UNKNOWN

FEED

REQUIREMENTS: Previous Experience: Demonstrated proficiency in covert surveillance techniques, capturing high-quality video footage, and preparing thorough, well-organized investigative reports. This role involves performing both stationary and mobile surveillance, obtaining video and photographic evidence, and preparing thorough, detailed reports for clients.

Ethos Risk Services LLC

Investigator

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When you join Guerbet, you: Are choosing a global leader with recognized expertise in diagnostic and interventional imaging, Are joining our 2820 collaborators who are committed every day to offering innovative solutions to improve quality of patient's life all over the world, Are joining a company where we value diversity of talents coming from various horizon. Assist in the department in trending of metrics (i.e., Cost of Poor Quality, Key Performance Indicators, Quality Management Reviews, & Data Trend Analysis).

Guerbet SA

Responsibilities: of the Threat Hunter Investigator: Conduct proactive threat hunting and insider threat investigations leveraging logs, endpoint data, user activity, and behavioral analytics. Create technical documentation, runbooks, and detection content while continuously improving alert quality and coverage aligned to MITRE ATT&CK.

YEAR

Zp Group Llc

Threat Hunter Investigator - 177302 - 177697

Additional responsibilities will include developing an investigative plan for complaints and incident reports, contacting all involved parties, and providing them with information about the investigative process, ensuring a well-documented investigation, analyzing information and working with the appropriate University offices in the course of investigations, maintaining accurate and thorough investigatory files and reports, providing on-going updates to the office leadership, as necessary, presenting the investigative record and/or determination in hearings or grievance proceedings, and continuously identifying and integrating best practices in investigations. Department University Compliance Office-263000 Career Area Other Posting Open Date 10/08/2026 Application Deadline 10/29/2026 Open Until Filled No Position Type Permanent Staff (EHRA NF) Working Title Compliance Investigator Appointment Type EHRA Non-Faculty Position Number 20020623, 01004808 Vacancy ID NF0010106 Full Time/Part Time Full-Time Permanent FTE 1 Hours per week 40 Position Location North Carolina, US Hiring Range $85,000 - $96,394 Proposed Start Date 12/07/2026.

The University of North Carolina at Chapel Hill is an equal opportunity and affirmative action employer. All qualified applicants will receive consideration for employment without regard to age, color, disability, gender, gender expression, gender identity, genetic information, national origin, race, religion, sex, sexual orientation, or status as a protected veteran.

University of North Carolina at Chapel Hill

Compliance Investigator

GUERBET

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When you join Guerbet, you: Are choosing a global leader with recognized expertise in diagnostic and interventional imaging, Are joining our 3000 collaborators who are committed every day to offering innovative solutions to improve quality of patient's life all over the world, Are joining a company where we value diversity of talents coming from various horizons. Cognitive Requirements: The position routinely interfaces with various personnel from all site departments (Operations, M&D, Engineering, QC and QA), as well as corporate personnel and external suppliers.

Principal Investigator

Composed of more than 2,600 faculty physicians and researchers, nearly 2,000 students, and more than 6,200 staff, the Duke University School of Medicine along with the Duke University School of Nursing, and Duke University Health System comprise Duke Health, a world-class academic medical center. The ideal candidate will have relevant knowledge and industrial experience in the field of bioprocess development for manufacture of cellular and tissue-based therapies and will have experience transferring processes to cGMP facilities for clinical or commercial manufacture.

Duke University

GMP Compliance Investigator - Equipment And Facilities - Marcus Center For Cellular Cures

GMP Compliance Investigator - Equipment and Facilities - Marcus Center for Cellular Cures

The field-based Health Economics & Outcomes Research (HEOR) Science Liaison is a scientifically trained, field-based expert, that serves as the interface between the company and external healthcare decision makers (HCDMs), including managed care organizations, pharmacy benefit managers, and other health technology assessment bodies. The HEOR Science Liaison delivers credible, non-promotional scientific information across clinical evidence, real-world evidence (RWE), pharmacoeconomic information, and health outcomes to support informed formulary, coverage, and reimbursement decisions.

Compass Pathways

Director, Field HEOR

GreenHouseAPI

MSL) will prioritize contacts with key opinion leaders (KOLs), healthcare providers, and clinical investigators within an assigned U.S. region, providing scientific exchange and supporting the generation of actionable insights. MSL is expected to deliver scientifically accurate, relevant, and increasingly insightful discussions, gather and communicate insights from the field, and support execution of regional priorities.

Celldex Therapeutics Inc

Senior Manager, Field Medical Science Liaison, Carolinas

Assist Clinical Project Manager / Director or Clinical Research Manager / Clinical Operations Director with preparing data reports for site and Clinical Research Associate (CRA) management; provide support for site management activities. Prepare initial drafts, including templates and content, of internal reports, external reports, newsletters, and other clinical project communications; distribute reports and communications to sites, vendors, Sponsors, and internal team members.

Join The CTI Team

Clinical Project Coordinator

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Job Summary: Labcorp is seeking a Senior Lead Biostatistician to join our cross-functional Evidence Generation team, supporting a growing portfolio of oncology research initiatives, with a focus on observational clinical validity studies in minimal residual disease (MRD), alongside investigator-initiated studies, registries, and real-world evidence programs. Independently perform statistical analyses across diverse datasets (clinical, assay/validation, and real-world/registry data) using appropriate methods (e.g., regression, survival analysis, validation approaches), ensuring accuracy, reproducibility, and appropriate documentation.

LabCorp

Sr. Lead Biostatistician - Oncology Evidence Generation

FULL_TIME

Strong experience with development and writing of nonclinical documents (eg, Module 2.4 and 2.6 eCTD submission documents, 1st Edition Investigator’s Brochure [IB], Nonclinical Study Reports, Meeting Requests, Briefing Documents, RTQs). With a global footprint across four continents, MMS not only maintains an industry-leading customer satisfaction rating but also fosters a collaborative and inclusive work environment where employees can thrive.

Senior Nonclinical Writer (US)

partner JazzHR

Lead CRA, if assigned) Oversee monitoring on complex studies; develop study-specific monitoring documents (e.g., CMP, deviation plan, report templates); finalize visit reports; train/coordinate CRAs; act as primary clinical monitoring contact for PM/Sponsor and handle CRA escalations. Through end-to-end clinical trial delivery, home health services, expanded access programs, and market access consultancy, we provide flexible, fit-for-purpose solutions that support drug development, improve access, and help therapies reach the right patients at the right time.

WEP Clinical

Senior Clinical Research Associate

Labcorp is seeking a Senior Lead Biostatistician to join our cross-functional Evidence Generation team, supporting a growing portfolio of oncology research initiatives, with a focus on observational clinical validity studies in minimal residual disease (MRD), alongside investigator-initiated studies, registries, and real-world evidence programs. Independently perform statistical analyses across diverse datasets (clinical, assay/validation, and real-world/registry data) using appropriate methods (e.g., regression, survival analysis, validation approaches), ensuring accuracy, reproducibility, and appropriate documentation.

Labcorp

Conduct audits of designated studies and facilities to assess compliance with protocols, SOPs, methods and relevant regulations (audits may include direct observation of study conduct and/or laboratory processes, review of protocols, study data and reports, or review of facility records and SOPs as well as subcontractor contributions). As a leading global contract research organization (CRO), we partner with researchers to tackle complex scientific challenges, drive innovation, and help build a healthier, safer world.

Field Investigator Jobs in Durham, NC

Investigator Ethos Risk Services LLC

Investigator Guerbet SA

Threat Hunter Investigator - 177302 - 177697 Zp Group Llc

Compliance Investigator University of North Carolina at Chapel Hill

Investigator GUERBET

Principal Investigator GUERBET

GMP Compliance Investigator - Equipment And Facilities - Marcus Center For Cellular Cures Duke University

GMP Compliance Investigator - Equipment and Facilities - Marcus Center for Cellular Cures Duke University

Director, Field HEOR Compass Pathways

Senior Manager, Field Medical Science Liaison, Carolinas Celldex Therapeutics Inc

Clinical Project Coordinator Join The CTI Team

Sr. Lead Biostatistician - Oncology Evidence Generation LabCorp

Senior Nonclinical Writer (US) MMS

Senior Clinical Research Associate WEP Clinical

Sr. Lead Biostatistician - Oncology Evidence Generation Labcorp

Quality Assurance Auditor I Inotiv, Inc

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