FULL_TIME

FEED

YEAR

We’re looking for a compassionate and experienced Nurse Practitioner to support our clinical research team in conducting Phase 2–4 trials, with a particular focus on metabolic conditions and GLP-1 therapies. 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.

Job Type: Full-time, on-siteReports to: Director, Site Management  Join Us at Civia Health   We’re looking for a compassionate and experienced Nurse Practitioner to support our clinical research team in conducting Phase 2–4 trials, with a particular focus on metabolic conditions and GLP-1 therapies. If you thrive in a collaborative, patient-centered environment and are passionate about research-driven care, we’d love to meet you. 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>Conduct study visits including medical assessments, physical exams, and protocol-specific procedures. </li></ul><ul><li>Partner with principal investigators and research staff to ensure quality, safety, and regulatory compliance. </li></ul><ul><li>Engage participants with empathy—providing clear education, answering questions, and ensuring comfort throughout the trial process. </li></ul><ul><li>Identify, document, and report adverse events per protocol and regulatory standards. </li></ul><ul><li>Maintain accurate, timely, and high-quality documentation in source records and EDC systems. </li></ul><ul><li>Contribute to continuous improvement of workflows and study execution with a team-first mindset. </li></ul><ul><li>Occasional travel may be required for audits, site visits, or team meetings.  </li></ul>What You Bring <ul><li>Active, unrestricted Nurse Practitioner license or Physician's Assistant license. </li></ul><ul><li>2+ years of clinical research experience (Phase 2–4 trials preferred). </li></ul><ul><li>Experience with GLP-1 therapies or metabolic/endocrine research highly preferred. </li></ul><ul><li>Strong knowledge of GCP/ICH guidelines; certification is a plus. </li></ul><ul><li>Excellent clinical judgment, attention to detail, and communication skills. </li></ul><ul><li>A collaborative spirit and commitment to doing what’s best for the patient and the team. </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

Nurse Practitioner/Sub-Investigator

Clinical Research

Clinical Trial

Communication Skills

Conduct Studies

Continuous Improvement

Dental Insurance

Detail Oriented

GCP (Good Clinical Practices)

GLP (Good Laboratory Practices)

Leadership

Medical Treatment

Nurse Practitioner

Nursing Credentials

Phase II Clinical Trials

Phase IV Clinical Trials

Physician Assistant

Physician Credential

Regulatory Compliance

Research Skills

Safety Compliance

Startup

Team Lead/Manager

Team Player

Training/Teaching

Vision Plan

partner JazzHR

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

Principal Investigator, MD

Clinical Monitoring

Endocrinology

FDA Requirements

ICH Regulations

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

Internal Medicine

Maintain Compliance

Medical Records

Mentoring

Monitor Regulations

Patient Safety

People Management

Problem Solving Skills

Quality of Care

OTHER

UNKNOWN

Overview:
Company Overview: Advance Your Career in Insurance Claims with Allied Universal® Compliance and Investigation Services. Allied Universal® Compliance and Investigation Services is the premier destination for a career in insurance claim investigation. As a global leader, we provide dynamic opportunities for claim investigators, SIU investigators, and surveillance investigators. Our team is committed to innovation and excellence, making a significant impact in the insurance industry. If you’re ready to grow with the best, explore a career with us and make a difference.

Job Description:
Allied Universal® is hiring a Surveillance Investigator. The Surveillance Investigator will perform discreet mobile and stationary surveillance of a Claimant to confirm current activities and capabilities to assist with the administration of an insurance claim. <ul style="margin: 0px; padding: 0px; font-family: verdana;"><li style="margin: 0px 0px 0px 22px; padding: 0px; font-size: 10pt; font-family: Verdana, Verdana_MSFontService, sans-serif;" aria-setsize="-1" data-leveltext="" data-font="Symbol" data-listid="15" data-list-defn-props="{"335552541":1,"335559685":1440,"335559991":360,"469769226":"Symbol","469769242":[8226],"469777803":"left","469777804":"","469777815":"hybridMultilevel"}" data-aria-posinset="29" data-aria-level="1">Pay Rate: starting at $23 / hr<span style="margin: 0px; padding: 0px; font-size: 10pt; font-family: Verdana, Verdana_EmbeddedFont, Verdana_MSFontService, sans-serif;" data-ccp-props="{"134233117":false,"134233118":false,"201341983":0,"335559685":700,"335559737":-20,"335559738":0,"335559739":0,"335559740":279}"> </li></ul><ul style="margin: 0px; padding: 0px; font-family: verdana;"><li style="margin: 0px 0px 0px 22px; padding: 0px; font-size: 10pt; font-family: Verdana, Verdana_MSFontService, sans-serif;" aria-setsize="-1" data-leveltext="" data-font="Symbol" data-listid="15" data-list-defn-props="{"335552541":1,"335559685":1440,"335559991":360,"469769226":"Symbol","469769242":[8226],"469777803":"left","469777804":"","469777815":"hybridMultilevel"}" data-aria-posinset="30" data-aria-level="1">Private Investigator’s license required prior to applying<span style="margin: 0px; padding: 0px; font-size: 10pt; font-family: Verdana, Verdana_EmbeddedFont, Verdana_MSFontService, sans-serif; color: #2d2d2d;" data-ccp-props="{"134233117":false,"134233118":false,"201341983":0,"335559685":700,"335559737":-20,"335559738":0,"335559739":0,"335559740":279}"> </li></ul><ul style="margin: 0px; padding: 0px; font-family: verdana;"><li style="margin: 0px 0px 0px 22px; padding: 0px; font-size: 10pt; font-family: Verdana, Verdana_MSFontService, sans-serif;" aria-setsize="-1" data-leveltext="" data-font="Symbol" data-listid="15" data-list-defn-props="{"335552541":1,"335559685":1440,"335559991":360,"469769226":"Symbol","469769242":[8226],"469777803":"left","469777804":"","469777815":"hybridMultilevel"}" data-aria-posinset="31" data-aria-level="1">Must possess a valid driver's license with at least one year of driving experience<span style="margin: 0px; padding: 0px; font-size: 10pt; font-family: Verdana, Verdana_EmbeddedFont, Verdana_MSFontService, sans-serif; color: #333333;" data-ccp-props="{"134233117":false,"134233118":false,"201341983":0,"335559685":700,"335559737":-20,"335559738":0,"335559739":0,"335559740":279}"> </li></ul> RESPONSIBILITIES:<ul><li>Conduct independent investigations of insurance claims across a range of coverage types, including workers’ compensation, general liability, property and casualty, and disability</li><li>Utilize various surveillance techniques and equipment to monitor subjects covertly</li><li>Document and report observations, activities, and any relevant information in a clear and concise manner</li><li>Collaborate with other investigators and law enforcement agencies as needed to gather information and coordinate efforts</li><li>Maintain confidentiality and adhere to legal and ethical standards in conducting surveillance operations</li></ul>QUALIFICATIONS (MUST HAVE):<ul><li>High school diploma or equivalent</li><li>Post offer, must be able to successfully complete the Allied Universal Investigations' training/orientation course</li><li>Minimum of one (1) year of verifiable work experience, preferably involving investigations or other protective service-related field</li><li>Flexibility to work varied and irregular hours/days including weekends and holidays</li><li>Ability to type reports in Microsoft Word format with minimal grammatical and punctuation errors</li><li>Proficient in utilizing laptop computers, video cameras and cell phones</li><li>Capable of maintaining focus and multitasking effectively in a dynamic environment</li><li>Demonstrated ability to manage stressful situations with composure and professionalism</li><li>Ability to work in a very independent environment</li></ul>PREFERRED QUALIFICATIONS (NICE TO HAVE):<ul><li>Associate’s Degree or higher, preferably in Criminal Justice</li><li>Security/Loss Prevention experience</li><li>Military experience</li><li>Law enforcement experience</li><li>Prior insurance investigations experience</li><li>Prior educational or professional incident reporting and/or investigations experience</li></ul>BENEFITS:<ul><li>Medical, dental, vision, basic life, AD&D, retirement plan and disability insurance</li><li>Seven paid holidays annually, sick days available where required by law</li><li>Vacation time offered at an initial accrual rate of 3.08 hours biweekly; unused vacation is only paid out where required by law</li></ul>

Closing:
Allied Universal® is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race/ethnicity, age, color, religion, sex, sexual orientation, gender identity, national origin, genetic information, disability, protected veteran status or relationship/association with a protected veteran, or any other basis or characteristic protected by law. For more information: www.aus.com If you have difficulty using the online system and require an alternate method to apply or require an accommodation, please contact our local Human Resources department. To find an office near you, please visit: www.aus.com/offices.

Requisition ID:
2026-1602469

Allied Universal provides unparalleled service, systems and solutions to the people and business of our communities, and is North America's leading security services provider. With over 140,000 employees, Allied Universal delivers high-quality, tailored solutions, which allows clients to focus on their core business. For more information: 866.825.5433 or <a href="http://www.aus.com/" target="_blank">www.AUS.com</a>

Investigator Jobs in Gladstone, MO

Resume Resources

Get noticed by top employers!

Investigator Jobs in Gladstone, MO

Nurse Practitioner/Sub-Investigator Civia Health

Principal Investigator, MD Civia Health

Surveillance Investigator Allied Universal

Resume Resources