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Civia health
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  • Nurse Practitioner/Sub-Investigator  

    - Saint Louis
    Job DescriptionJob DescriptionJob Type: on-siteReports to: Medical Dir... Read More
    Job DescriptionJob Description

    Job Type: on-site

    Reports to: Medical Director 
     

    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 

    Conduct study visits including medical assessments, physical exams, and protocol-specific procedures. 

    Partner with principal investigators and research staff to ensure quality, safety, and regulatory compliance. 

    Engage participants with empathy—providing clear education, answering questions, and ensuring comfort throughout the trial process. 

    Identify, document, and report adverse events per protocol and regulatory standards. 

    Maintain accurate, timely, and high-quality documentation in source records and EDC systems. 

    Contribute to continuous improvement of workflows and study execution with a team-first mindset. 

    Occasional travel may be required for audits, site visits, or team meetings.  

    What You Bring 

    Active, unrestricted Nurse Practitioner license in Missouri. 

    2+ years of clinical research experience (Phase 2–4 trials preferred). 

    Experience with GLP-1 therapies or metabolic/endocrine research highly preferred. 

    Strong knowledge of GCP/ICH guidelines; certification is a plus. 

    Excellent clinical judgment, attention to detail, and communication skills. 

    A collaborative spirit and commitment to doing what’s best for the patient and the team. 

    What We Offer 

    Competitive compensation 

    Medical, dental, and vision insurance 

    Generous PTO and paid holidays 

    Flexible scheduling options 

    Professional development and continuing education support 

    A mission-driven team that values respect, inclusion, and innovation 

    Ready to Make an Impact? 

    Mission with Meaning: Be part of a purpose-led team committed to health equity and real-world impact. 

    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. 

    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. 

    Invested in Your Growth: We don’t just hire for today; we’re building the leaders and changemakers of tomorrow.  

    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

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  • Nurse Practitioner/Sub-Investigator  

    - Knoxville
    Job DescriptionJob DescriptionLocation: Knoxville, TNJob Type: Part-ti... Read More
    Job DescriptionJob Description

    Location: Knoxville, TN

    Job Type: Part-time, on-site

    Reports to: Medical Director 
     

    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 

    Conduct study visits including medical assessments, physical exams, and protocol-specific procedures. 

    Partner with principal investigators and research staff to ensure quality, safety, and regulatory compliance. 

    Engage participants with empathy—providing clear education, answering questions, and ensuring comfort throughout the trial process. 

    Identify, document, and report adverse events per protocol and regulatory standards. 

    Maintain accurate, timely, and high-quality documentation in source records and EDC systems. 

    Contribute to continuous improvement of workflows and study execution with a team-first mindset. 

    Occasional travel may be required for audits, site visits, or team meetings.  

    What You Bring 

    Active, unrestricted Nurse Practitioner license in Tennessee. 

    2+ years of clinical research experience (Phase 2–4 trials preferred). 

    Experience with GLP-1 therapies or metabolic/endocrine research highly preferred. 

    Strong knowledge of GCP/ICH guidelines; certification is a plus. 

    Excellent clinical judgment, attention to detail, and communication skills. 

    A collaborative spirit and commitment to doing what’s best for the patient and the team. 

    What We Offer 

    Competitive compensation 

    Medical, dental, and vision insurance 

    Generous PTO and paid holidays 

    Flexible scheduling options 

    Professional development and continuing education support 

    A mission-driven team that values respect, inclusion, and innovation 

    Ready to Make an Impact? 

    Mission with Meaning: Be part of a purpose-led team committed to health equity and real-world impact. 

    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. 

    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. 

    Invested in Your Growth: We don’t just hire for today; we’re building the leaders and changemakers of tomorrow.  

    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

    FBg3SGj9NR

    Read Less
  • Nurse Practitioner/Sub-Investigator  

    - Cary
    Job DescriptionJob DescriptionJob Type: Part-time, on-siteReports to:... Read More
    Job DescriptionJob Description

    Job Type: Part-time, on-site

    Reports to: Medical Director 
     

    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 

    Conduct study visits including medical assessments, physical exams, and protocol-specific procedures. 

    Partner with principal investigators and research staff to ensure quality, safety, and regulatory compliance. 

    Engage participants with empathy—providing clear education, answering questions, and ensuring comfort throughout the trial process. 

    Identify, document, and report adverse events per protocol and regulatory standards. 

    Maintain accurate, timely, and high-quality documentation in source records and EDC systems. 

    Contribute to continuous improvement of workflows and study execution with a team-first mindset. 

    Occasional travel may be required for audits, site visits, or team meetings.  

    What You Bring 

    Active, unrestricted Nurse Practitioner license in North Carolina. 

    2+ years of clinical research experience (Phase 2–4 trials preferred). 

    Experience with GLP-1 therapies or metabolic/endocrine research highly preferred. 

    Strong knowledge of GCP/ICH guidelines; certification is a plus. 

    Excellent clinical judgment, attention to detail, and communication skills. 

    A collaborative spirit and commitment to doing what’s best for the patient and the team. 

    What We Offer 

    Competitive compensation 

    Medical, dental, and vision insurance 

    Generous PTO and paid holidays 

    Flexible scheduling options 

    Professional development and continuing education support 

    A mission-driven team that values respect, inclusion, and innovation 

    Ready to Make an Impact? 

    Mission with Meaning: Be part of a purpose-led team committed to health equity and real-world impact. 

    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. 

    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. 

    Invested in Your Growth: We don’t just hire for today; we’re building the leaders and changemakers of tomorrow.  

    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

    APR5cFaKIy

    Read Less
  • Nurse Practitioner/Sub-Investigator  

    - West Jordan
    Job DescriptionJob DescriptionLocation: West Jordan, UtahJob Type: Par... Read More
    Job DescriptionJob Description

    Location: West Jordan, Utah

    Job Type: Part-time, on-site

    Reports to: Medical Director 
     

    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 

    Conduct study visits including medical assessments, physical exams, and protocol-specific procedures. 

    Partner with principal investigators and research staff to ensure quality, safety, and regulatory compliance. 

    Engage participants with empathy—providing clear education, answering questions, and ensuring comfort throughout the trial process. 

    Identify, document, and report adverse events per protocol and regulatory standards. 

    Maintain accurate, timely, and high-quality documentation in source records and EDC systems. 

    Contribute to continuous improvement of workflows and study execution with a team-first mindset. 

    Occasional travel may be required for audits, site visits, or team meetings.  

    What You Bring 

    Active, unrestricted Nurse Practitioner license in Utah. 

    2+ years of clinical research experience (Phase 2–4 trials preferred). 

    Experience with GLP-1 therapies or metabolic/endocrine research highly preferred. 

    Strong knowledge of GCP/ICH guidelines; certification is a plus. 

    Excellent clinical judgment, attention to detail, and communication skills. 

    A collaborative spirit and commitment to doing what’s best for the patient and the team. 

    What We Offer 

    Competitive compensation 

    Medical, dental, and vision insurance 

    Generous PTO and paid holidays 

    Flexible scheduling options 

    Professional development and continuing education support 

    A mission-driven team that values respect, inclusion, and innovation 

    Ready to Make an Impact? 

    Mission with Meaning: Be part of a purpose-led team committed to health equity and real-world impact. 

    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. 

    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. 

    Invested in Your Growth: We don’t just hire for today; we’re building the leaders and changemakers of tomorrow.  

    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

    bBobjw7laE

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  • Nurse Practitioner/Sub-Investigator  

    - Austin
    Job DescriptionJob DescriptionLocation: Austin, TXJob Type: Part-time,... Read More
    Job DescriptionJob Description

    Location: Austin, TX

    Job Type: Part-time, on-site

    Reports to: Medical Director 
     

    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 

    Conduct study visits including medical assessments, physical exams, and protocol-specific procedures. 

    Partner with principal investigators and research staff to ensure quality, safety, and regulatory compliance. 

    Engage participants with empathy—providing clear education, answering questions, and ensuring comfort throughout the trial process. 

    Identify, document, and report adverse events per protocol and regulatory standards. 

    Maintain accurate, timely, and high-quality documentation in source records and EDC systems. 

    Contribute to continuous improvement of workflows and study execution with a team-first mindset. 

    Occasional travel may be required for audits, site visits, or team meetings.  

    What You Bring 

    Active, unrestricted Nurse Practitioner license in Texas. 

    2+ years of clinical research experience (Phase 2–4 trials preferred). 

    Experience with GLP-1 therapies or metabolic/endocrine research highly preferred. 

    Strong knowledge of GCP/ICH guidelines; certification is a plus. 

    Excellent clinical judgment, attention to detail, and communication skills. 

    A collaborative spirit and commitment to doing what’s best for the patient and the team. 

    What We Offer 

    Competitive compensation 

    Medical, dental, and vision insurance 

    Generous PTO and paid holidays 

    Flexible scheduling options 

    Professional development and continuing education support 

    A mission-driven team that values respect, inclusion, and innovation 

    Ready to Make an Impact? 

    Mission with Meaning: Be part of a purpose-led team committed to health equity and real-world impact. 

    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. 

    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. 

    Invested in Your Growth: We don’t just hire for today; we’re building the leaders and changemakers of tomorrow.  

    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

    8lr3BswG8G

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  • Nurse Practitioner/Sub-Investigator  

    - Greenville
    Job DescriptionJob DescriptionJob Type: Part-time, on-siteReports to:... Read More
    Job DescriptionJob Description

    Job Type: Part-time, on-site

    Reports to: Medical Director 
     

    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 

    Conduct study visits including medical assessments, physical exams, and protocol-specific procedures. 

    Partner with principal investigators and research staff to ensure quality, safety, and regulatory compliance. 

    Engage participants with empathy—providing clear education, answering questions, and ensuring comfort throughout the trial process. 

    Identify, document, and report adverse events per protocol and regulatory standards. 

    Maintain accurate, timely, and high-quality documentation in source records and EDC systems. 

    Contribute to continuous improvement of workflows and study execution with a team-first mindset. 

    Occasional travel may be required for audits, site visits, or team meetings.  

    What You Bring 

    Active, unrestricted Nurse Practitioner license in South Carolina. 

    2+ years of clinical research experience (Phase 2–4 trials preferred). 

    Experience with GLP-1 therapies or metabolic/endocrine research highly preferred. 

    Strong knowledge of GCP/ICH guidelines; certification is a plus. 

    Excellent clinical judgment, attention to detail, and communication skills. 

    A collaborative spirit and commitment to doing what’s best for the patient and the team. 

    What We Offer 

    Competitive compensation 

    Medical, dental, and vision insurance 

    Generous PTO and paid holidays 

    Flexible scheduling options 

    Professional development and continuing education support 

    A mission-driven team that values respect, inclusion, and innovation 

    Ready to Make an Impact? 

    Mission with Meaning: Be part of a purpose-led team committed to health equity and real-world impact. 

    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. 

    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. 

    Invested in Your Growth: We don’t just hire for today; we’re building the leaders and changemakers of tomorrow.  

    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

    gVoZlYoikm

    Read Less
  • Nurse Practitioner/Sub-Investigator  

    - Tampa
    Job DescriptionJob DescriptionJob Type: Part-time, on-siteReports to:... Read More
    Job DescriptionJob Description

    Job Type: Part-time, on-site

    Reports to: Medical Director 
     

    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 

    Conduct study visits including medical assessments, physical exams, and protocol-specific procedures. 

    Partner with principal investigators and research staff to ensure quality, safety, and regulatory compliance. 

    Engage participants with empathy—providing clear education, answering questions, and ensuring comfort throughout the trial process. 

    Identify, document, and report adverse events per protocol and regulatory standards. 

    Maintain accurate, timely, and high-quality documentation in source records and EDC systems. 

    Contribute to continuous improvement of workflows and study execution with a team-first mindset. 

    Occasional travel may be required for audits, site visits, or team meetings.  

    What You Bring 

    Active, unrestricted Nurse Practitioner license in Florida. 

    2+ years of clinical research experience (Phase 2–4 trials preferred). 

    Experience with GLP-1 therapies or metabolic/endocrine research highly preferred. 

    Strong knowledge of GCP/ICH guidelines; certification is a plus. 

    Excellent clinical judgment, attention to detail, and communication skills. 

    A collaborative spirit and commitment to doing what’s best for the patient and the team. 

    What We Offer 

    Competitive compensation 

    Medical, dental, and vision insurance 

    Generous PTO and paid holidays 

    Flexible scheduling options 

    Professional development and continuing education support 

    A mission-driven team that values respect, inclusion, and innovation 

    Ready to Make an Impact? 

    Mission with Meaning: Be part of a purpose-led team committed to health equity and real-world impact. 

    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. 

    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. 

    Invested in Your Growth: We don’t just hire for today; we’re building the leaders and changemakers of tomorrow.  

    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

    m7YfqljeII

    Read Less
  • Nurse Practitioner/Sub-Investigator  

    - Independence
    Job DescriptionJob DescriptionJob Type: Part-time, on-siteReports to:... Read More
    Job DescriptionJob Description

    Job Type: Part-time, on-site

    Reports to: Medical Director 
     

    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 

    Conduct study visits including medical assessments, physical exams, and protocol-specific procedures. 

    Partner with principal investigators and research staff to ensure quality, safety, and regulatory compliance. 

    Engage participants with empathy—providing clear education, answering questions, and ensuring comfort throughout the trial process. 

    Identify, document, and report adverse events per protocol and regulatory standards. 

    Maintain accurate, timely, and high-quality documentation in source records and EDC systems. 

    Contribute to continuous improvement of workflows and study execution with a team-first mindset. 

    Occasional travel may be required for audits, site visits, or team meetings.  

    What You Bring 

    Active, unrestricted Nurse Practitioner license in Missouri. 

    2+ years of clinical research experience (Phase 2–4 trials preferred). 

    Experience with GLP-1 therapies or metabolic/endocrine research highly preferred. 

    Strong knowledge of GCP/ICH guidelines; certification is a plus. 

    Excellent clinical judgment, attention to detail, and communication skills. 

    A collaborative spirit and commitment to doing what’s best for the patient and the team. 

    What We Offer 

    Competitive compensation 

    Medical, dental, and vision insurance 

    Generous PTO and paid holidays 

    Flexible scheduling options 

    Professional development and continuing education support 

    A mission-driven team that values respect, inclusion, and innovation 

    Ready to Make an Impact? 

    Mission with Meaning: Be part of a purpose-led team committed to health equity and real-world impact. 

    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. 

    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. 

    Invested in Your Growth: We don’t just hire for today; we’re building the leaders and changemakers of tomorrow.  

    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! 

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  • Nurse Practitioner/Sub-Investigator  

    - Memphis
    Job DescriptionJob DescriptionJob Type: Part-time, on-siteReports to:... Read More
    Job DescriptionJob Description

    Job Type: Part-time, on-site

    Reports to: Medical Director 
     

    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 

    Conduct study visits including medical assessments, physical exams, and protocol-specific procedures. 

    Partner with principal investigators and research staff to ensure quality, safety, and regulatory compliance. 

    Engage participants with empathy—providing clear education, answering questions, and ensuring comfort throughout the trial process. 

    Identify, document, and report adverse events per protocol and regulatory standards. 

    Maintain accurate, timely, and high-quality documentation in source records and EDC systems. 

    Contribute to continuous improvement of workflows and study execution with a team-first mindset. 

    Occasional travel may be required for audits, site visits, or team meetings.  

    What You Bring 

    Active, unrestricted Nurse Practitioner license in Tennessee. 

    2+ years of clinical research experience (Phase 2–4 trials preferred). 

    Experience with GLP-1 therapies or metabolic/endocrine research highly preferred. 

    Strong knowledge of GCP/ICH guidelines; certification is a plus. 

    Excellent clinical judgment, attention to detail, and communication skills. 

    A collaborative spirit and commitment to doing what’s best for the patient and the team. 

    What We Offer 

    Competitive compensation 

    Medical, dental, and vision insurance 

    Generous PTO and paid holidays 

    Flexible scheduling options 

    Professional development and continuing education support 

    A mission-driven team that values respect, inclusion, and innovation 

    Ready to Make an Impact? 

    Mission with Meaning: Be part of a purpose-led team committed to health equity and real-world impact. 

    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. 

    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. 

    Invested in Your Growth: We don’t just hire for today; we’re building the leaders and changemakers of tomorrow.  

    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

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  • Nurse Practitioner/Sub-Investigator  

    - Goodlettsville
    Job DescriptionJob DescriptionJob Type: Part-time, on-siteReports to:... Read More
    Job DescriptionJob Description

    Job Type: Part-time, on-site

    Reports to: Medical Director 
     

    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 

    Conduct study visits including medical assessments, physical exams, and protocol-specific procedures. 

    Partner with principal investigators and research staff to ensure quality, safety, and regulatory compliance. 

    Engage participants with empathy—providing clear education, answering questions, and ensuring comfort throughout the trial process. 

    Identify, document, and report adverse events per protocol and regulatory standards. 

    Maintain accurate, timely, and high-quality documentation in source records and EDC systems. 

    Contribute to continuous improvement of workflows and study execution with a team-first mindset. 

    Occasional travel may be required for audits, site visits, or team meetings.  

    What You Bring 

    Active, unrestricted Nurse Practitioner license in Tennessee. 

    2+ years of clinical research experience (Phase 2–4 trials preferred). 

    Experience with GLP-1 therapies or metabolic/endocrine research highly preferred. 

    Strong knowledge of GCP/ICH guidelines; certification is a plus. 

    Excellent clinical judgment, attention to detail, and communication skills. 

    A collaborative spirit and commitment to doing what’s best for the patient and the team. 

    What We Offer 

    Competitive compensation 

    Medical, dental, and vision insurance 

    Generous PTO and paid holidays 

    Flexible scheduling options 

    Professional development and continuing education support 

    A mission-driven team that values respect, inclusion, and innovation 

    Ready to Make an Impact? 

    Mission with Meaning: Be part of a purpose-led team committed to health equity and real-world impact. 

    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. 

    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. 

    Invested in Your Growth: We don’t just hire for today; we’re building the leaders and changemakers of tomorrow.  

    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

    8RzdqzW8R0

    Read Less

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Astrid-Lindgren-Weg 12 38229 Salzgitter Germany