Security Investigator Stellenangebote


+ Suchfilter (0 aktiv)

13 Jobs für Security Investigator


Stellenangebote Security Investigator Jobs


Job gestern bei Mindmatch.ai gefunden Bristol Myers Squibb EU Policy

Senior Director, EEA Deputy QPPV (m/f/d)

• AT- 9 Wien Führungs-/ Leitungspositionen [. .. ] abstracts and manuscripts) to ensure alignment with study objectives and regulatory expectations. The Deputy QPPV also reviews and provides scientific input to justification documents, variation and renewal [...]
MEHR INFOS ZUM STELLENANGEBOT[...] submissions, Sm PCs, DHPCs, Investigator Letters, response documents, core additional educational materials, health hazard evaluations, and other relevant safetyrelated documents. Ensures complete, accurate, and timely responses to requests from competent authorities in Member States and from the EMA for information necessary to support the benefitrisk evaluation of medicinal products. Contributes to the oversight and control [. .. ] 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. If this posting is missing required information required by local [. .. ]

▶ Zur Stellenanzeige
Neu Job vor 2 Std. bei Jobleads gefunden

Senior CRA-Germany

[. .. ] each subject/ patient as required/appropriate. Demonstrates diligence in protecting the confidentiality of each subject/ patient. Assess 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 [. .. ]

▶ Zur Stellenanzeige
Job gestern bei Jobleads gefunden

Senior Manager, Medical Science Liaison East, Germany

• München, Bayern [. .. ] approved field medical plans within an assigned territory in Germany, engage in peer-to-peer scientific exchange with healthcare professionals, that translate into medical insights, support clinical study site [...]
MEHR INFOS ZUM STELLENANGEBOT[...] and investigator engagement, and contribute to medical education, advisory boards, and medical congress activities under the direction of the Senior Director, Medical Affairs, Germany. Medical Science Liaisons (MSLs) are an essential member of the Medical Affairs team who will work as an extension of the Medical Affairs organization. The MSL team will [. .. ] change, able to operate within agreed financial budgets. Ability to set priorities and work towards tight timelines with a willingness to travel, mainly within Germany. Revolution Medicines takes protection and security of personal data very seriously and respects your right to privacy while using our website and when contacting us by email or phone. We will only collect, process and use any personal data that you provide to us in accordance with our CCA Notice and Privacy Policy. For additional information, [. .. ]

▶ Zur Stellenanzeige
Job gestern bei Jobleads gefunden

Medical Science Liaison, Switzerland

• Basel, Basel- Stadt [. .. ] execute approved field medical plans within an assigned Swiss territory, engage in peer-to-peer scientific exchange with healthcare professionals, gather and communicate medical insights, support clinical study site [...]
MEHR INFOS ZUM STELLENANGEBOT[...] and investigator engagement, and contribute to medical education, advisory boards, and congress activities under the direction of the Medical Director, Switzerland. Medical Science Liaisons (MSLs) are an essential member of the Medical Affairs team who will work as an extension of the Medical Affairs organization. The MSL team will serve as a [. .. ] KOLs and healthcare professionals. Self-directed and able to thrive in a fast-paced and dynamic environment. Willingness to travel up to 60 of time. Revolution Medicines takes protection and security of personal data very seriously and respects your right to privacy while using our website and when contacting us by email or phone. We will only collect, process and use any personal data that you provide to us in accordance with our CCPA Notice and Privacy Policy. For additional information, [. .. ]

▶ Zur Stellenanzeige
Job gestern bei Jobleads gefunden Senior Director, EEA Deputy QPPV (m/f/d) • Wien Führungs-/ Leitungspositionen [. .. ] abstracts and manuscripts) to ensure alignment with study objectives and regulatory expectations. The Deputy QPPV also reviews and provides scientific input to justification documents, variation and renewal [...]
MEHR INFOS ZUM STELLENANGEBOT[...] submissions, Sm PCs, DHPCs, Investigator Letters, response documents, core additional educational materials, health hazard evaluations, and other relevant safetyrelated documents. Ensures complete, accurate, and timely responses to requests from competent authorities in Member States and from the EMA for information necessary to support the benefitrisk evaluation of medicinal products. Contributes to the oversight and control [. .. ] 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. If this posting is missing required information required by local [. .. ]

▶ Zur Stellenanzeige
Job vor 7 Tagen bei Jobleads gefunden

Clinical Research Associate-Berlin/ Leipzig/ Dresden

[. .. ] 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 [. .. ]

▶ Zur Stellenanzeige
Button Jobabo Nichts verpassen: Jobs per eMail
► Speichern Sie jetzt Ihre Jobsuche!

Job vor 7 Tagen bei Jobleads gefunden

Clinical Research Associate Multi-Sponsor

[. .. ] guide site staff toward closure Use hardware and software for clinical study data review and capture Verify compliance with electronic data capture requirements Perform investigational product inventory, [...]
MEHR INFOS ZUM STELLENANGEBOT[...] reconciliation and storage/ security reviews as needed Verify investigational product dispensing and administration according to protocol Review Investigator Site Files and reconcile them with the Trial Master File Document activities through letters, trip reports, communication logs and other project documents Support subject/ patient recruitment, retention and awareness strategies Track observations, ongoing status and action items to resolution Manage site-level activities and communications to meet project objectives, deliverables [. .. ]

▶ Zur Stellenanzeige
Job vor 8 Tagen bei Jobleads gefunden

Associate Director, Field Medical Advisor GI, Germany

Führungs-/ Leitungspositionen [. .. ] Plan and execute national medical meetings and symposia at national congresses. Plan and execute national advisory boards and medical congress participation to enhance scientific visibility. Lead approval [...]
MEHR INFOS ZUM STELLENANGEBOT[...] process of national investigator-initiated trials and clinical research activities in Germany in collaboration with global and regional teams. Align insights into the competitive and scientific landscape generated from the field to inform internal strategy and make them actionable. Partner with HEOR and RWE to develop real-world evidence and outcomes research projects. Partner [. .. ] or real-world evidence studies. Knowledge of German healthcare systems, reimbursement structures, and compliance requirements. Track record in publication planning, congress presentations, and scientific communications. Revolution Medicines takes protection and security of personal data very seriously and respects your right to privacy while using our website and when contacting us by email or phone. We will only collect, process and use any personal data that you provide to us in accordance with our CCPA Notice and Privacy Policy. For additional information, [. .. ]

▶ Zur Stellenanzeige
Job am 03.09.2026 bei Jobleads gefunden

Product Designer-Digital Health Platform (Part-Time)

• Berlin, Potsdam, Brandenburg [. .. ] richer EHR interoperability, and stronger regulatory rigor. Were looking for a Product Designer to help us shape that next chapter end-to-end-from the participant mobile experience through to [...]
MEHR INFOS ZUM STELLENANGEBOT[...] investigator and clinician workflows. Youll partner with our existing Product Designer on D4L Collect, and work shoulder-to-shoulder with product, engineering, QA, and regulatory to make D4L Collect the platform of choice for digital health and real-world studies. The position is full-time, based in Berlin/ Potsdam, with an [. .. ] available to research in a comprehensive, digital and secure way. Our interdisciplinary team in Potsdam, Berlin and Singapore brings together experts from fields such as product development, digital engineering, data security and science. Data4Life was founded in 2017 and is funded by the Hasso Plattner Foundation. We care about Diversity : Many different lives, careers, and development paths lead to Data4Life. We welcome experts from a wide range of backgrounds and experiences to our international team, offering everyone equal opportunities to [. .. ]

▶ Zur Stellenanzeige
Job am 18.08.2026 bei Jobleads gefunden

CRA II-multi-sponsor (north-east Germany)

• München, Bayern [. .. ] each subject/ patient, as required/appropriate. Demonstrate diligence in protecting the confidentiality of each subject/ patient. Assess 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. Assess site processes and conduct Source Document Review of appropriate site source documents and medical records. Verify required clinical data entered in the case report form (CRF) is accurate and complete. Apply query resolution techniques remotely and on site, and provide guidance to site staff as necessary, driving query resolution to closure within agreed timelines. May perform investigational product (IP) inventory, reconciliation and reviews of storage and security. Verify the IP has been dispensed and administered to subjects/ patients according to the protocol. Verify issues or risks associated with blinded or randomized information related to IP. Routinely review the Investigator Site File (ISF) for accuracy, timeliness and completeness. Reconcile contents of the ISF with the Trial Master File [. .. ]

▶ Zur Stellenanzeige
Job am 18.08.2026 bei Jobleads gefunden Clinical Research Associate (Germany) • Ahlen, Nordrhein- Westfalen Work-Life-Balance [. .. ] by RQM+ and sponsors. Works closely with the Project Manager and/or Lead CRA to ensure all monitoring activities are conducted according to study requirements. Primary Responsibilities: Participates [...]
MEHR INFOS ZUM STELLENANGEBOT[...] in the investigator recruitment process and performs site qualification visits of potential investigators. Evaluates the capability of the site to successfully manage and conduct clinical studies. Collaborates with the start-up department to coordinate activities with the site in preparation for the initiation of the study. Obtains regulatory documentation for successful implementation, monitoring, [. .. ] and quality professionals. At RQM+, you are not just another employee, you are a member of RQM+ family. Make your impact today Job Opportunity Verification At RQM+, we prioritize the security of our job applicants. To ensure a safe application process: All legitimate RQM+ job opportunities are listed on our official careers page: rqmplus. com/careers Every candidate going through the interview process will participate in a voice and/or video interview. Exercise caution with unsolicited job offers or requests for [. .. ]

▶ Zur Stellenanzeige
Job am 18.08.2026 bei Jobleads gefunden Legal Officer-Middle East Programme • Genf [. .. ] 4 years demonstrated experience in litigating human rights, humanitarian law, or international criminal law. Minimum of 4 years demonstrated experience investigating human rights violations or international crimes. [...]
MEHR INFOS ZUM STELLENANGEBOT[...] Experience as an investigator within an international tribunal or mechanism is desirable. Strong understanding of gender perspectives in armed conflict and fragile security contexts. Demonstrated experience working with partners on litigation initiatives. Experience in case preparation and development, including investigation, case strategy, legal drafting to an excellent standard. Proficient in MS Office packages (Excel, Word and Power Point) . Fluency in English and Arabic is highly desirable. Good knowledge and understanding of the [. .. ]

▶ Zur Stellenanzeige
Job am 18.08.2026 bei Jobleads gefunden Director, Medical Affairs, Be Lux • Schwyz Führungs-/ Leitungspositionen [. .. ] with country regulations and clinical practice Build and maintain strong relationships with national and regional key opinion leaders, oncology networks, academic institutions, and scientific societies Lead scientific [...]
MEHR INFOS ZUM STELLENANGEBOT[...] exchange, advisory boards, investigator and other external meetings, press conferences, and congress engagement at country level Collaborate effectively with Midsized Markets, Regional and Global teams by contributing to overall medical affairs strategy, strongly partnering with local, regional and global clinical development and operations teams Drive local medical strategy across pre-launch, launch, and post-[. .. ] unlawful discrimination based on race, color, religion, gender, sexual orientation, gender identity/ expression, national origin/ ancestry, age, disability, marital status, medical condition, and veteran status. Revolution Medicines takes protection and security of personal data very seriously and respects your right to privacy while using our website and when contacting us by email or phone. We will only collect, process and use any personal data that you provide to us in accordance with our CCPA Notice and Privacy Policy. For additional information, [. .. ]

▶ Zur Stellenanzeige
Jobs



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 13 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 Bayern (2 Jobs), Berlin (2 Jobs) und Sachsen (1 Jobs) angeboten.


Zu welchem Berufsfeld gehören Security Investigator Jobs?

Security Investigator Jobs gehören zum Berufsfeld Polizei, Militär, Sicherheit.


Jobs per Email


Verpassen Sie keine Jobs!
Wir informieren Sie kostenfrei über neue Jobangebote!


Datenschutzklärung lesen


Dauer: 0.0453 s., Vers. V.2025-d-2009-Ind-141