41 Jobs für Financial Investigator
Stellenangebote Financial Investigator Jobs
Job vor 4 Tagen bei StepStone gefunden
Sigmund Freud Privatuniversität Wien
• Wien
[. .. ] researchers and medical specialists. The mission of medical research at SFU is to foster innovation in healthy aging and preventive medicine across all fields of human medicine. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] We actively support investigator-initiated clinical studies and translational research within SFU and its partner hospitals, as well as collaborative projects with external senior scientists, always with the goal of translating research outcomes directly into patient care. Our laboratories are equipped with a broad range of state-of-the-art instruments supporting molecular and [. .. ] SFU MED and in collaboration with national and international partners. Developing biochemical and biomolecular assays to characterize mechanisms of inflammation and disease progression. Acquiring third-party funding and developing sustainable financial plans for expanding research programs. Building and maintaining biobanks and databases of biomaterials and associated metadata for future analyses. Publishing in peer-reviewed journals and representing SFU in international research communities. Developing and supporting interactive, interdisciplinary Ph D programs. Ph D in Biochemistry, Pathophysiology/ Histology, Molecular Biology, or a related field. Demonstrated [. .. ]
Job gestern bei Mindmatch.ai gefunden
Webster Vienna Private University
Assistant/ Associate Professor-Department of Law (f/m/d)
• W wien
Homeoffice möglich
[. .. ] the newly created Department of Law Starting date: Summer 2026 We welcome profiles that strengthen our new department in the following research area: International business law with [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] a focus on financial regulation The following criteria are required: Publications: Produce career stage appropriate academic publications (peer-reviewed journals and books/ book chapters) in line with university research evaluation policies. Third-Party Funding Successfully acquire third-party funding to advance individual research objectives. International visibility (scientific) and cooperation Regularly present papers and research [. .. ] following additional requirements apply: A habilitation or equivalent post-doctoral experience; A distinguished track-record in acquiring and leading externally funded high-level research projects and grants as a Principal Investigator; Experience in supervising Ph D students; Outstanding scientific reputation with internationally recognized peer-reviewed publications and active conferences participation; Proven track record in developing curricula; Demonstrated leadership responsibilities. WVPU supports an attractive environment for ambitious academics. Employment contracts are initially offered for a fixed term of five years. Following a comprehensive [. .. ]
Job am 29.11.2025 bei Mindmatch.ai gefunden
Sigmund Freud Privatuniversität Wien
Professor of Molecular Medicine (m/f/x)
• Vienna
[. .. ] researchers and medical specialists. The mission of medical research at SFU is to foster innovation in healthy aging and preventive medicine across all fields of human medicine. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] We actively support investigator-initiated clinical studies and translational research within SFU and its partner hospitals, as well as collaborative projects with external senior scientists, always with the goal of translating research outcomes directly into patient care. Our laboratories are equipped with a broad range of state-of-the-art instruments supporting molecular and [. .. ] SFU MED and in collaboration with national and international partners. Developing biochemical and biomolecular assays to characterize mechanisms of inflammation and disease progression. Acquiring third-party funding and developing sustainable financial plans for expanding research programs. Building and maintaining biobanks and databases of biomaterials and associated metadata for future analyses. Publishing in peer-reviewed journals and representing SFU in international research communities. Developing and supporting interactive, interdisciplinary Ph D programs. Ph D in Biochemistry, Pathophysiology/ Histology, Molecular Biology, or a related field. Demonstrated [. .. ]
Job am 20.10.2025 bei Jobleads gefunden
Clinical Site Contracts Lead client-based in Munich
• München, Bayern
Führungs-/ Leitungspositionen
[. .. ] the primary point of contact for study teams on all matters related to clinical trial budgets and contracts. Prepare and negotiate site-level grant budgets and Clinical Trial [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Agreements including financial appendices and legal terms. Draft review and manage contract documents using standard templates adapting language as needed in collaboration with Legal. Oversee the end-to-end execution of CTAs Master Agreements and local purchase contracts ensuring alignment with trial timelines. Maintain accurate records in Clinical Trial Management Systems and contract management platforms. Identify and escape business risks appropriately while supporting internal teams with contract-related guidance. Support payment tracking invoice preparation and financial reconciliation for investigator sites as needed. Required Qualifications Bachelors degree in life sciences business or a related field; equivalent experience may be considered. Minimum of 2 years experience negotiating legal and/or financial agreements preferably in clinical research or the pharmaceutical industry. Strong understanding of ICH-GCP guidelines clinical trial start-up processes [. .. ]
Neu Job vor 3 Std. bei Jobleads gefunden
• Wien
[. .. ] and central monitoring deliverables with a focus on patient safety, protocol/ GCP/ regulatory compliance and data integrity. Oversees site interactions post activation through site closeout. This may [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] include patient recruitment, investigator payments or other related activities. May be responsible for identification of critical data and process, protocol execution risks and risk mitigations related to completion of the Risk Assessment and Categorization Tool (RACT) . Reviews the study scope of work, budget and protocol content and ensures the clinical project team (CRAs/ [. .. ] Demonstrated capability of working in an international environment. Demonstrated expertise in site management and monitoring (clinical or central) Preferred experience with risk-based monitoring Demonstrates understanding of clinical trial management financial principles and budget management Knowledge of Good Clinical Practice/ ICH Guidelines and other applicable regulatory requirements Must demonstrate good computer skills Strong conflict resolution skills Demonstrated ability to apply problem solving techniques to resolve complex issues and apply a risk management approach to identifying and mitigating potential threats to the [. .. ]
Job gestern bei Jobleads gefunden
Senior Fraud Investigator (w/m/d)
• München, Bayern
Abgeschlossene Ausbildung
Der Senior Fraud
Investigator ist für alle Aspekte des Ermittlungsprozesses verantwortlich, einschließlich der Erstellung von Ermittlungsplänen, der Identifizierung und Zuweisung relevanter Anfragen, Untersuchungen am Schreibtisch und vor Ort sowie [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] der Berichterstattung über die Ergebnisse. Der Ermittler unterstützt die Schadensachbearbeiter bei der Bearbeitung des Schadensfalls und setzt sein Wissen und seine Erfahrung ein, um sicherzustellen, [. .. ] Antragsteller, Agenten, Makler, Anwälte, medizinische Dienstleister usw. beteiligt sind sowie Durchsetzung angemessener Rechtsmittel auf dem Zivil-oder Strafrechtsweg Tätigkeit in sämtlichen Versicherungssparten mit Schwergewicht Sach-, Haftpflicht- und Personenversicherung sowie Financial Lines und Specialty Unterstützung des Underwriting bei der Überprüfung von Versicherungsbedingungen auf ihre Missbrauchsanfälligkeit sowie bei der Prüfung von zu versichernden Risiken Erhebung von Fakten zu fraglichen Sachverhalten durch offene Befragung und Aufnahme von Aussagen von Zeugen, Arbeitgebern, Anspruchstellern und anderen relevanten Parteien Beschaffung und Sicherung von Beweismitteln zur Unterstützung [. .. ]
Job gestern bei Jobleads gefunden
• Frankfurt (Oder) , Brandenburg
[. .. ] corrective actions are implemented within specified timelines. Identify issues at sites, resolve and escalate as appropriate; collaborate with stakeholders to manage data query resolution for accurate data [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] entry. Ensure the Investigator Folder is up to date and maintain TMFs. Negotiate investigator remuneration, prepare financial contracts, and trigger payments to investigational sites. You will need the following: Right to work in the UK. Up to 2years of pharmaceutical industry experience or other relevant experience (NHS or Academic) . Good knowledge of the drug development process, specifically clinical trial/ research. Knowledge of international standards (GCP/ ICH, [. .. ]
Job vor 5 Tagen bei Jobleads gefunden
Medical Science Liaison NM-Asia Pacific
• Gemeinde Au, Vorarlberg
[. .. ] patients. Generate and execute tactical regional plans to provide needs based, value-added support of the medical and scientific community in line with company goals. Support clinical development [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] initiatives including investigator-initiated research (IIR) and Liva Nova-sponsored clinical studies and registries (e. g. , site identification, trial recruitment, and presentation of final approved data) . Collaborate with key internal and external stakeholders on Medical Affairs-led initiatives including publications, advisory boards, medical education (e. g. , CME) opportunities, training, and [. .. ] Standardization and continuous improvement of medical affairs strategy and procedures across Therapeutic Area (s) Zero discordance of medical affairs activities with strategic plan objectives Job Dimensions Number of associates: TBD Financial responsibility: TBD Impact on the organization: Critical role, determining the strategic direction for Therapeutic Area portfolio (s) Location: Office is home based in Australia Travel: Up to 50 within region Required travel to medical meetings, team meetings, and other group meetings (will require some weekends) Ideal Background: Education: MD in [. .. ]
Job vor 5 Tagen bei Jobleads gefunden
• Köln, Nordrhein- Westfalen Koeln
Führungs-/ Leitungspositionen
[. .. ] Westphalia, Germany Clinical Operations Lead Responsible for the clinical operations of a project within a defined regional/ global level. Provides oversight of project deliverables, assigned Clinical Research [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Associate (CRAs) and Investigator sites in accordance 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 [. .. ] requirements and the monitoring plan Proactive management of site and country performance (recruitment, data collection, document collection, TMF review etc. ) and inform clinical project team on progress Contribute to financial project management processes as applicable. May include but may not be limited to input on revenue recognition, site payments, and site passthrough expense review May be required to manage/ oversee investigator sites including CRA responsibilities, on a temporary or permanent basis Project Liaison Conduct regular global CRA calls with the [. .. ]
Job vor 5 Tagen bei Jobleads gefunden
Clinical Operations Lead
• München, Bayern
Führungs-/ Leitungspositionen
[. .. ] learn more. Base pay range Responsible for the clinical operations of a project within a defined regional/ global level. Provides oversight of project deliverables, assigned Clinical Research [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Associate (CRAs) and Investigator sites in accordance 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 [. .. ] requirements and the monitoring plan Proactive management of site and country performance (recruitment, data collection, document collection, TMF review, etc. ) and inform clinical project team on progress Contribute to financial project management processes as applicable. May include but may not be limited to input on revenue recognition, site payments, and site passthrough expense review May be required to manage/ oversee investigator sites including CRA responsibilities, on a temporary or permanent basis Project Liaison Conduct regular global CRA calls with the [. .. ]
Job vor 5 Tagen bei Jobleads gefunden
Clinical Operations Lead
• Düsseldorf, Nordrhein- Westfalen Duesseldorf
Führungs-/ Leitungspositionen
Clinical Operations Lead 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] sites in accordance 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 [. .. ] requirements and the monitoring plan Proactive management of site and country performance (recruitment, data collection, document collection, TMF review, etc. ) and inform clinical project team on progress Contribute to financial project management processes; may include input on revenue recognition, site payments, and site passthrough expense review May be required to manage/ oversee investigator sites including CRA responsibilities, on a temporary or permanent basis Project Liaison Conduct regular global CRA calls with the monitoring and site management team, as well as [. .. ]
Job vor 8 Tagen bei Jobleads gefunden
Clinical Trial Manager-single sponsor
• München, Bayern
[. .. ] and central monitoring deliverables with a focus on patient safety, protocol/ GCP/ regulatory compliance and data integrity. Oversees site interactions post activation through site closeout. This may [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] include patient recruitment, investigator payments or other related activities. May be responsible for identification of critical data and process, protocol execution risks and risk mitigations related to completion of the Risk Assessment and Categorization Tool (RACT) . Reviews the study scope of work, budget and protocol content and ensures the clinical project team (CRAs/ [. .. ] milestones Demonstrated capability of working in an international environment. Demonstrated expertise in site management and monitoring (clinical or central) Preferred experience with riskbased monitoring Demonstrates understanding of clinical trial management financial principles and budget management Knowledge of Good Clinical Practice/ ICH Guidelines and other applicable regulatory requirements Must demonstrate good computer skills Good communication, presentation and interpersonal skills among project team and with sites Fluency in German Strong conflict resolution skills Demonstrated ability to apply problem solving techniques to resolve complex [. .. ]
Job vor 11 Tagen bei Jobleads gefunden
• Basel, Basel- Stadt
Führungs-/ Leitungspositionen
[. .. ] material. Provides expertise and guidance on initiatives involving processes and systems intended for use in clinical trials to ensure compliance with ICH GCP and any local regulations. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Provide feedback on investigator site performance for future study feasibility purposes. Stays abreast of new and revised government, industry and company regulations, trends and interpretations by participating in trainings, conferences, workshops and discussion groups as appropriate. Core Competencies, Knowledge and Skill Requirements Serves as a GCP expert to the Clinical Operations EMEA with excellent [. .. ] travel Global Competencies Fosters Teamwork Provides and Solicits Honest and Actionable Feedback Self-Awareness Acts Inclusively Demonstrates Initiative Entrepreneurial Mindset Continuous Learning Embraces Change Results-Oriented Analytical Thinking/ Data Analysis Financial Excellence Communicates with Clarity We are proud to be an equal opportunity employer. Be One does not discriminate on the basis of race, religion, color, sex, gender identity, sexual orientation, age, disability, national origin, veteran status or any other basis covered by appropriate law. All employment is decided on the [. .. ]
Job vor 12 Tagen bei Jobleads gefunden
Sponsor Dedicated Study Start Up Lead with Finance expertise based in Munich
• München, Bayern
Führungs-/ Leitungspositionen
[. .. ] Study Start Up Lead with Finance expertise based in Munich We are looking for a sponsor-dedicated Country Start-Up Lead to oversee clinical trial site activation, regulatory processes, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and financial management. This is a well suited role for someone with experience in clinical start-up operations, budget negotiations, and regulatory compliance and who enjoys working collaboratively to drive progress. Key Responsibilities Responsible for execution and oversight of clinical trial country submissions and approvals for assigned protocols. Responsible for managing country deliverables, timelines, and results for assigned protocols to meet country commitments. Work closely with internal and external stakeholders, including sponsors, CROs, and site teams, to streamline processes. Negotiate investigator budgets, oversee financial forecasting, and manage trial-related expenses. Through continual interaction with local clinical team/s successfully delivers clinical and financial contracts within fair market value. Oversight and tracking of clinical research-related payments. Payment reconciliation at study close-out. Qualifications University/ college degree (life science preferred) , or [. .. ]
Job vor 14 Tagen bei Jobleads gefunden
• 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 [. .. ] contracts respectively for : Managing Hospital IEC study submissions and approvals with follow through to ensure successful outcome Preparation of study contracts relevant files to be submitted for the study financial management acceptance, as required by the applicable local legislation Fully explains the purposes, set-up, and procedures of the clinical trial to the Investigators and is responsible for training and assisting them in the conduct of clinical trials Prepares and updates the Clinical Trial Files throughout the study and ensures [. .. ]
Job vor 14 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 [. .. ] contracts respectively for : Managing Hospital IEC study submissions and approvals with follow through to ensure successful outcome Preparation of study contracts relevant files to be submitted for the study financial management acceptance, as required by the applicable local legislation Fully explains the purposes, set-up, and procedures of the clinical trial to the Investigators and is responsible for training and assisting them in the conduct of clinical trials Prepares and updates the Clinical Trial Files throughout the study and ensures [. .. ]
Job am 08.12.2025 bei Jobleads gefunden
Sponsor Dedicated Global Senior Project Manager (CTL level role) remote-Austria
• Wien
[. .. ] and central monitoring deliverables with a focus on patient safety, protocol/ GCP/ regulatory compliance and data integrity. Oversees site interactions post activation through site closeout. This may [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] include patient recruitment, investigator payments or other related activities. May be responsible for identification of critical data and process, protocol execution risks and risk mitigations related to completion of the Risk Assessment and Categorization Tool (RACT) . Reviews the study scope of work, budget and protocol content and ensures the clinical project team (CRAs/ [. .. ] milestones Demonstrated capability of working in an international environment. Demonstrated expertise in site management and monitoring (clinical or central) Preferred experience with riskbased monitoring Demonstrates understanding of clinical trial management financial principles and budget management Knowledge of Good Clinical Practice/ ICH Guidelines and other applicable regulatory requirements Must demonstrate good computer skills Strong conflict resolution skills Demonstrated ability to apply problemsolving techniques to resolve complex issues and apply a risk management approach to identifying and mitigating potential threats to the successful [. .. ]
Job am 05.12.2025 bei Jobleads gefunden
Multi-physic Modelling Research Scientist
• Hamburg
[. .. ] UK SC Security Clearance TRAVEL REQUIRED : Some LOCATION : Filton, Site (60 of your working week must be office based) TYPE : Full time Whats in [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] it for you Financial Reward : Competitive salary, annual profit share, contributory pension, share options, car leasing scheme, free onsite parking, season ticket loan, tax-free technology scheme, shopping discounts and much more Work/ Life Balance : 35 hour week, flexible working around core hours and Friday afternoons off, hybrid working, flexible working Personal [. .. ] 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 28.11.2025 bei Jobleads gefunden
Clinical Operations Lead
• Frankfurt, Hesse
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 [...]
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 [. .. ] requirements and the monitoring plan. Proactive management of site and country performance (recruitment, data collection, document collection, TMF review etc. ) and inform clinical project team on progress. Contribute to financial project management processes as applicable. May include but may not be limited to input on revenue recognition, site payments, and site passthrough expense review. May be required to manage/ oversee investigator sites including CRA responsibilities, on a temporary or permanent basis. Project Liaison Conduct regular global CRA calls with the [. .. ]
Job am 26.11.2025 bei Jobleads gefunden
Professor of Molecular Medicine
• Linz, Oberösterreich
[. .. ] researchers and medical specialists. The mission of medical research at SFU is to foster innovation in healthy aging and preventive medicine across all fields of human medicine. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] We actively support investigator-initiated clinical studies and translational research within SFU and its partner hospitals, as well as collaborative projects with external senior scientists, always with the goal of translating research outcomes directly into patient care. Our laboratories are equipped with a broad range of state-of-theart instruments supporting molecular and cellular [. .. ] within SFU MED and in collaboration with national and international partners. Developing biochemical and biomolecular assays to characterize mechanisms of inflammation and disease progression. Acquiring thirdparty funding and developing sustainable financial plans for expanding research programs. Building and maintaining biobanks and databases of biomaterials and associated metadata for future analyses. Publishing in peerreviewed journals and representing SFU in international research communities. Developing and supporting interactive, interdisciplinary Ph D programs. Your Profile Ph D in Biochemistry, Pathophysiology/ Histology, Molecular Biology, or related field. Demonstrated [. .. ]
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 [. .. ] submissions and contracts respectively for:Managing Hospital IEC study submissions and approvals with follow through to ensure successful outcome Preparation of study contracts relevant files to be submitted for the study financial management acceptance, as required by the applicable local legislation-Fully explains the purposes, set-up, and procedures of the clinical trial to the Investigators and is responsible for training and assisting them in the conduct of clinical trials-Prepares and updates the Clinical Trial Files throughout the study and ensures [. .. ]
Job am 18.11.2025 bei Jobleads gefunden
Clinical Operations Lead
• Stuttgart, Baden- Württemberg
Führungs-/ Leitungspositionen
[. .. ] your recruiter to learn more. Responsible for the clinical operations of a project within a defined regional/ global level. Provides oversight of project deliverables, assigned Clinical Research [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Associate (CRAs) and Investigator sites in accordance 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 [. .. ] requirements and the monitoring plan Proactive management of site and country performance (recruitment, data collection, document collection, TMF review etc. ) and inform clinical project team on progress Contribute to financial project management processes as applicable. May include but may not be limited to input on revenue recognition, site payments, and site pass-through expense review May be required to manage/ oversee investigator sites including CRA responsibilities, on a temporary or permanent basis. Project Liaison Conduct regular global CRA calls with [. .. ]
Job am 18.11.2025 bei Jobleads gefunden
Clinical Operations Lead
• Berlin
Führungs-/ Leitungspositionen
[. .. ] learn more. Base pay range Responsible for the clinical operations of a project within a defined regional/ global level. Provides oversight of project deliverables, assigned Clinical Research [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Associate (CRAs) and Investigator sites in accordance 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 [. .. ] requirements and the monitoring plan. Proactive management of site and country performance (recruitment, data collection, document collection, TMF review, etc. ) and inform clinical project team on progress. Contribute to financial project management processes as applicable. May include but may not be limited to input on revenue recognition, site payments, and site passthrough expense review. May be required to manage/ oversee investigator sites including CRA responsibilities, on a temporary or permanent basis. Project Liaison Conduct regular global CRA calls with the [. .. ]
Job am 08.11.2025 bei Jobleads gefunden
Director, Clinical Study Management
• Frankfurt, Hesse
Führungs-/ Leitungspositionen
[. .. ] term goals and targets. Oversee and/or participate in the project development process working with Sponsors and functional Directors to negotiate and deliver quality product (s) , assessing [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] resource and financial and safety requirements, assigning resources, overseeing trial conduct, information, and data confidentiality, and supporting project teams by assisting the troubleshooting and resolution process while ensuring all align with corporate objectives. Responsible to ensure sufficient project level staffing and maintain utilization targets. Represent project operations on cross-department planning initiatives. Unit [. .. ] of project operations team at client meetings. Represent project operations at business development meetings including but not limited to bid defenses, general capabilities, and scientific conferences. Attend and present at investigator meetings as needed. Product Service/ Excellence (10-15) Works in collaboration with leadership team to achieve excellence in project services, evaluating and implementing recommendations to minimize organizational risk, meet all regulatory and/or industry standards, while creating and promoting programs that support the Organizations growth as a world class provider [. .. ]
Job am 08.11.2025 bei Jobleads gefunden
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 [...]
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 [. .. ] requirements and the monitoring plan. Proactive management of site and country performance (recruitment, data collection, document collection, TMF review etc. ) and inform clinical project team on progress. Contribute to financial project management processes as applicable. May include but may not be limited to input on revenue recognition, site payments, and site pass-through expense review. May be required to manage/ oversee investigator sites including CRA responsibilities, on a temporary or permanent basis. Project Liaison Conduct regular global CRA calls with [. .. ]
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Häufig gestellte Fragen
Wieviel verdient man als Financial investigator pro Jahr?
Als Financial investigator verdient man zwischen EUR 50.000,- bis EUR 80.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Financial Investigator Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 41 offene Stellenanzeigen für Financial Investigator Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Financial Investigator Jobs?
Aktuell suchen 6 Unternehmen nach Bewerbern für Financial Investigator Jobs.
Welche Unternehmen suchen nach Bewerbern für Financial Investigator Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Financial Investigator Stellenangebote:
- Veeda Lifesciences (11 Jobs)
- Webster Vienna Private University (1 Job)
- European Central Bank (1 Job)
- Bei Gene (1 Job)
In welchen Bundesländern werden die meisten Financial Investigator Jobs angeboten?
Die meisten Stellenanzeigen für Financial Investigator Jobs werden derzeit in Nordrhein-Westfalen (8 Jobs), Niedersachsen (5 Jobs) und Bayern (5 Jobs) angeboten.
Zu welchem Berufsfeld gehören Financial Investigator Jobs?
Financial Investigator Jobs gehören zum Berufsfeld Finanzwesen.
