OTHER

FEED

UNKNOWN

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.

ABOUT US: Ethos Risk Services is a leading insurance claims investigation and medical management company, specializing in surveillance and fraud detection. At the forefront, we provide accurate data and actionable insights that translate into better decision-making for our clients. JOB SUMMARY:Our dynamic Ethos team is seeking an Experienced Field Investigator to conduct surveillance and investigative activities to identify potential fraudulent insurance claims. This role involves performing both stationary and mobile surveillance, obtaining video and photographic evidence, and preparing thorough, detailed reports for clients. KEY RESPONSIBILITIES:<ul><li>Case Preparation: Prepare for surveillance assignment by reviewing Ethos' preliminary reports and case information.</li><li>Field Surveillance: Perform covert surveillance from your vehicle by tracking and capturing high-quality video evidence of surveillance targets.</li><li>Report Writing: Draft detailed and court-ready investigative reports summarizing activity and key findings.</li><li>Documentation: Finalize case file by submitting case reports and uploading video footage via personal laptop at the end of the day.</li><li>Communication: Work closely with the field supervisor and operations teams, receiving regular guidance and mentorship.</li></ul> REQUIREMENTS:<ul><li>Previous Experience: Demonstrated proficiency in covert surveillance techniques, capturing high-quality video footage, and preparing thorough, well-organized investigative reports.</li><li>Driver's License: Valid driver's license and proof of automobile insurance.</li><li>Personal Vehicle: A well-maintained vehicle that is always reliable (preferably with tinted windows).</li><li>Surveillance Equipment: A handheld camcorder with high-quality zoom and a covert camera device. Use of stabilization equipment (gimbals, tripods, etc.) is strongly encouraged.</li><li>Technology: A reliable laptop, cell phone, and internet service are needed for communication and administrative tasks.</li><li>Private Investigator License: Active Private Investigator license or willingness to obtain one (where required by state).</li></ul> WORKING CONDITIONS:<ul><li>While we aim to keep assignments within a 2-hour drive of your residence, occasional further travel and overnight stays (covered by the company) may be required</li><li>Most surveillance cases start at 6:00AM. End time can vary depending on activity and a typical workday can vary from 3-12 hours.</li><li>Weekends/holidays are common workdays as claimants are more likely to be active.</li><li>This is an independent role often requiring long hours alone in your vehicle, regardless of weather conditions.</li><li>Must remain alert with no external distractions, ready to use videography equipment to document subjects.</li></ul> Ethos Risk Services is an equal opportunity employer that does not discriminate on the basis of religious creed, sex, national origin, race, veteran status, disability, age, marital status, color or sexual orientation or any other characteristic. A background check will be conducted, in accordance to the local state law and regulations. Job Posted by ApplicantPro

Ethos Risk Services

Investigator

Administrative Skills

Auto Insurance

Cellular Telephone

Driver's License

Insurance Claims

Internet/Online Service

Investigative Reports

Laptop PC

Mentoring

Mobile Devices

Operations Management

Organizational Skills

Reporting Skills

Risk

Surveillance

Willing to Travel

Talent Acquisition

FULL_TIME

YEAR

Our purpose is bold: to bring clinical trials front and center in your community, make them accessible to everyday people, and empower underrepresented communities to participate. At Civia Health, we’re reimagining how clinical trials are delivered—by putting patients first and empowering providers to lead innovation.

Reports to: Medical Director Join Us at Civia Health At Civia Health, we’re reimagining how clinical trials are delivered—by putting patients first and empowering providers to lead innovation. We’re seeking an experienced and compassionate Principal Investigator (PI) to oversee Phase 2–4 clinical trials in a collaborative, mission-driven environment. You’ll play a vital role in ensuring scientific integrity, patient safety, and regulatory compliance while contributing to groundbreaking research. At Civia Health, you're not just taking a job: You're joining a mission to transform the way clinical research is done. Our purpose is bold: to bring clinical trials front and center in your community, make them accessible to everyday people, and empower underrepresented communities to participate. We’re reinventing how clinical studies are run, delivering valid, scalable evidence with a consumer-first mindset. Too often, trials are expensive, fragmented, and overlook the experience of the participant. At Civia, we’re changing that. Our leadership team are experienced industry leading, visionary professionals who know what’s broken — and how to fix it. We treat participants like valued partners, not research subjects. That means supporting their agency, putting their needs, comfort, and enjoyment first — and rewarding them generously for their time and effort. What It Means to Work at Civia Every team member plays a crucial role in reshaping clinical research. You’ll help make studies more human-centered, inclusive, and efficient. We're looking for people who are driven by purpose, inspired by innovation, and ready to roll up their sleeves to do meaningful work.   At Civia, your contributions aren’t just transactional, they’re transformational. What You’ll Do <ul><li>Serve as the physician of record and lead clinical oversight for assigned trials. </li></ul><ul><li>Review and approve study protocols, informed consent documents, and source documentation. </li></ul><ul><li>Conduct physical exams, medical reviews, and oversee safety assessments for participants. </li></ul><ul><li>Ensure compliance with all ICH-GCP, FDA, and IRB regulations. </li></ul><ul><li>Provide guidance and mentorship to the clinical research team. </li></ul><ul><li>Engage with sponsors, monitors, and regulatory bodies as needed. </li></ul><ul><li>Occasional travel may be required for audits, site visits, or team meetings.  </li></ul>What You Bring <ul><li>Medical degree (MD or DO) with active and unrestricted license. </li></ul><ul><li>3+ years of experience as a Principal Investigator in clinical research (Phase 2–4 preferred). </li></ul><ul><li>Board certification in internal medicine, endocrinology, or related field preferred. </li></ul><ul><li>Strong working knowledge of GCP, FDA regulations, and clinical operations. </li></ul><ul><li>Excellent leadership, communication, and problem-solving skills. </li></ul><ul><li>Passion for innovation, ethics, and patient-centered care. </li></ul>What We Offer <ul><li>Competitive compensation </li></ul><ul><li>Medical, dental, and vision insurance </li></ul><ul><li>Generous PTO and paid holidays </li></ul><ul><li>Flexible scheduling options </li></ul><ul><li>Professional development and continuing education support </li></ul><ul><li>A mission-driven team that values respect, inclusion, and innovation </li></ul>Ready to Make an Impact? <ul><li>Mission with Meaning: Be part of a purpose-led team committed to health equity and real-world impact. </li></ul><ul><li>Startup Energy, Proven Expertise: Work fast, adapt quickly, and help build something new; guided by seasoned visionary professionals who’ve seen what needs to change. </li></ul><ul><li>People First Culture: We care deeply about our patients, participants, and each other. Collaboration, transparency, and bold, straight-talking are core to how we work. </li></ul><ul><li>Invested in Your Growth: We don’t just hire for today; we’re building the leaders and changemakers of tomorrow.  </li></ul>If you’re ready to be part of something meaningful—and work with people who care deeply about doing good work—apply today by submitting your resume and cover letter to the link above. We’re excited to learn more about you! Powered by JazzHR

Civia Health

Principal Investigator, MD

Clinical Monitoring

Clinical Research

Clinical Trial

Communication Skills

Dental Insurance

Endocrinology

FDA Requirements

GCP (Good Clinical Practices)

ICH Regulations

IRB/IEC (Institutional Review Board/Independent Ethics Committee)

Internal Medicine

Leadership

Maintain Compliance

Medical Records

Monitor Regulations

Patient Safety

People Management

Phase II Clinical Trials

Phase IV Clinical Trials

Problem Solving Skills

Quality of Care

Regulatory Compliance

Startup

Team Lead/Manager

Team Player

Vision Plan

partner JazzHR

CONTRACTOR

Position Summary: The Institute for Trauma Recovery at the Client is looking for a data analyst/statistician at or above the master’s degree level, to work in a collaborative team of investigators and perform statistical analyses to Product new discoveries to help trauma survivors. CUSTOM FIELDS: Work Location: Hybrid Onsite/Hybrid Parking: Parking Available Minimum Years of Experience Required: 3 Minimum Years of Education After High School Required: 8

Job Title: Statistician Investigator Location: Chapel Hill, NC 27516 Duration: 6 Months+ (possibility of extension) Note: The hybrid schedule is Monday, Tuesday, Wednesday in the office, remote Thursday and Friday. Cover letter is required along with resume. Please include in submittal. Position Summary: The Institute for Trauma Recovery at the Client is looking for a data analyst/statistician at or above the master’s degree level, to work in a collaborative team of investigators and perform statistical analyses to Product new discoveries to help trauma survivors. The primary focus of the position will be to assist with analyses of diverse longitudinal data collected as part of the Client million dollar AURORA study. This study, funded by the National Institute of Mental Health and private and foundation partners, enrolled individuals presenting to a large network of emergency departments in the immediate aftermath of trauma. Study participants were followed longitudinally for one year, beginning in the hours after trauma, using sophisticated adaptive sampling methods and state-of-the-art battery of self-report, neurocognitive, physiologic, digital phenotype, psychosocial, neuroimaging, and genomic markers. In addition to analyses of these data, the statistician will also analyze data from longitudinal data collected as part of many other past and current R01 studies going on in the institute, as well as the analysis of clinical trial data. Required Qualifications, Competencies and Experience: Strong organizational skills. Must be able to analyze diverse longitudinal data collected as part of research studies. Must have prior experience publishing peer-reviewed manuscripts. Must have experience preparing other academic, grant, or stakeholder-facing materials. Preferred Qualifications, Competencies, and Experience: Ideal candidates would have experience with software and the ability to collaborate effectively in a multidisciplinary environment. Prior with advanced statistical methods (e.g., multilevel modeling, latent/class cluster analysis, regression-based methods) is preferred, as is familiarity with machine learning techniques. Candidates should also demonstrate proficiency with both basic and advanced statistical analyses in clinical or epidemiological research. Minimum of a relevant Master’s degree (or foreign degree equivalent) preferred. Ideal candidates will have a PhD in a social, applied, or related science discipline. Demonstrated ability as a scientific writer. Demonstrated ability to perform advanced statistical analyses and learn and perform statistical analyses new to them. Expert knowledge of R and other software packages. Ability to collaborate effectively on multidisciplinary teams. Master’s degree with extensive experience will be considered. Description of Work: Data analysis. Develop scripts/code as necessary to streamline/optimize analyses. Communication – writing/editing. Writing and contributing to peer-reviewed publications. Writing results reports and presenting findings in stakeholder meetings or research conferences. Data Collection. Assist with analyses of diverse longitudinal data collected as part of the AURORA study. Administration. Maintaining meta-data regarding databases and work performed. Other. Developing analysis plans in collaboration with members of the research team. CUSTOM FIELDS: Work Location: Hybrid Onsite/Hybrid Parking: Parking Available Minimum Years of Experience Required: 3 Minimum Years of Education After High School Required: 8

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Investigator Jobs in Caldwell, NC

Investigator Ethos Risk Services

Principal Investigator, MD Civia Health

Statistician Investigator Integrated Resources, Inc

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