and compliance. Assists in TMF management and manages TMF reviews as needed. Complies with and ensures team compliance with ICH GCP guidelines, FDA regulations, and company SOPs. 3 years of experience in the [. .. ]
Job am 17.01.2026 bei Jooble gefunden
Alira Health
Project Manager Senior
• München
[. .. ] dont limit, but encourage, collaboration. The Project Manager (PM) is an important member of the Alira Health Clinical team. Manages clinical study functions, which may include investigational [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] supply, IWRS/ IXRS, data management, biostatistics, pharmacovigilance, and central laboratory. Supervises and provides support to the Clinical team, including Clinical Assistants, In-house Clinical Research Associates, and Clinical Research Associates. Creates and reviews clinical study documents, including protocols, ICF templates, study budgets, site log/ form templates, study manuals and plans, site binders, etc. Presents at project meetings such as investigator meetings and new client meetings. Updates management accurately and regularly through frequent communication. Manages subject accrual, retention, and compliance. Assists in TMF management and manages TMF reviews as needed. Complies with and ensures team compliance with ICH GCP guidelines, FDA regulations, and company SOPs. 3 years of experience in the [. .. ]
Job am 17.01.2026 bei Jooble gefunden
Alira Health
Senior Project Management Officer
• München
[. .. ] dont limit, but encourage, collaboration. The Project Manager (PM) is an important member of the Alira Health Clinical team. Manages clinical study functions, which may include investigational [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] supply, IWRS/ IXRS, data management, biostatistics, pharmacovigilance, and central laboratory. Supervises and provides support to the Clinical team, including Clinical Assistants, In-house Clinical Research Associates, and Clinical Research Associates. Creates and reviews clinical study documents, including protocols, ICF templates, study budgets, site log/ form templates, study manuals and plans, site binders, etc. Presents at project meetings such as investigator meetings and new client meetings. Updates management accurately and regularly through frequent communication. Manages subject accrual, retention, and compliance. Assists in TMF management and manages TMF reviews as needed. Complies with and ensures team compliance with ICH GCP guidelines, FDA regulations, and company SOPs. 3 years of experience in the [. .. ]
Job am 16.01.2026 bei Jooble gefunden
Helmholtz Association of German Research Centres
Postdoctoral Researcher (f/m/x) in Predictive Avifauna Modelling
• Leipzig
[. .. ] join a team at its inception that will define the future of predictive biodiversity conservation science in Europe. The project will be fueled by fine-scale, high-resolution bird [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] monitoring data from key partners like the Dachverband Deutscher Avifaunisten (DDA) , which must be harmonized with broader, continental-scale environmental data streams (e. g. , climate projections, remote sensing land cover) . Success in this role will require not just technical skill, but a deep appreciation for spatial ecology and the [. .. ] this reason, we established Career Development Centers for postdoctoral researchers in the Helmholtz Centers. This equips young researchers with the skills they need to go on to head a Helmholtz Investigator Group, for example. As an Investigator Group leader, junior scientists can independently set up their own group to conduct research in their specialist field and acquire management skills. To this end, there are currently two funding programs supporting this policy: and Helmholtz Distinguished Professorship Funding for the recruitment of leading [. .. ]
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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 212 offene Stellenanzeigen für Data Investigator Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Data Investigator Jobs?
Aktuell suchen 35 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:
- Helmholtz Association of German Research Centres (29 Jobs)
- Thermo Fisher Scientific (10 Jobs)
- Abb Vie (6 Jobs)
- Alira Health (6 Jobs)
- Incyte Corporation (5 Jobs)
- IQVIA (5 Jobs)
In welchen Bundesländern werden die meisten Data Investigator Jobs angeboten?
Die meisten Stellenanzeigen für Data Investigator Jobs werden derzeit in Bayern (24 Jobs), Nordrhein-Westfalen (12 Jobs) und Hessen (10 Jobs) angeboten.
Zu welchem Berufsfeld gehören Data Investigator Jobs?
Data Investigator Jobs gehören zum Berufsfeld Datenbanken.
