23 Jobs für Security Investigator
Stellenangebote Security Investigator Jobs
Job vor 3 Tagen bei Jobleads gefunden
• Wien
Führungs-/ Leitungspositionen Abgeschlossenes Studium
Varied tasks
Security and stability Comprehensive training Modern Office Unser Auftraggeber, Almirall Gmb H, ist ein globales biopharmazeutisches Unternehmen mit Schwerpunkt auf medizinische Dermatologie, das mit innovativen Therapien die Hautgesundheit [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] verbessert. Mit einer sehr guten Produktpipeline und starker Forschung und Entwicklung verbindet unser Kunde wissenschaftliche Exzellenz mit marktnaher Umsetzung und nachhaltigem Wachstum. Wir wenden [. .. ] Sicherstellung, dass alle Leistungen unter Einhaltung aller geltenden Qualitätsprozesse, externen Anforderungen, ethischen Standards und geschäftlichen Anforderungen erbracht werden Koordination von Real-World Evidence (RWE) Projekten sowie Identifikation und Begleitung von Investigator-Initiated Studies (IIS) Review und Freigabe (promotionaler) Materialien Ihr Profil Abgeschlossenes Studium der Human-oder Veterinärmedizin, Pharmazie oder einer naturwissenschaftlichen Disziplin (MSc, MD, Ph D) Einschlägige Medical-Affairs-Erfahrung in einem Pharmaunternehmen, Expertise im Bereich Dermatologie wünschenswert, aber nicht Voraussetzung Erfahrung in der Zusammenarbeit mit Commercial-/ Marketing-Funktionen sowie Verständnis für [. .. ]
Job vor 7 Tagen bei Jobleads gefunden
Quality Assurance Officer New Belgium
Are you interested in working directly for a single sponsor while having the
security and additional career opportunities that working for a global CRO can bring? Our team says its [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] the best of both worlds. Clin Choice is searching for a Quality Assurance Officer to work with one of our partner healthcare companies. This is a full-time (1FTE) position for 12months and we [. .. ] Goods reporting and management. Local Complaint Coordinator. Local Documentation Coordinator, including coordinate implementation at local level of corporate documentation, author and publish SOPs, and SOP periodic review. NCR/ CAPA initiator, investigator or task assignee (as needed) . Support implementation of Field Action. Support training planning and carry out reporting. Support the maintenance and management of the document retention system. Participate in Regulatory Affairs activities as needed. Education, Experience and Skills: Bachelors or Masters degree in a relevant scientific discipline. Prior experience [. .. ]
Job vor 7 Tagen bei Jobleads gefunden
• München, Bayern
Beratungs-/ Consultingtätigkeiten
[. .. ] 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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. [. .. ] the effective conduct of the clinical study data review and capture. Verifies site compliance with electronic data capture requirements. May perform investigational product (IP) inventory, reconciliation and reviews storage and security. Verifies the IP has been dispensed and administered to subjects/ patients according to the protocol. Verifies issues or risks associated with blinded or randomized information related to IP. Applies knowledge of GCP/ local regulations and organizational procedures to ensure IP is appropriately (re) labelled, imported and released/returned. Routinely reviews [. .. ]
Job vor 10 Tagen bei Jobleads gefunden
CRA Germany or Austria-single-client
• München, Bayern
Beratungs-/ Consultingtätigkeiten
[. .. ] 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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. [. .. ] the effective conduct of the clinical study data review and capture. Verifies site compliance with electronic data capture requirements. May perform investigational product (IP) inventory, reconciliation and reviews storage and security. Verifies the IP has been dispensed and administered to subjects/ patients according to the protocol. Verifies issues or risks associated with blinded or randomized information related to IP. Applies knowledge of GCP/ local regulations and organizational procedures to ensure IP is appropriately (re) labelled, imported and released/returned. Routinely reviews [. .. ]
Job vor 13 Tagen bei Jobleads gefunden
• Essen, Nordrhein- Westfalen
[. .. ] the applicable Standard Operating Procedures (SOPs) and the applicable laws and regulations. He/ she is the primary responsible person for communication on operational study related activities between [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] the Sponsor, the Investigator and other study personnel to build and maintain successful working relationships. The most important responsibility is to ensure that the subjects rights are respected and that all collected clinical trial data are accurate, complete, and verifiable from source documents. Main Responsibilities Acknowledges, follows ensures compliance with the Companys Quality and Information Security Management Systems, ICH GCP guidelines, applicable local and international legislation, including data protection legislation, as well as any amendments or updates the above In case of deviation from the approved protocol, ICH GCP guidelines and/or applicable legislation during the study conduct, the CRA is responsible for reporting it to [. .. ]
Job vor 13 Tagen bei Jobleads gefunden
Clinical Research Associate
• Düsseldorf, Nordrhein- Westfalen
[. .. ] the applicable Standard Operating Procedures (SOPs) and the applicable laws and regulations. He/ she is the primary responsible person for communication on operational study related activities between [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] the Sponsor, the Investigator and other study personnel to build and maintain successful working relationships. The most important responsibility is to ensure that the subjects rights are respected and that all collected clinical trial data are accurate, complete, and verifiable from source documents. Main Responsibilities Acknowledges, follows ensures compliance with the Companys Quality and Information Security Management Systems, ICH GCP guidelines, applicable local and international legislation, including data protection legislation, as well as any amendments or updates the above In case of deviation from the approved protocol, ICH GCP guidelines and/or applicable legislation during the study conduct, the CRA is responsible for reporting it to [. .. ]
Job am 05.12.2025 bei Jobleads gefunden
• Hamburg
Overview Job Description :
SECURITY CLEARANCE : Eligibility to gain UK SC Security Clearance TRAVEL REQUIRED : Some LOCATION : Filton, Site (60 of your working week must be [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] office based) TYPE : Full time Whats in it for you Financial Reward : Competitive salary, annual profit share, contributory pension, share options, car leasing scheme, [. .. ] research create real-world impact and collaborate with leading experts inside and outside of Airbus, this is the perfect position for you. How you will contribute to the team Scientific Investigator : Youll be at the forefront of your field, conducting scientific research and staying current with the state-of-the-art (Sot A) . This means not just following research, but actively contributing to it. Technology Developer : You are responsible for creating new techno bricks, which are building blocks for [. .. ]
Job am 21.11.2025 bei Jobleads gefunden
Clinical Research Associate
• Darmstadt, Hessen
Homeoffice möglich
[. .. ] the applicable Standard Operating Procedures (SOPs) and the applicable laws and regulations. He/ she is the primary responsible person for communication on operational study related activities between [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] the Sponsor, the Investigator and other study personnel to build and maintain successful working relationships. The most important responsibility is to ensure that the subjects rights are respected and that all collected clinical trial data are accurate, complete, and verifiable from source documents. Main responsibilities:-Acknowledges, follows ensures compliance with the Companys Quality and Information Security Management Systems, ICH GCP guidelines, applicable local and international legislation, including data protection legislation, as well as any amendments or updates the above-In case of deviation from the approved protocol, ICH GCP guidelines and/or applicable legislation during the study conduct, the CRA is responsible for reporting it to [. .. ]
Job am 20.11.2025 bei Jobleads gefunden
• Köln, Nordrhein- Westfalen
Beratungs-/ Consultingtätigkeiten Abgeschlossenes Studium
[. .. ] IT Sicherheitslösungen Erarbeitung von Vorgaben für den Bereich Secure Systems Engineering und/oder OS Hardening Erarbeitung von Konzepten zur Prävention vor und Abwehr von Bedrohungen und Angriffen Mitarbeit [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] in unserem Security Operation Center und der Nutzung von SIEM Software zur Überwachung der IT Landschaft unserer Kunden Erarbeitung und Entwickelung von Use Cases zur Erkennung von Bedrohungen, Schwachstellen und Hacker Angriffen Unterstützung unserer Kunden vor Ort bei Verdacht auf IT Sicherheitsvorfälle, wie z. B. Hackerangriffen oder Kompromittierung ihres IT Netzwerks durch Schadsoftware [. .. ] (OSCP) , Certified Ethical Hacker (CEH) , EC Council Certified Security Analyst (ECSA) , Certified Cyber Forensics Professional (CCFP) , Certified Forensic Computer Examiner (CFCE) und/oder Computer Hacking Forensic Investigator (CHFI) Ausdrucksstarke Berufs und Projekterfahrung in diesem Umfeld Sehr gute Applikations und Betriebssystemkenntnisse im Windows, Linux und Netzwerkumfeld Sehr gute Kenntnisse von Netzwerkprotokollen und Diensten Zusätzliche Kenntnisse Kenntnisse im Bereich Cloud Security Kenntnisse im Bereich Mobile Security Kenntnisse zu standardisierten Empfehlungen wie IT Grundschutz, ISO 2700x, ISO 25999 Kenntnisse rechtlicher [. .. ]
Job am 09.11.2025 bei Jobleads gefunden
Senior Short-Term Expert Theoretical Training on Mercure Software
Beratungs-/ Consultingtätigkeiten
[. .. ] and recommendations; Ensure all sessions are tailored to be provided in English with simultaneous interpretation provided. Expert Profile Required Qualifications and Experience Minimum 10 years of professional [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] experience as an investigator within an EU police service; Proven expertise in criminal intelligence analysis and in formulating law enforcement security measures; At least 8 years of operational experience using Mercure software, with in-depth knowledge of its procedures and applications; At least 5 years of experience in training delivery and capacity building in an international context; Excellent communication skills and fluency in spoken and written English. #J-18808-Ljbffr [. .. ]
Job am 08.11.2025 bei Jobleads gefunden
Beratungs-/ Consultingtätigkeiten
[. .. ] will be responsible for the following tasks: Conduct an updated evaluation of police (central and local level) and judicial capabilities in dealing with cybercrime; Evaluate, analyse and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] assess the cyber security measures implemented within the ASPs IT infrastructure; Conduct meetings to meet the specific needs (training and equipment) of ASP police officers; Design an activity plan to support the reinforcement of capacities in cybercrime. The supporting activities can include training (basic-advanced) , workshop, study visit in an EU MS, equipment, [. .. ] Mid-term expert will be responsible for coordinating and supervising the work of this expert. Expert Profile Required Qualifications and Experience At least 10 years of professional experience as an investigator within an EU law enforcement agency; Demonstrated experience in needs assessment, programme management, and the development of action plans within the framework of international cooperation projects supporting police services; Proven expertise, at least 10 years, in the field of cybercrime and e-evidence collection; Excellent communication skills and fluency in [. .. ]
Job am 09.10.2025 bei Jobleads gefunden
Sachverständiger Explosionsschutz/ MSR/ Cybersecurity (w/m/d)
• Trier, Rheinland- Pfalz
[. .. ] support for major infrastructure projects. This applies to the functional safety of industrial plants in an era of rapidly increasing interconnectivity of components and machines the keyword [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] being Operational Technology Security as well as to energy generation, utilization, and distribution, infrastructure, and network expansion. Our Core Areas Pressure Equipment Plant Engineering: Inspection, testing, and certification services focusing on pressure equipment such as pressure vessels, boilers, tanks, and piping systems. Elevators Conveyor Technology: Inspection, testing, and certification services for elevators, conveyor belts, [. .. ] Luxembourg, Luxembourg, Luxembourg 2 weeks ago Contern, Luxembourg, Luxembourg 2 weeks ago Senior Associate-Cybersecurity Operations (m/f/d) Luxembourg, Luxembourg, Luxembourg 2 weeks ago CSIRT Incident Handler Digital Forensic Investigator m/W Hesperange, Luxembourg, Luxembourg 1 month ago Cyber Security Consultant/ Senior Consultant IT Infrastructure Cloud and Cybersecurity Engineer Betzdorf, Grevenmacher, Luxembourg 3 weeks ago Luxembourg, Luxembourg, Luxembourg 2 weeks ago Manager-Cyber Information security Architecture Analyst in Cyber Governance Compliance Luxembourg, Luxembourg, Luxembourg 3 weeks ago Were unlocking community [. .. ]
Job am 07.12.2025 bei Neuvoo.com gefunden
Veeda Lifesciences
Clinical Research Associate
• Dortmund
[. .. ] the applicable Standard Operating Procedures (SOPs) and the applicable laws and regulations. He/ she is the primary responsible person for communication on operational study related activities between [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] the Sponsor, the Investigator and other study personnel to build and maintain successful working relationships. The most important responsibility is to ensure that the subjects rights are respected and that all collected clinical trial data are accurate, complete, and verifiable from source documents. Main responsibilities:-Acknowledges, follows ensures compliance with the Companys Quality and Information Security Management Systems, ICH GCP guidelines, applicable local and international legislation, including data protection legislation, as well as any amendments or updates the above-In case of deviation from the approved protocol, ICH GCP guidelines and/or applicable legislation during the study conduct, the CRA is responsible for reporting it to [. .. ]
Job am 07.12.2025 bei Neuvoo.com gefunden
Veeda Lifesciences
Clinical Research Associate
• Hamburg
[. .. ] the applicable Standard Operating Procedures (SOPs) and the applicable laws and regulations. He/ she is the primary responsible person for communication on operational study related activities between [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] the Sponsor, the Investigator and other study personnel to build and maintain successful working relationships. The most important responsibility is to ensure that the subjects rights are respected and that all collected clinical trial data are accurate, complete, and verifiable from source documents. Main responsibilities:-Acknowledges, follows ensures compliance with the Companys Quality and Information Security Management Systems, ICH GCP guidelines, applicable local and international legislation, including data protection legislation, as well as any amendments or updates the above-In case of deviation from the approved protocol, ICH GCP guidelines and/or applicable legislation during the study conduct, the CRA is responsible for reporting it to [. .. ]
Job am 07.12.2025 bei Neuvoo.com gefunden
Veeda Lifesciences
Clinical Research Associate
• Düsseldorf
[. .. ] the applicable Standard Operating Procedures (SOPs) and the applicable laws and regulations. He/ she is the primary responsible person for communication on operational study related activities between [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] the Sponsor, the Investigator and other study personnel to build and maintain successful working relationships. The most important responsibility is to ensure that the subjects rights are respected and that all collected clinical trial data are accurate, complete, and verifiable from source documents. Main responsibilities:-Acknowledges, follows ensures compliance with the Companys Quality and Information Security Management Systems, ICH GCP guidelines, applicable local and international legislation, including data protection legislation, as well as any amendments or updates the above-In case of deviation from the approved protocol, ICH GCP guidelines and/or applicable legislation during the study conduct, the CRA is responsible for reporting it to [. .. ]
Job am 07.12.2025 bei Neuvoo.com gefunden
Veeda Lifesciences
Clinical Research Associate
• Essen
[. .. ] the applicable Standard Operating Procedures (SOPs) and the applicable laws and regulations. He/ she is the primary responsible person for communication on operational study related activities between [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] the Sponsor, the Investigator and other study personnel to build and maintain successful working relationships. The most important responsibility is to ensure that the subjects rights are respected and that all collected clinical trial data are accurate, complete, and verifiable from source documents. Main responsibilities:-Acknowledges, follows ensures compliance with the Companys Quality and Information Security Management Systems, ICH GCP guidelines, applicable local and international legislation, including data protection legislation, as well as any amendments or updates the above-In case of deviation from the approved protocol, ICH GCP guidelines and/or applicable legislation during the study conduct, the CRA is responsible for reporting it to [. .. ]
Job am 07.12.2025 bei Neuvoo.com gefunden
Veeda Lifesciences
Clinical Research Associate
• Stuttgart
[. .. ] the applicable Standard Operating Procedures (SOPs) and the applicable laws and regulations. He/ she is the primary responsible person for communication on operational study related activities between [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] the Sponsor, the Investigator and other study personnel to build and maintain successful working relationships. The most important responsibility is to ensure that the subjects rights are respected and that all collected clinical trial data are accurate, complete, and verifiable from source documents. Main responsibilities:-Acknowledges, follows ensures compliance with the Companys Quality and Information Security Management Systems, ICH GCP guidelines, applicable local and international legislation, including data protection legislation, as well as any amendments or updates the above-In case of deviation from the approved protocol, ICH GCP guidelines and/or applicable legislation during the study conduct, the CRA is responsible for reporting it to [. .. ]
Job am 07.12.2025 bei Neuvoo.com gefunden
Veeda Lifesciences
Clinical Research Associate
• Leipzig
[. .. ] the applicable Standard Operating Procedures (SOPs) and the applicable laws and regulations. He/ she is the primary responsible person for communication on operational study related activities between [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] the Sponsor, the Investigator and other study personnel to build and maintain successful working relationships. The most important responsibility is to ensure that the subjects rights are respected and that all collected clinical trial data are accurate, complete, and verifiable from source documents. Main responsibilities:-Acknowledges, follows ensures compliance with the Companys Quality and Information Security Management Systems, ICH GCP guidelines, applicable local and international legislation, including data protection legislation, as well as any amendments or updates the above-In case of deviation from the approved protocol, ICH GCP guidelines and/or applicable legislation during the study conduct, the CRA is responsible for reporting it to [. .. ]
Job am 07.12.2025 bei Neuvoo.com gefunden
Veeda Lifesciences
Clinical Research Associate
• Cologne
[. .. ] the applicable Standard Operating Procedures (SOPs) and the applicable laws and regulations. He/ she is the primary responsible person for communication on operational study related activities between [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] the Sponsor, the Investigator and other study personnel to build and maintain successful working relationships. The most important responsibility is to ensure that the subjects rights are respected and that all collected clinical trial data are accurate, complete, and verifiable from source documents. Main responsibilities:-Acknowledges, follows ensures compliance with the Companys Quality and Information Security Management Systems, ICH GCP guidelines, applicable local and international legislation, including data protection legislation, as well as any amendments or updates the above-In case of deviation from the approved protocol, ICH GCP guidelines and/or applicable legislation during the study conduct, the CRA is responsible for reporting it to [. .. ]
Job am 07.12.2025 bei Neuvoo.com gefunden
Veeda Lifesciences
Clinical Research Associate
• Frankfurt
[. .. ] the applicable Standard Operating Procedures (SOPs) and the applicable laws and regulations. He/ she is the primary responsible person for communication on operational study related activities between [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] the Sponsor, the Investigator and other study personnel to build and maintain successful working relationships. The most important responsibility is to ensure that the subjects rights are respected and that all collected clinical trial data are accurate, complete, and verifiable from source documents. Main responsibilities:-Acknowledges, follows ensures compliance with the Companys Quality and Information Security Management Systems, ICH GCP guidelines, applicable local and international legislation, including data protection legislation, as well as any amendments or updates the above-In case of deviation from the approved protocol, ICH GCP guidelines and/or applicable legislation during the study conduct, the CRA is responsible for reporting it to [. .. ]
Job am 07.12.2025 bei Neuvoo.com gefunden
Veeda Lifesciences
Clinical Research Associate
• Berlin
[. .. ] the applicable Standard Operating Procedures (SOPs) and the applicable laws and regulations. He/ she is the primary responsible person for communication on operational study related activities between [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] the Sponsor, the Investigator and other study personnel to build and maintain successful working relationships. The most important responsibility is to ensure that the subjects rights are respected and that all collected clinical trial data are accurate, complete, and verifiable from source documents. Main responsibilities:-Acknowledges, follows ensures compliance with the Companys Quality and Information Security Management Systems, ICH GCP guidelines, applicable local and international legislation, including data protection legislation, as well as any amendments or updates the above-In case of deviation from the approved protocol, ICH GCP guidelines and/or applicable legislation during the study conduct, the CRA is responsible for reporting it to [. .. ]
Job am 07.12.2025 bei Neuvoo.com gefunden
Veeda Lifesciences
Clinical Research Associate
• Munich
[. .. ] the applicable Standard Operating Procedures (SOPs) and the applicable laws and regulations. He/ she is the primary responsible person for communication on operational study related activities between [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] the Sponsor, the Investigator and other study personnel to build and maintain successful working relationships. The most important responsibility is to ensure that the subjects rights are respected and that all collected clinical trial data are accurate, complete, and verifiable from source documents. Main responsibilities:-Acknowledges, follows ensures compliance with the Companys Quality and Information Security Management Systems, ICH GCP guidelines, applicable local and international legislation, including data protection legislation, as well as any amendments or updates the above-In case of deviation from the approved protocol, ICH GCP guidelines and/or applicable legislation during the study conduct, the CRA is responsible for reporting it to [. .. ]
Job am 07.12.2025 bei Neuvoo.com gefunden
Veeda Lifesciences
Clinical Research Associate
[. .. ] the applicable Standard Operating Procedures (SOPs) and the applicable laws and regulations. He/ she is the primary responsible person for communication on operational study related activities between [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] the Sponsor, the Investigator and other study personnel to build and maintain successful working relationships. The most important responsibility is to ensure that the subjects rights are respected and that all collected clinical trial data are accurate, complete, and verifiable from source documents. Main responsibilities:-Acknowledges, follows ensures compliance with the Companys Quality and Information Security Management Systems, ICH GCP guidelines, applicable local and international legislation, including data protection legislation, as well as any amendments or updates the above-In case of deviation from the approved protocol, ICH GCP guidelines and/or applicable legislation during the study conduct, the CRA is responsible for reporting it to [. .. ]
Häufig gestellte Fragen
Wieviel verdient man als Security Investigator pro Jahr?
Als Security Investigator verdient man zwischen EUR 50.000,- bis EUR 80.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Security Investigator Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 23 offene Stellenanzeigen für Security Investigator Jobs.
In welchen Bundesländern werden die meisten Security Investigator Jobs angeboten?
Die meisten Stellenanzeigen für Security Investigator Jobs werden derzeit in Nordrhein-Westfalen (6 Jobs), Niedersachsen (3 Jobs) und Bayern (2 Jobs) angeboten.
Zu welchem Berufsfeld gehören Security Investigator Jobs?
Security Investigator Jobs gehören zum Berufsfeld Polizei, Militär, Sicherheit.
