169 Jobs für Compliance Investigator
Stellenangebote Compliance Investigator Jobs
Job am 15.11.2025 bei Stellenanzeigen.de gefunden
Schwarz Corporate Solutions
• Baden- Württemberg 74172 Neckarsulm
Homeoffice möglich
Senior
Investigator Forensic Services Standort: Neckarsulm Abteilung/ Bereich: Level: Berufserfahrene Referenznummer: 1611 Mit einem Team, das täglich den Unterschied macht, stärken wir den Mitarbeitenden der Unternehmen der Schwarz Gruppe den [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Rücken. Unser Arbeitsalltag ist geprägt von abwechslungsreichen Aufgaben sowie vielfältigen Bereichen und unendlichen Möglichkeiten. Was unsere 4.000 Mitarbeitenden miteinander teilen, sind [. .. ] bist du dabei? Where Excellence Works. Der Bereich Interne Untersuchungen führt innerhalb der Schwarz Corporate Solutions forensische Untersuchungen bzw. präventive Assessments und Workshops in allen Fällen der Wirtschaftskriminalität und HR Compliance durch, unter Berücksichtigung von Optimierungs- und Präventionsmaßnahmen. Darüber hinaus unterstützt und berät der Bereich Interne Untersuchungen im Rahmen der operativen und strategischen Tätigkeit. Deine Aufgaben Eigenständige Durchführung forensischer Untersuchungen zur Aufklärung relevanter Delikte in Themenfeldern wie Wirtschaftskriminalität/ Fraud, Korruption, HR Compliance im nationalen und internationalen Unternehmensumfeld. Routinierte Beherrschung eines breiten [. .. ]
Neu Job vor 6 Std. bei Jooble gefunden
Alimentiv
Clinical Operations Lead
• Hamburg
Führungs-/ Leitungspositionen
Responsible for the clinical operations of a project within a defined regional/ global level. Provides oversight of project deliverables, assigned Clinical Research Associate (CRAs) and
Investigator sites in accordance with [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] the Monitoring Plan, Protocol, Good Clinical Practice (GCP) , ICH guidelines and local regulations. The COL acts as a primary liaison between the CRAs and the clinical project team. Additional responsibilities include project specific training of CRAs, conducting assessment visits with CRAs, implementation of enrollment and [. .. ] review and track protocol deviations, and support other objectives for clinical operations and the clinical project team. Project Oversight Overall oversight of (a group of) regional CRAs to ensure (site) compliance with study protocol, study plans, ICH-GCP, local regulations and study timelines. Monitoring support visits (Co-monitoring) , per project requirements, to aid the site/ CRA in the satisfactory performance and compliance with standards mentioned above. May support clinical project team by providing oversight of study deliverables related to other [. .. ]
Neu Job vor 6 Std. bei Jooble gefunden
SAP
• Mörfelden- Walldorf
[. .. ] truly belong. What s in it for you? Constant learning, skill growth, great benefits, and a team that wants you to grow and succeed. Job Description The [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Security Incident Response Investigator role will be dedicated to the real time analysis, lead investigation and escalation coordination of detected cyber threat events and intelligence, supporting operational efforts around the Security Detection and remediation to various system owners and other stakeholders and ensuring real time capability enhancement to respond to evolving threats. The Security [. .. ] Knowledge in and current knowledge of security threat intelligence and recent attack vectors including network, application and social methods. Knowledge in and an understanding or proficiency in information security and compliance regulations, frameworks and leading practices Bring out your best SAP innovations help more than four hundred thousand customers worldwide work together more efficiently and use business insight more effectively. Originally known for leadership in enterprise resource planning (ERP) software, SAP has evolved to become a market leader in end-to-[. .. ]
Job gestern bei Jooble gefunden
Study Physician sponsor dedicated in Germany
• München
[. .. ] requirements too) Medical Monitoring experience preferred Pharma company experience preferred. However, CRO experience is fine. If no industry experience, the in addition to clinical practice they should [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] have worked principal investigator/ sub investigator in clinical trials for a reasonable amount of time. Travel-15-20 depending on the study requirements. Key words to look for in potential CVs-Clinical Trial protocol-writing/ reviewing, Identify medically relevant critical data, Medical risks, risk mitigation/ monitoring plan, Medical quality review/clinical quality monitoring, Jreview, [. .. ] of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job. Summary Study Physician Medical Doctors (Candidates who completed fellowship, residency, specialization e. g. Internal medicine, oncology, neurology, immune-oncology, cardiology, pediatrics, emergency medicine [. .. ]
Job vor 3 Tagen bei Jooble gefunden
• Berlin
[. .. ] aligned to strategy within the business Serves as external, credible scientific expert on disease area and client products at HCP field meetings, key medical and scientific conferences, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] advisory boards, clinical investigator meetings and patient advocacy group meetings Facilitate clear communication between the client and investigators in investigator engagement for both client trials and investigator-sponsored studies and barriers to enrolment for pipeline assets Works to the highest ethical compliance, ethics and safety standards adhering to all local regulations and laws Maintains and develops synergistic relationships with KOLs to expand research, advisory, and educational partnership opportunities Training of the Key Account Management Team on scientific and medical topics Requirements: Advanced Degree MD, Ph D, Pharm D Demonstrable experience in an MSL function [. .. ]
Job vor 4 Tagen bei Jooble gefunden
Sr CRA in oncology-Sponsor dedicated-Home Based Germany
• München
[. .. ] 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 Practices (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 via [. .. ]
▶ Zur Stellenanzeige
Job vor 14 Tagen bei Jooble gefunden
Thermo Fisher Scientific
• Karlsruhe
[. .. ] We invite you to re-imagine health promoting protocols with us, working alongside our dedicated, forward-thinking and upbeat teams. A day in the Life: Performs PPD clinical research [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] services investigator file reviews and logging of outstanding issues in project related tracking tools Reviews regulatory documents for proper content Liaises with monitor and investigative sites to resolve outstanding regulatory issues identified Disseminates study related information, including project tracking updates to Clients, clinical study teams and other PPD clinical research services departments Assists with the identification of potential investigators and development/ distribution of initial protocol packets May assist the project team with the preparation of regulatory compliance review packages Builds meeting agendas and minutes, as well as coordinates team conference calls and distribution of meeting minutes Keys to Success: Education University degree in life sciences, or equivalent in education, training and experience Knowledge, Skills, Abilities Responsible for adhering to Good Clinical Practices, country specific regulations, PPD clinical [. .. ]
Job am 17.01.2026 bei Jooble gefunden
Alira Health
Project Manager Senior
• München
[. .. ] Associates. Creates and reviews clinical study documents, including protocols, ICF templates, study budgets, site log/ form templates, study manuals and plans, site binders, etc. Presents at project [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] meetings such as investigator meetings and new client meetings. Updates management accurately and regularly through frequent communication. Manages subject accrual, retention, and compliance. Assists in TMF management and manages TMF reviews as needed. Complies with and ensures team compliance with ICH GCP guidelines, FDA regulations, and company SOPs. 3 years of experience in the pharmaceutical/ biotechnology/ CRO industry with 1 year of management experience Strong analytical, negotiation, meeting management, cross-functional team, and [. .. ]
Job am 17.01.2026 bei Jooble gefunden
Alira Health
• München
[. .. ] Associates. Creates and reviews clinical study documents, including protocols, ICF templates, study budgets, site log/ form templates, study manuals and plans, site binders, etc. Presents at project [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] meetings such as investigator meetings and new client meetings. Updates management accurately and regularly through frequent communication. Manages subject accrual, retention, and compliance. Assists in TMF management and manages TMF reviews as needed. Complies with and ensures team compliance with ICH GCP guidelines, FDA regulations, and company SOPs. 3 years of experience in the pharmaceutical/ biotechnology/ CRO industry with 1 year of management experience Strong analytical, negotiation, meeting management, cross-functional team, and [. .. ]
Job am 17.01.2026 bei Jooble gefunden
Alira Health
Senior Project Management Officer
• München
[. .. ] Associates. Creates and reviews clinical study documents, including protocols, ICF templates, study budgets, site log/ form templates, study manuals and plans, site binders, etc. Presents at project [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] meetings such as investigator meetings and new client meetings. Updates management accurately and regularly through frequent communication. Manages subject accrual, retention, and compliance. Assists in TMF management and manages TMF reviews as needed. Complies with and ensures team compliance with ICH GCP guidelines, FDA regulations, and company SOPs. 3 years of experience in the pharmaceutical/ biotechnology/ CRO industry with 1 year of management experience Strong analytical, negotiation, meeting management, cross-functional team, and [. .. ]
Job am 17.01.2026 bei Jooble gefunden
Alira Health
• München
[. .. ] and communications to ensure timely attainment of trial milestones. Ensures accuracy of reports and material work product. Provides monthly billing information to finance team. Presents at project [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] meetings such as investigator meetings and new client meetings. Updates management accurately and regularly through frequent communication. Identifies issues and develops problem-solving strategies to ensure study timelines are met. Manages subject accrual, retention, and compliance. Assists in TMF management and manages TMF reviews as needed. Prepares for and participates in third-party audits and FDA inspections. Complies with and ensures team compliance with ICH GCP guidelines, FDA regulations, and company SOPs. Participates in internal, client/ sponsor, scientific, and other meetings as required. Performs additional duties [. .. ]
Job am 17.01.2026 bei Jooble gefunden
Alira Health
Senior Project Director
• München
Führungs-/ Leitungspositionen
[. .. ] Associates. Creates and reviews clinical study documents, including protocols, ICF templates, study budgets, site log/ form templates, study manuals and plans, site binders, etc. Presents at project [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] meetings such as investigator meetings and new client meetings. Updates management accurately and regularly through frequent communication. Manages subject accrual, retention, and compliance. Assists in TMF management and manages TMF reviews as needed. Complies with and ensures team compliance with ICH GCP guidelines, FDA regulations, and company SOPs. 3 years of experience in the pharmaceutical/ biotechnology/ CRO industry with 1 year of management experience Strong analytical, negotiation, meeting management, cross-functional team, and [. .. ]
Job am 17.01.2026 bei Jooble gefunden
Alira Health
• München
[. .. ] Associates. Creates and reviews clinical study documents, including protocols, ICF templates, study budgets, site log/ form templates, study manuals and plans, site binders, etc. Presents at project [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] meetings such as investigator meetings and new client meetings. Updates management accurately and regularly through frequent communication. Manages subject accrual, retention, and compliance. Assists in TMF management and manages TMF reviews as needed. Complies with and ensures team compliance with ICH GCP guidelines, FDA regulations, and company SOPs. 3 years of experience in the pharmaceutical/ biotechnology/ CRO industry with 1 year of management experience Strong analytical, negotiation, meeting management, cross-functional team, and [. .. ]
Job am 16.01.2026 bei Jooble gefunden
Euro London
Spanish speaking Financial Crime Investigator
• Vereinigte Königreich
About the Role: Spanish speaking Financial Crime
Investigator Brand new positions for 2026 Fully remote If youre an experienced Financial Crime Investigator fluent in Spanish and English, and youre [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] excited by the chance to join a highgrowth organisation right at the start of something BIG, this is an exceptional opportunity to accelerate your career. Euro London is partnering [. .. ] business and customer accounts, identifying and escalating suspicious activity. Review and recommend Suspicious Transaction Reports (STRs) for submission to relevant regulatory authorities. Assess and approve onboarding of new customers, ensuring compliance with AML and regulatory standards. Perform ongoing due diligence on high-risk accounts to proactively identify and mitigate potential financial crime risks. Provide financial crime expertise and guidance to operational teams, supporting consistent and effective compliance practices across the organisation. Essential Skills Experience: Fluent in Spanish and English (written and [. .. ]
Job am 14.01.2026 bei Jooble gefunden
• München
Freiberuflich
[. .. ] site qualification, site initiation, interim monitoring, site management activities 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. [. .. ]
▶ Zur Stellenanzeige
Job am 14.01.2026 bei Jooble gefunden
The Lemon Consulting
German Speaker Customer Support Agents-(Included relocation package )
• Homeoffice
[. .. ] 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 Requirements Your qualifications: You speak German fluently and you are fluent in English (B2) . Experience in customer support is a [. .. ] 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 Benefits We Offer: Fully paid relocation package Get 2 extra salaries per year (total of 14 salaries) Performance bonuses Development opportunities within the company (supervisor, quality analyst, CSR2, trainer) [. .. ]
Job am 14.01.2026 bei Jooble gefunden
Städtisches Klinikum Görlitz gGmbH
• Görlitz
Abgeschlossene Ausbildung
Jobticket Vermögenswirksame Leistungen Work-Life-Balance
[. .. ] Koordination und enge Zusammenarbeit mit Prüfärzten, Sponsoren, CROs und Studienzentralen zur Sicherstellung eines reibungslosen Studienablaufs. Vorbereitung, Assistenz und Nachbereitung von Monitorbesuchen, Audits und behördlichen Inspektionen einschließlich Pflege [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] der relevanten Studiendokumente (Investigator Site File) . Durchführung studienspezifischer Untersuchungen wie EKG, Messung von Vitalparametern sowie sachgerechte Blutentnahmen und Probenverarbeitung nach Studienvorgaben. Screening und Betreuung von Studienteilnehmenden, inklusive Aufklärungsvorbereitung, Terminplanung und kontinuierlicher Kommunikation. Erfassung, Pflege und Qualitätssicherung der Studiendaten in elektronischen oder papierbasierten CRFs. Bestellwesen und Verwaltung studienspezifischer Materialien, Medikamente (IMP) und Laborkits. Sicherstellung der Einhaltung aller Qualitäts-, Sicherheits- und Compliance-Standards während der gesamten Studiendurchführung. Ihr Profil Sie verfügen über eine erfolgreich abgeschlossene Ausbildung als Medizinische/ r Fachangestellte/ r (MFA) , Gesundheits- und Krankenpfleger/in, Pflegefachkraft oder eine vergleichbare medizinische Qualifikation. Sie bringen Berufserfahrung in der klinischen Forschung bzw. als Study Nurse/ Studienkoordinator/in mit. Eine hohe Patientenorientierung, ausgeprägtes Einfühlungsvermögen [. .. ]
Job am 14.01.2026 bei Jooble gefunden
Incyte Corporation
(Senior) Medical Manager Dermatology (m/f/d)
• München
[. .. ] activities (e. g. educational programs, communication campaigns, scientific symposia etc. ) Ensures that Health Care Professionals (HCP) and educational activities are of high scientific quality and are [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] in line with compliance regulations Demonstrates ability to strategically engage with and manage networks of Key External Experts (KEEs) , professional association, patient organization, and other vital healthcare stakeholders in the region Designs and implement clinical research projects within defined standards and budgets (e. g. Phase IV, post marketing clinical activities such as registry/ database projects, epidemiological surveys, and PMOS studies) . Provide the required oversight to manage review, approval and conduct of IIR studies Collaborate with clinical trial teams and support investigator engagements (e. g. review new clinical study protocols, identifying potential investigators/ sites, conducting feasibility surveys) Supports adaptation of international/ local training and scientific material in collaboration with marketing and other internal stakeholders Supports development of publication plans and covers country data generation needs Provides scientific in-house training for MSLs, [. .. ]
Job am 14.01.2026 bei Jooble gefunden
Incyte Corporation
• München
Führungs-/ Leitungspositionen
[. .. ] non-promotional plans for assigned products and therapeutic areas Ensures appropriate execution of medical content elements of the tactical plan for assigned product (s) and therapeutic area (s) [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Acts within compliance, regulatory and legal requirements as well as within company guidelines Demonstrates medical and scientific expertise to core business strategy and marketing/ business development plans, strongly contributes to the development of and updates to the strategic medical plans Ensuring that strategically aligned scientific communication points, elements from other internal guidance and [. .. ] leadership and actively contributes to market access dossiers Oversee the agenda development, content creation, and execution for educational symposia, internal meetings/ summits and advisory boards Supports advisory board meetings and investigator meetings. Provides support for content development and delivering clinical presentations at medical meetings Develops and delivers presentations to colleagues and management as needed, provides strong input to briefing documents, written communications, Frequently Asked Questions documents, backgrounders, newsletters, slide decks, and medical information letters etc. MD, Pharm D or Ph D in life [. .. ]
Job am 14.01.2026 bei Jooble gefunden
FERCHAU GmbH
Senior Compliance Specialist Pharma (m/w/d)
• Biberach an der Riß
Abgeschlossenes Studium
Mitarbeiterevents
Dein Aufgabengebiet Du leitest betriebs- und bereichsübergreifende Projekte im
Compliance-Bereich Die Vorbereitung, Planung und Nachbereitung von Audits, Inspektionen und Begehungen gehören zu deinem Aufgabenprofil Du übernimmst die Rolle als [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Investigator für betriebsübergreifende, selbstständige Bearbeitung von Qualitätsereignissen (Abweichungen, OOX) Zu deinen Aufgaben gehört die selbstständige Betreuung verschiedener betriebsübergreifender GMP Fragestellungen, z. B. Risikoanalysen erstellen Du planst betriebsübergreifenden GMP-Schulungen und führst diese durch Du bist zuständig für die Vorstellung von Abweichungen und OOX im Rahmen von Kundenmeetings, Audits und Inspektionen in [. .. ]
Job am 14.01.2026 bei Jooble gefunden
(Senior) Consultant Cybersecurity Technology (m/w/d)
• Köln
Beratungs-/ Consultingtätigkeiten Abgeschlossenes Studium
[. .. ] (OSCP) , Certified Ethical Hacker (CEH) , EC Council Certified Security Analyst (ECSA) , Certified Cyber Forensics Professional (CCFP) , Certified Forensic Computer Examiner (CFCE) und/oder Computer [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Hacking Forensic Investigator (CHFI) , aussagekräftige Berufs- und Projekterfahrung in diesem Umfeld, sehr gute Applikations- und Betriebssystemkenntnisse im Windows-, Linux- und Netzwerkumfeld sowie sehr gute Kenntnisse von Netzwerkprotokollen und Diensten Du rundest dies ab durch: Kenntnisse im Bereich Cloud Security, Kenntnisse im Bereich Mobile Security, Kenntnisse zu standardisierten Empfehlungen wie IT-Grundschutz, ISO 2700x, ISO 25999, Kenntnisse rechtlicher Zusammenhänge zu Compliance-Themen Wissen über verschiedene Angriffsszenarien, Bedrohungen und Hackergruppen, gutes orthografisches und grammatikalisches Ausdrucksvermögen und belastbare Englischkenntnisse in Wort und Schrift. Spricht Dich diese Stelle an? Dann melde Dich bei uns, auch wenn Du nicht zu allen Punkten Ja sagen kannst. Wir würden Dich gerne kennenlernen. Dich erwartet ein regionales Beratungsmodell [. .. ]
Job am 14.01.2026 bei Jooble gefunden
Alexion Pharmaceuticals
Clinical Research Associate
• München
[. .. ] efficient manner on a site level. The CRA acts as the main contact with the study site and has the responsibility for monitoring the study conduct to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] ensure delivery and compliance. The CRA is responsible for the identification, selection, initiation, monitoring and closure of assigned sites in clinical studies, in compliance with Alexion Procedural Documents, international guidelines such as ICH-GCP, and relevant local regulations, and that the sites deliver according to their respective commitment in the individual studies. A CRA [. .. ] Items aging, SDV metrics, Data entry metrics, query aging, MV reports metrics, etc. ) Preparing and finalizing monitoring visit reports in CTMS and provide timely feed-back to the Principal Investigator, including follow-up letter, within required timelines and in line with Alexion SOPs. Ensuring timely collection/ uploading of essential documents into the e TMF in accordance with ICH-GCP, Alexion SOPs and local requirements. Supporting/ participating in regular QC checks of the e TMF In some countries, as required, CRAs are accountable [. .. ]
Job am 14.01.2026 bei Jooble gefunden
Biontech
Manager Medical Science Liaison Oncology
• Berlin
Jobticket
[. .. ] or lung cancer. Support clinical trials by identifying study sites, participating in SIVs (Site Inviations 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 evidence-generation 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. What you have to offer: 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 [. .. ]
Job am 14.01.2026 bei Jooble gefunden
Thermo Fisher Scientific
Local Clinical Trial Manager-FSP, Germany-6 month FTC (m/f/d)
• Homeoffice
[. .. ] required, advises support/ develops and negotiates on contract development with Sites/ CRO/ Vendors ensuring legal input where required and may participate in budget/ contract negotiations with study [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] vendors or clinical investigator sites. As required, selects manages local vendors in accordance with local practices in alignment with overall resourcing strategy for the study; accountable for local vendor management including oversight, agreements, payments, communications issue management. Manages the development of key study documents, plans manuals according to local requirements (monitoring plan, local informed [. .. ] professional skills. As required, assists with audits/ inspections of local clinical operations department and study/ sites in the country (ies) . May act as a point of contact for regulatory/ compliance audits of assigned study (s) ; provides input into LOC and site assessment/ audit proposals and delivers country response follow-up to assessment/ audit reports. Continuously develops and keeps up-to-date knowledge in the areas of GCP, internal company guidelines, SOPs, new monitoring, site, and project management skills and [. .. ]
Neu Job vor 6 Std. bei Jooble gefunden
Alimentiv
Operations Administrator-temp to perm
• Homeoffice
Responsible for the clinical operations of a project within a defined regional/ global level. Provides oversight of project deliverables, assigned Clinical Research Associate (CRAs) and
Investigator sites in accordance [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] with the Monitoring Plan, Protocol, Good Clinical Practice (GCP) , ICH guidelines and local regulations. The COL acts as a primary liaison between the CRAs and the clinical project team. Additional responsibilities include project specific training of CRAs, conducting assessment visits with CRAs, implementation of enrollment and [. .. ] review and track protocol deviations, and support other objectives for clinical operations and the clinical project team. Project Oversight Overall oversight of (a group of) regional CRAs to ensure (site) compliance with study protocol, study plans, ICH-GCP, local regulations and study timelines. Monitoring support visits (Co-monitoring) , per project requirements, to aid the site/ CRA in the satisfactory performance and compliance with standards mentioned above. May support clinical project team by providing oversight of study deliverables related to other [. .. ]
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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 169 offene Stellenanzeigen für Compliance Investigator Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Compliance Investigator Jobs?
Aktuell suchen 37 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:
- Thermo Fisher Scientific (8 Jobs)
- Alimentiv (7 Jobs)
- Alira Health (6 Jobs)
- Incyte Corporation (4 Jobs)
- Helmholtz Association of German Research Centres (4 Jobs)
- Bei Gene (3 Jobs)
In welchen Bundesländern werden die meisten Compliance Investigator Jobs angeboten?
Die meisten Stellenanzeigen für Compliance Investigator Jobs werden derzeit in Bayern (24 Jobs), Nordrhein-Westfalen (13 Jobs) und Hessen (12 Jobs) angeboten.
Zu welchem Berufsfeld gehören Compliance Investigator Jobs?
Compliance Investigator Jobs gehören zum Berufsfeld Compliance & Datenschutz.
