39 Jobs für Financial Investigator
Stellenangebote Financial Investigator Jobs
Job vor 2 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 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
• 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 [. .. ]
Job vor 3 Tagen bei Jobleads gefunden
Clinical Operations Lead
• 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 3 Tagen bei Jobleads gefunden
• 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 3 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 3 Tagen bei Jobleads gefunden
• 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 6 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 9 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 10 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 12 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 12 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 vor 14 Tagen 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/ [. .. ] 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
• 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 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 10.11.2025 bei Jobleads gefunden
Contract Specialist-hybrid in Munich
• München, Bayern
[. .. ] and driven to accelerate the delivery of therapies because we are passionate about changing lives. Job Responsibilities Administers all contract management processes, including coordination with relevant protocol, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] informed consent, institution, investigator, vendor, consultant, and customer agreement documents at a project level. May lead (with supervision) multicountry projects including negotiating and preparing contracts, budgets, and related documents for participation in industrysponsored clinical trials. Provides support to SSUL to agree on country template contract and budget. Produces sitespecific contracts from country template. Provides [. .. ] contracts staff and internal and external customers. Provides functional guidance and keeps internal and external teams aware of all contract statuses or pending issues. Prepares correspondence as necessary. Monitors basic financial aspects of the project and the number of hours/ tasks available per contract; escalates discrepancies in a timely fashion. Reviews and complies with Standard Operating Procedures (SOPs) and Work Instructions (WIs) in a timely manner, keeps training records updated accordingly and ensures timesheet compliance. Qualifications BA/ BS degree in Business [. .. ]
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 [. .. ]
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 15.10.2025 bei Jobleads gefunden
Clinical Site Contracts Lead client-based in Munich
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 escalate 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, [. .. ]
Job am 09.10.2025 bei Jobleads gefunden
Clinical Operations Lead
• Frankfurt, Hesse
Führungs-/ Leitungspositionen
Responsibilities 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 22.08.2025 bei Jobleads gefunden
Director, Imaging Project Management
• Köln, Nordrhein- Westfalen
Führungs-/ Leitungspositionen
[. .. ] allocation, resource planning, project oversight, training and development, employee engagement, team building, performance management, and succession planning. Represents the imaging project management function as a senior leader [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] in client meetings, investigator sessions, and business development engagements, reinforcing a culture of excellence, partnership, and customer focus. Project and Product Leadership (10-15) Provides strategic oversight and direct involvement in imaging project development, collaborating with Sponsors and functional Directors to negotiate scope, allocate resources, and ensure delivery of high-quality, compliant solutions. Oversees [. .. ] world-class provider of medical imaging services. Contributes to the research and design of new products, overseeing operational implementation and maintaining an emphasis on risk management throughout the product lifecycle. Financial Strategy and Risk Management (10-15) Partners with medical imaging leadership to lead strategic budget planning, advocacy, and performance reporting during annual and operational review cycles, ensuring alignment with organizational goals and financial targets. Oversees the development and application of tools and methodologies to track and manage project and departmental [. .. ]
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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 39 offene Stellenanzeigen für Financial Investigator Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Financial Investigator Jobs?
Aktuell suchen 5 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)
- 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), Bayern (5 Jobs) und Niedersachsen (5 Jobs) angeboten.
Zu welchem Berufsfeld gehören Financial Investigator Jobs?
Financial Investigator Jobs gehören zum Berufsfeld Finanzwesen.
