124 Jobs für Compliance Investigator
Stellenangebote Compliance Investigator Jobs
Job vor 4 Tagen bei Aktuelle TopJobs gefunden
Deutsche Rentenversicherung Baden- Württemberg
Sachbearbeiter/in Projektbüro (m/w/d)
• Karlsruhe oder Stuttgart
Sachbearbeiter/in Projektbüro (m/w/d) Deutsche Rentenversicherung Baden-Württemberg Karlsruhe oder Stuttgart Die Deutsche Rentenversicherung (DRV) Baden Württemberg ist einer der größten Regionalträger der gesetzlichen Rentenversicherung mit rund 3.600 Mitarbeitenden. Unsere Digitalisierungsabteilung stellt [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Anwenderinnen und Anwendern ein breit [. .. ]
Neu Job vor 4 Std. bei Mindmatch.ai gefunden
Syneos Health, Inc.
On-site monitor open to diverse EMEA countries
• AT- 9 Wien
Job Responsibilities Perform site management activities in
compliance with Company and Sponsor Standard Operating Procedures (SOPs) and Work Instructions (WIs) . Assure compliance with local regulations and appropriate guidance for [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] assigned study design/ classification, including Good Pharmacoepidemiology Practices (GPP) and International Conference on Harmonisation Good Clinical Practice (ICHGCP) . Conduct site management activities as per agreed Scope of [. .. ] sites for assigned studies. Site startup with minimal supervision, working with study startup and regulatory teams. Conduct all remote and onsite monitoring activities through all study stages. Routinely review the Investigator Site File (ISF) for accuracy, timeliness and completeness; reconcile its contents with the Trial Master File (TMF) ; and ensure sites archive essential documents per local guidelines. Document activities via confirmation letters, followup letters, trip reports, communication logs, and other required project documents per SOPs and SMP; support subject recruitment, [. .. ]
Job vor 6 Tagen bei Mindmatch.ai gefunden
IQVIA
• AT- 9 Wien
[. .. ] delivering industryleading outcomes. Location: Vienna, Austria (Office based) Job Overview As a Site Activation Administrative Coordinator, under general supervision, you will perform countrylevel tasks associated with site [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] activation activities, ensuring compliance with local and international regulations, SOPs, project requirements and contractual/ budgetary guidelines. You will review documents for completeness, consistency and accuracy, prepare site regulatory documents, track progress, approve and execute regulatory, ethics, informed consent, and investigator pack release documents, and distribute completed documents to sites and internal project team members. Additionally, you will support the maintenance of internal systems, databases, tracking tools, timelines and project plans with accurate, projectspecific information. Requirements Bachelors Degree Good interpersonal, communication and organisational skills to establish and maintain effective working relationships [. .. ]
Job vor 7 Tagen bei Mindmatch.ai gefunden
Chain Scale
Crypto Market Abuse Investigator Surveillance
• AT- 9 Wien
[. .. ] markets. This role requires strong analytical capabilities and a background in market abuse, surveillance, or financial crime monitoring. Responsibilities include monitoring trading activities for signs of insider [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] dealing and supporting compliance with regulatory frameworks. Successful candidates will have 37+ years of relevant experience, preferably in regulated financial markets. J-18808-Ljbffr 90433529 [. .. ]
Job vor 8 Tagen bei Mindmatch.ai gefunden
EM Tensor GmbH
• AT- 9 Wien
[. .. ] with complex hardware-software systems; ability to translate technical imaging requirements into structured experimental protocols Independent, reliable, and quality-focused working style with strong attention to detail specificallyregardingmeasurement accuracy, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] calibration compliance, and technical documentation (Validation Verification) Comfortable following andmaintaining SOPs in a regulated medical device environment (ISO 13485/ EU MDR context) Good command of English, written and spoken, is essential; German is notrequired Technical Skills Required Experience with Vector Network Analyzers (VNA) : S-parameter measurement, calibration, data export Familiarity with RF [. .. ] design choices, inclusionpositioning, and interpretation of anomalous scan results. Familiarity with clinical investigation concepts: informed consent, inclusion/ exclusion criteria, adverse event reporting, source data, and the role of sponsor vs. investigator. The Test Engineer will interact with clinical data workflows and must understand the regulatory context of the measurements they produce. Key Responsibilities Daily Calibration and Environmental Monitoring Execute the daily system calibration before each scanning session: empty field scan, automated S-parameter comparison against reference values, and verification of dual [. .. ]
Job am 18.04.2026 bei Mindmatch.ai gefunden
Bitget
Senior KYT Investigator Crypto Compliance AML
• AT- 9 Wien
A leading digital assets ecosystem in Vienna is seeking an experienced AML
Investigator to conduct thorough investigations and manage transaction monitoring. The ideal candidate will have over 5 years of [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] experience in AML/ AFC and strong exposure to crypto transaction monitoring. Responsibilities include performing KYT investigations and supporting compliance efforts while leveraging blockchain analytics tools. Excellent communication skills in English are essential, with German being a plus. J-18808-Ljbffr 88999150 [. .. ]
Job am 01.04.2026 bei Mindmatch.ai gefunden
Abb Vie
• AT- 9 Wien
[. .. ] level project management to medical activities, that include evidence generation, planning processes, and management of Quality System documentation. Participates and supports in medical operations responsibilities related to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] non-interventional studies, investigator-initiated-studies, collaborative research studies ensuring compliance with local laws, guidelines and Abb Vies internal requirements, interacts with Global, Area and local medical team regarding issues, timelines, resources and general activities. Builds up competence and support for medical affairs teams in strategic and innovative primary secondary evidence generation (RWE) studies and projects (e. g. HTA) . Ensures [. .. ]
Job am 30.03.2026 bei Mindmatch.ai gefunden
Allergan
Affiliate Medical Operations Advisor (1 year contract, m/w/d)
• AT- 9 Wien
[. .. ] to medical activities, that include evidence generation, planning processes, and management of Quality System documentation. Core Job Responsibilities Participates and supports in medical operations responsibilities related to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] non-interventional studies, investigator-initiated-studies, collaborative research studies ensuring compliance with local laws, guidelines and Abb Vies internal requirements, interacts with Global, Area and local medical team regarding issues, timelines, resources and general activities. Builds up competence and support for medical affairs teams in strategic and innovative primary secondary evidence generation (RWE) studies and projects (e. g. HTA) . Ensures [. .. ]
Job am 11.03.2026 bei Mindmatch.ai gefunden
Teleflex
• AT- 9 Wien
Expected Travel: More than 50 Requisition ID: 13617 Position Summary The Clinical Research Associate (CRA) is responsible for scheduling and conducting on-site and remote monitoring visits in
compliance with [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] applicable regulatory standards (MDR, ISO 14155, ICH/ GCP guidelines, Teleflex procedures and IRB/ EC policies) . The CRA conducts monitoring visits as identified by the monitoring plan, study team or department needs to evaluate data accuracy and subject safety required by review of regulatory documents, medical records, reported data [. .. ] visit preparation. Conducts monitoring visits per the department SOP, WIs and monitoring plans. Applies MDR, ISO 14155, ICH/ GCP guidelines and Teleflex SOP and WIs to monitoring activities. Completes the Investigator Files with all appropriate documentation. Ensures all required documentation is completed prior to site initiation, during enrollment and followup, and at site close out. Provides findings to site staff, clear directions for resolution, appropriate retraining, and reviews data queries with site staff to ensure they are understood and can be [. .. ]
Job am 06.03.2026 bei Mindmatch.ai gefunden
Alimentiv
Join our Talent Pool-Clinical Research Associates (Eastern Europe)
• AT- 9 Wien
[. .. ] with the team About the Role (s) Clinical Research Associate I/ II Support/ conduct (as appropriate) site management through remote and supervised onsite visits (initiation, monitoring, and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] close-out) in compliance with SOPs, protocol, and GCP. 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 25.02.2026 bei Mindmatch.ai gefunden
IQVIA
• AT- 9 Wien
Essential Functions Develop coordinate the development of
investigator grants and estimates, contracting strategies and proposal text to support the proposal development process. Develop contract language, payment language and budget [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] templates as required as applicable to the position. Utilize and maintain contracting systems, tools, processes, and training materials for selected sponsors, studies or multi-protocol programs according to the [. .. ] within the agreed project strategy. Ensure collaboration, including communication with sponsors, stakeholders and RSU regions and countries as applicable to the position, to successfully deliver the agreed project scope in compliance with sponsor requirements and/or the RSU Management Plan. Provide specialist legal, operational and financial contracting support to the Study Teams, as applicable to site agreements to facilitate efficient business development and initiation and maintenance of clinical trials, whilst enabling compliance with regulatory requirements. Ensure overall contracting efficiency and adherence [. .. ]
Job am 22.02.2026 bei Mindmatch.ai gefunden
Job Squad
German-speaking Customer Service for Netflix Athens (Remote in Greece)
• AT- 9 Wien
[. .. ] and complete information by using the proper procedures Build a meaningful relationship, answering customers questions in a courteous, friendly, and professional manner Meet and exceed our customer [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] service quality goals, compliance regulations, and productivity targets Create a great customer experience that people value and we are proud of Be responsible for following the direction of the management and providing feedback Your qualifications: You speak and write German at a native level and you are fluent in English (B2) . Experience in [. .. ] but not a must. You have a basic understanding and level of computer handling skills. Excellent multitasking skills. You have a desire to learn and advance, and be a curious investigator and problem solver. Strong communication skills with excellent phone conversation skills, attentive listening skills. You have good interpersonal relationship building skills. If you have any questions about the position, please feel free to send an email to Our recruiters are ready to help J-18808-Ljbffr 81494411 [. .. ]
Job am 17.04.2026 bei Jobleads gefunden
• Eschborn, Hessen
Führungs-/ Leitungspositionen
[. .. ] product safety processes and procedures for new products and technologies as clinical studies are implemented, worldwide regulatory approvals are obtained and new products are commercialized. Key responsibilities [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Regionally responsible for Investigator Initiated Study and Research Grant programs Develop the priorities for the Global Abbott HF ISS strategy Responsible for medical affairs contributions to physician level professional education on advanced HF, MCS and hemodynamic management Work with professional societies on increasing awareness and knowledge about advanced HF and hemodynamic management Assists the [. .. ]
Job am 08.04.2026 bei Jobleads gefunden
Sr. Medical Affairs Manager-DACH (w, m, d)
[. .. ] training with generation and delivery of medical content Inform strategize evidence generation plans, in answer to fulfil market access, regulatory and marketing needs Support the local execution [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] of Insuletsponsored and Investigator Initiated trials Disseminate evidence within local markets Identify and engage with HCP to inform and seek advice on the companys solutions, through the execution of advisory boards, clinical activity, scientific Exchange and educational Events Establish and maintain credible peertopeer scientific relationships with national and regional KOLs Build confidence and advocacy [. .. ]
Job am 08.04.2026 bei Jobleads gefunden
• Berlin
Jobticket
[. .. ] or lung cancer. Support clinical trials by identifying study sites, participating in SIVs (Site Initiation Visits) , assisting with patient enrollment, and ensuring smooth information exchange. Identify [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] research opportunities, including Investigator Initiated Trials, Real World Evidence, and other evidencegeneration studies. Represent the organization at scientific conferences, advisory boards, and educational events, sharing insights and preparing reports for internal stakeholders. Ensure timely documentation of HCP interactions, compliance with local policies, and accurate reporting of insights and safety information. A Good Match: Advanced degree (Ph D, MD, or Pharmacist) with at least 5 years of experience in Medical Science Liaison (MSL) or Medical Affairs roles in Germany. Minimum 3 years of experience and an established network in Breast Cancer [. .. ]
Job am 06.04.2026 bei Jobleads gefunden
Medical Affairs Director Kardiologie (m/w/d) Wohnort bundesweit
• Frankfurt, Hesse
Führungs-/ Leitungspositionen Homeoffice möglich
[. .. ] klinischen Studien und Daten sowie deren Auswirkung auf die medizinische Kommunikations- und Studienstrategie Erstellung, Prüfung und Freigabe medizinisch-wissenschaftlicher Inhalte (z. B. Broschüren, Präsentationen, Trainingsunterlagen) Planung, Vorbereitung und [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Koordination von Investigator-initiated Trials (IITs) und Sammlung klinischer Daten Beobachtung und Bewertung aktueller wissenschaftlicher Entwicklungen, Leitlinien und klinischer Trends im Bereich Kardiologie Ihr Profil: Abgeschlossenes naturwissenschaftliches oder medizinisches Studium (z. B. Medizin, Pharmazie, Biowissenschaften) Mehrjährige Berufserfahrung im Bereich Medical Affairs, idealerweise in der Medizintechnik bevorzugt in der Kardiologie (structural heart) Erfahrung in [. .. ]
Job am 04.04.2026 bei Jobleads gefunden
• München, Bayern
[. .. ] and per GCP guidelines Advise clients, project teams, sites, regulatory agencies and third-party vendors on medical matters Collaborate with internal departments in the preparation of clinical development [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] plans, protocols, investigator brochures, annual reports, clinical study reports, patient narratives, and scientific presentations Review and analysis of clinical data to ensure the safety of study participants in clinical trials Ensure that the reported trial data is accurate, complete, and verifiable, and that the conduct of the trial is in compliance with the currently approved protocol/ amendments Address safety issues across the trial from sites and the study team Provide support for medical data review Participate in bid defense meetings and proposal activities Assist in Pharmacovigilance activities Identify trial risks, and create and implement mitigation strategies with other relevant departments Organize [. .. ]
Neu Job vor 4 Std. bei Jooble gefunden
GSK
Heme Clinical Trial RMAM (m/f/d)
• Deutschland Deutschland, DE
[. .. ] area for the role. Excellent verbal and written communication skills in German and English. Willingness and ability to travel regularly within the assigned region. Solid understanding of [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] regulatory, ethical and compliance requirements in the pharmaceutical environment. Preferred Qualification If you have the following characteristics, it would be a plus: Prior experience in oncology, hematology or related therapy areas. Experience supporting investigator-initiated trials or clinical partnerships. Experience designing or delivering omnichannel engagement plans and digital medical communications. Project management or budget management experience. Experience presenting at national or regional scientific meetings. A collaborative mindset and commitment to inclusive working with diverse stakeholders. Weitere Informationen: #EBDE #LI-Vii V #LI-[. .. ]
Job vor 2 Tagen bei Jooble gefunden
• Region München, Bayern; Regierungsbezirk Oberbayern; Bayern
[. .. ] Performs site qualification, site initiation, interim monitoring, site management and close-out visits (performed on-site or remotely) ensuring regulatory, ICH-GCP and/or Good Pharmacoepidemiology Practice (GPP) and protocol
MEHR INFOS ZUM STELLENANGEBOT
[...] class=highlight_text>compliance. Uses judgment and experience to evaluate overall performance of site and site staff and to provide recommendations regarding site-specific actions; immediately communicates/ escalates serious issues to the project team and develops action plans. Maintains a working knowledge of ICH/ GCP Guidelines or other applicable guidance, relevant regulations, and company [. .. ] each subject/ patient as required/appropriate. Demonstrates diligence in protecting the confidentiality of each subject/ patient. Assesses factors that might affect subject/ patients safety 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 [. .. ]
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Job vor 2 Tagen bei Jooble gefunden
Foundever
German Advisor for a Global Fintech Company-Larnaca
• Ausland Ausland, DE
[. .. ] Offer specialized customer support through written and phone communication Build meaningful relationship, answering customers questions in a courteous, friendly, and professional manner Meet and exceed our customer [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] service quality goals, compliance regulations and productivity targets Create amazing customer experience that people value and we are proud of Be responsible to follow the direction of management and provide feedback To succeed in the role, you will need to have: Native or proficient level of German (C2) Intermediate level of English (B1) Strong [. .. ] skills with excellent phone conversation skills, attentive listening and superior writing skills Analytical and problem solving skills with strong attention to detail Desire to learn and advance, be a curious investigator and problem solver Must hold EU citizenship or valid work permit for Cyprus Be a local candidate or willing to relocate to Larnaca, Cyprus (work on site) Benefits. Company-provided housing in Larnaca and round-trip flight covered Competitive fixed monthly salary plus an attractive, uncapped commission system Paid professional [. .. ]
Job vor 2 Tagen bei Jooble gefunden
Foundever
German Customer Advisor for NIKON-Lisbon, Portugal
• Ausland Ausland, DE
[. .. ] customers demands by identifying and troubleshooting with the available resources Build meaningful relationship, answering customers questions in a courteous, friendly, and professional manner Meet and exceed our [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] service quality goals, compliance regulations and productivity targets Create amazing experience that people value and we are proud of Be responsible to follow the direction of management and provide feedback To succeed in the role, you will need to have: Native or proficient level of German (C2) Advanced level of English (at least C1) [. .. ] skills with excellent phone conversation skills, attentive listening and superior writing skills Analytical and problem solving skills with strong attention to detail Desire to learn and advance, be a curious investigator and problem solver High-speed internet access and appropriate conditions for remote work Must hold EU citizenship or valid work permit for Portugal Be a local candidate or willing to relocate to sunny Lisbon, Portugal Benefits. Relocation package Competitive wages Paid professional training Employee discounts Private healthcare dental insurance (after [. .. ]
Job vor 3 Tagen bei Jooble gefunden
Colgate- Palmolive Company
Scientific Affairs Manager (f/m/d)
• Hamburg
[. .. ] Agrees allocation of educational events and target external speakers (Mid-level influencers) to be managed by the Education Managers in alignment with local POC manager and/or PBM; monitors [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] success, compliance and adjusts professional education framework in alignment with HUB priorities. Adapts and deploys professional/ scientific master initiatives materials on technologies brands via Education Managers, as part of local professional brand support plans and in line with business priorities; Facilitates investigator-initiated clinical research proposals through approval, contracting, completion, presentation, and publication, in alignment with EU Division agreed policy on IIT. Maintains relevant information in the company databases while securing legal and ethical compliance of the established interactions. Provides support to all Marketing functions and Customer Development for localization, implementation and [. .. ]
Job vor 3 Tagen bei Jooble gefunden
Biontech
Associate Director Audit Management
• Regierungsbezirk Rheinhessen- Pfalz; Rheinland- Pfalz Mainz, DE
Führungs-/ Leitungspositionen
As Associate Director Audit Management, you will play a pivotal role in ensuring the quality and
compliance of Bio NTechs clinical trials and processes. As part of the Global [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Development Quality Assurance team, you will lead audits across Good Clinical Practice (GCP) , Good Laboratory Practices (GLP) , Good Pharmacovigilance Practice (GVP) , and Information Technology (IT) domains. Your work will directly contribute to advancing Bio NTechs mission by ensuring adherence to regulatory standards and fostering continuous improvement in clinical development activities. Your Contribution: Lead global audits with a focus on clinical investigator sites and vendor audits in the EU, UK, and surrounding regions Ensure audit objectives align with risk-based strategies to uphold quality standards Coordinate and oversee audits conducted by contracted auditors, including scheduling, resource selection, and report reviews Execute audits as the lead auditor for non-contracted audits (remote or [. .. ]
Job vor 4 Tagen bei Jooble gefunden
Indero
Project Manager II (Germany)
• Unstrut- Hainich- Kreis; Thüringen Thueringen
[. .. ] II has the overall responsibility for the successful initiation, planning, execution, monitoring, controlling and closure of assigned clinical trials. The project manager II oversees and coordinates study [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] resources to ensure compliance with the study budget, project scope and timelines and in accordance with applicable standard operating procedures (SOPs) , good clinical practices, regulatory and study-specific requirements. Project Manager II acts as the main line of communication to relevant stakeholders and provides input to feasibility, study design, budget development and ensures [. .. ] such as; study plans, protocol, informed consent form, electronic case report form (e CRF) , tables/ listings/ figures (TLFs) , clinical study report. Participate in the planning and conduct of the Investigator s Meeting. Ensure that each site has the necessary material to adequately perform the study (e. g. , investigational product, study supplies, special equipment, safety lab kits, etc. ) . Lead study start-up activities including trial kick-off, TMF setup, site selection and activation, vendor set-up timelines, and [. .. ]
Job vor 4 Tagen bei Jooble gefunden
Foundever
German Sales Advisor for Financial Software Company-Porto
• Ausland Ausland, DE
[. .. ] the process of Sale Solve with precision and efficiency emerging issues that customers may face Perform corrections and optimize the customers technical knowledge Meet and exceed our [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] service quality goals, compliance regulations and productivity targets Create amazing experience that people value and we are proud of Be responsible to follow the direction of management and provide feedback To succeed in the role, you will need to have: Native or proficient level of German (C2) Advanced level of English (at least C1) [. .. ] skills with excellent phone conversation skills, attentive listening and superior writing skills Analytical and problem solving skills with strong attention to detail Desire to learn and advance, be a curious investigator and problem solver Must hold EU citizenship or valid work permit for Portugal Be a local candidate or willing to relocate to Porto, Portugal Benefits. Signing bonus Relocation package Competitive wages Paid professional training Employee discounts Private healthcare dental insurance (after six months of employment) Growth opportunities through various development [. .. ]
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Häufig gestellte Fragen
Wieviel verdient man als Compliance Investigator pro Jahr?
Als Compliance Investigator verdient man zwischen EUR 50.000,- bis EUR 80.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Compliance Investigator Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 124 offene Stellenanzeigen für Compliance Investigator Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Compliance Investigator Jobs?
Aktuell suchen 26 Unternehmen nach Bewerbern für Compliance Investigator Jobs.
Welche Unternehmen suchen nach Bewerbern für Compliance Investigator Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Compliance Investigator Stellenangebote:
- Biontech (6 Jobs)
- Foundever (4 Jobs)
- Thermo Fisher Scientific (4 Jobs)
- IQVIA (2 Jobs)
- Incyte Corporation (2 Jobs)
- Chronos Consulting (2 Jobs)
In welchen Bundesländern werden die meisten Compliance Investigator Jobs angeboten?
Die meisten Stellenanzeigen für Compliance Investigator Jobs werden derzeit in Bayern (35 Jobs), Nordrhein-Westfalen (13 Jobs) und Rheinland-Pfalz (7 Jobs) angeboten.
Zu welchem Berufsfeld gehören Compliance Investigator Jobs?
Compliance Investigator Jobs gehören zum Berufsfeld Compliance & Datenschutz.
