24 Jobs für Security Investigator
Stellenangebote Security Investigator Jobs
Neu Job vor 4 Std. bei Jobleads gefunden
• 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 gestern bei Jobleads gefunden
Clinical Research Associate
• Dortmund, 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 gestern bei Jobleads gefunden
Clinical Research Associate
• Leipzig, Sachsen
[. .. ] 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 2 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 5 Tagen bei Jobleads gefunden
Clinical Research Associate
• Düsseldorf, Nordrhein- Westfalen Duesseldorf
[. .. ] 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 5 Tagen bei Jobleads gefunden
Clinical Research Associate
• 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 7 Tagen bei Jobleads gefunden
• Boudry, Neuenburg
Führungs-/ Leitungspositionen
[. .. ] Evidence Generation (MEG) Lead in Oncology at Bristol Myers Squibb oversees evidence generation for the Oncology portfolio, including Clinical Research Collaborations (CRCs) , Medical Affairs Sponsored Studies [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] (MAST) , and Investigator-Sponsored Research Studies (ISRs) , ensuring alignment with internal strategies to accelerate pipeline development. Key responsibilities include fostering relationships with thought leaders, managing the lifecycle of CRCs and ISRs, and addressing evidence gaps by partnering with academic and professional networks. Responsibilities Responsibilities will include, but are not limited to, the [. .. ] for this position, please visit this page for important additional information https/ / careers. bms. com/california-residents/ . Data Protection We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at https/ / careers. bms. com/fraud-protection. Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations. #J-18808-Ljbffr 71986461 [. .. ]
Job vor 10 Tagen bei Jobleads gefunden
Multi-physic Modelling Research Scientist
• 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 vor 11 Tagen bei Jobleads gefunden
• Boudry, Neuenburg
Führungs-/ Leitungspositionen
[. .. ] Director, Cell Therapy, Medical Evidence Generation (MEG Global Medical Affairs) will lead the development and implementation of evidence generation book of work (including Medical Affairs Sponsored studies, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] clinical research collaborations, investigator-sponsored studies and select health outcomes studies) associated with the Cell Therapy portfolio/ pipeline and provides leadership for the respective MEG Team. In this role, he/ she will oversee the development of the Integrated Evidence Plans (IEPs) and will be responsible for the prioritization, development, review, and execution of all [. .. ] hired for this position, please visit this page for important additional information: https:/ / careers. bms. com/california-residents/ Data Protection We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at https:/ / careers. bms. com/fraud-protection. Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations. #J-18808-Ljbffr 71598479 [. .. ]
Job am 22.11.2025 bei Jobleads gefunden
AS400 Infrastructure operations Support Engineer
• Hamburg
[. .. ] an experienced AS Infrastructure Operations Support Engineer to manage and support our AS systems. The ideal candidate will have extensive experience in AS infrastructure management, performance optimization, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] backup and recovery, security and troubleshooting using specific tools and technologies. Key Responsibilities Infrastructure Management Installation, configuration and upgrades: Set up and maintain AS systems, including software upgrades and patches, using tools like IBM i Access Client Solutions Client and IBM Navigator for i. Storage Management Allocate storage space, manage libraries and objects, and [. .. ] 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 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 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 08.11.2025 bei Jobleads gefunden
Senior mid-term to conduct an Assessment mission on cybercrime and cybersecurity capabilities a. . .
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
• 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 vor 8 Tagen 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 vor 8 Tagen 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 vor 8 Tagen 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 vor 8 Tagen 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 vor 8 Tagen 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 vor 8 Tagen 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 vor 8 Tagen 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 vor 8 Tagen 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 [. .. ]
Job vor 8 Tagen 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 vor 8 Tagen 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 vor 8 Tagen 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 [. .. ]
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 24 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), Hamburg (4 Jobs) und Niedersachsen (3 Jobs) angeboten.
Zu welchem Berufsfeld gehören Security Investigator Jobs?
Security Investigator Jobs gehören zum Berufsfeld Polizei, Militär, Sicherheit.
