clinical neuropsychologist

<div></div><div><div>Location Fayetteville, North Carolina Category Engineering, Technology, &amp; Science Job Type Full time Job Id R2125101 Posted Date 06/15/2026<br>
</div><p></p><div><div><div><div><div><div><div>
</div></div></div></div></div></div></div><div></div><div>JOB DESCRIPTION
</div><div><p><b>Title:</b></p>
Special Operations Psychometrist ( SWCS, Fort Bragg, NC)
<p></p><div><p><b>THIS POSITION OFFERS RELOCATION.</b></p></div><br>
<p></p><div><p>We attract the best minds in the world because our expertise thrives on creativity, resourcefulness and collaboration. That is how we supply our clients with cutting-edge solutions and services.</p></div><br>
<p></p><div><p>We are seeking a stellar <b>P</b><b>sychometrist</b><b> </b>who will perform assigned assessment procedures under the direct supervision of a credentialed privileged psychologist, operational psychologist, or neuropsychologist. At <b>KBR</b> we maintain a highly qualified workforce to help care for service people and astronauts &ndash; <i>Could this be you?</i></p></div><br>
<p></p><div><p><b>Essential Duties &amp; Responsibilities:</b></p>
</div><div><div><ul><li><p>Utilize therapeutic assessment and interview skills to elicit accurate and concise account of the patient&rsquo;s condition.</p>
</li><li><p>Screen patients to determine presenting problems and priority of appointment.</p>
</li><li><p>Perform basic assessment procedures, including initial screening evaluation and standardized neuropsychological, intelligence, and personality testing.</p>
</li><li><p>Conduct Assessment and Selection in large group settings as well as on an individual basis.</p>
</li><li><p>Assist credentialed providers with identifying mental health diagnosis and treatment strategies, as well as providing patient education.</p>
</li></ul></div></div><div><div><ul><li><p>Understand suitability requirements for the different units across the SOCOM enterprise.</p>
</li><li><p>Assist in providing specialized treatment and rehabilitation of brain injured and mental health patients.</p>
</li><li><p>Observe, monitor, report, and record patient interaction during assessment sessions.</p>
</li><li><p>Institute precautionary measures to prevent patient injuries due to suicide, homicide, or elopement.</p>
</li><li><p>Coordinate with other military agencies and MTFs regarding specialized care, treatment, and administrative functions.</p>
</li></ul></div></div><div><div><ul><li><p>Contact military or community agencies to obtain collateral information.</p>
</li><li><p>Explain and interpret neuropsychological services and procedures to access care to patients and commands.</p>
</li><li><p>Assist in or arrange for patient referral to other facilities for alternate level of care.</p>
</li><li><p>Other duties as assigned.</p><br>
</li></ul></div></div><p></p><div><div><p><b>Required Education/Experience/Skills/Training:</b></p>
</div><div><ul><li><p>This position requires U.S. Citizenship.</p>
</li><li><p>This position requires a Secret Clearance or Top Secret Clearance, or the ability to obtain a clearance.</p>
</li><li><p>This position requires a bachelor&rsquo;s degree from a formal program in psychology, sociology, or in a behavioral science related field from an accredited college or university.</p>
</li><li><p>Must be certified by the Board of Certified Psychometrists (BCP); this may be waived if the candidate has one (1) full year of full-time experience under the supervision of an operational psychologist or shall obtain the certification within the first year of employment.</p>
</li></ul></div></div><div><div><ul><li><p><b>This position requires a minimum of one (1) year of full-time work experience during the preceding three (3) years in the performance of psychological and/or neuropsychological testing and test scoring.</b></p>
</li><li><p>Fluent oral and written communication skills in English.</p>
</li><li><p>Must have and maintain current certification in Basic Cardiac Life Support (BCLS) by the American Heart Association as required for credentialing at servicing medical treatment facilities; front and back documentation of such training is required upon hire for credentialing.</p><br>
</li></ul></div></div><p></p><div><div><p><b>Desired Education, Experience, Skills or Training:</b></p>
</div><div><ul><li><p>Previous military background/experience.</p><br>
</li></ul></div><p></p><div><p><b>Standard Company Requirements:</b></p>
</div><div><ul><li><p>Must comply with Safety, Health and Environmental plan, policies and procedures.</p>
</li></ul></div></div><div><div><ul><li><p>Must comply with the Quality Assurance plan, policies and procedures.</p>
</li><li><p>Must maintain regular and acceptable attendance.</p>
</li><li><p>Responsible for completing all required training.</p>
</li><li><p>Perform other assignments and duties, as required.</p><br>
</li></ul></div></div><p></p><p>Belong, Connect and Grow at KBR
<br>
<br>
At KBR, we are passionate about our people and our Zero Harm culture. These inform all that we do and are at the heart of our commitment to, and ongoing journey toward being a People First company. That commitment is central to our team of team&rsquo;s philosophy and fosters an environment where everyone can Belong, Connect and Grow. We Deliver &ndash; Together.</p>
<p></p><p>KBR is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, disability, sex, sexual orientation, gender identity or expression, age, national origin, veteran status, genetic information, union status and/or beliefs, or any other characteristic protected by federal, state, or local law.</p></div></div><p></p>

Special Operations Psychometrist ( SWCS, Fort Bragg, NC)

Keiser University

<div><p>The Clinical Coordinator position plans, coordinates, facilitates, administers, and monitors, activities on behalf of the academic program and in coordination with academic and clinical faculty. These activities ensure the quality of our students learning experience during clinical education. Clinical Coordinators accomplish this through:</p><br>
<ul><li>
Assists with the development and assessment of the clinical education component of the curriculum with the Program Director.</li><li>
Coordination and implementation of the clinical education component of the curriculum including site placements, site visits, and evaluation.</li><li>
Responsible for facilitating students' clinical education.</li><li>
Responsible for ensuring clinical education program compliance.</li></ul><h1 class="jobSectionHeader"><b><br>
EDUCATION, EXPERIENCE AND TRAINING:</b></h1><ul><li>
Minimum of a bachelor's degree</li><li>
At least 2 years of clinical practice experience as an occupational therapist or occupational therapy assistant (ACOTE Standards).</li><li>
Current, unrestricted Florida licensed occupational therapist or occupational therapy assistant.</li></ul></div>

Clinical Coordinator- OTA (Academic Fieldwork Coordinator)

Sunrise Research Institute

<p><b>About 3Sync Research</b></p><p>3Sync Research is a growing clinical research organization dedicated to advancing medicine through high-quality clinical trials. We partner with leading pharmaceutical companies, CROs, physicians, and healthcare professionals to bring innovative treatment options to diverse patient populations.</p><p>Our office conducts outpatient clinical research across multiple therapeutic areas, including primary care, pediatrics, asthma/allergy, diabetes, endocrinology, infectious disease, vaccines, and other adult and pediatric studies. We are looking for a strong, experienced provider who is comfortable working directly with patients and supporting clinical trial oversight.</p><p><b>Position Overview</b></p><p>We are seeking a bilingual APRN / Nurse Practitioner to join our clinical research team as a Clinical Trial Sub-Investigator. This is an excellent opportunity for an experienced provider who is detail-oriented, and comfortable working with both adults and children.</p><p>In this role, you will work closely with the Principal Investigator, site directors, operations leadership, recruitment team, clinical research coordinators, sponsors, CROs, and regulatory teams to support the safe and compliant conduct of clinical trials. The Sub-Investigator will conduct patient screening, eligibility review, physical exams, safety assessments, protocol compliance, clinical documentation, enrollment support, participant retention, and contribute to overall site performance.</p><p><b>Key Responsibilities</b></p><p>Assist the Principal Investigator in the oversight and execution of clinical trials</p><p>Conduct patient screening, enrollment, and ongoing study visit assessments</p><p>Perform physical exams and clinical evaluations for adult and pediatric participants</p><p>Review medical history, medications, labs, vitals, inclusion/exclusion criteria, and study eligibility</p><p>Monitor participant safety throughout the study</p><p>Identify, assess, document, and report adverse events and clinical concerns</p><p>Perform or assist with blood draws, vital signs, and other protocol-required procedures</p><p>Review informed consent forms, source documents, lab reports, CRFs, and study records for accuracy and completeness</p><p>Support protocol compliance, data collection, and audit readiness</p><p>Communicate professionally with participants, parents/guardians, study staff, sponsors, CROs, and regulatory teams</p><p>Supervise and support clinical research staff when needed</p><p>Collaborate closely with site directors, operations leadership, recruitment teams, coordinators, and the Principal Investigator to support successful study outcomes, strong enrollment, participant retention, protocol compliance, and overall site performance</p><p>Serve as a team player within a fast-paced clinical research environment, helping ensure smooth communication between clinical, operational, and recruitment staff</p><p>Ensure study activities are conducted in compliance with FDA regulations, ICH-GCP guidelines, HIPAA, protocol requirements, and site SOPs</p><p><b>Requirements</b></p><p><b>Active and unrestricted</b> <b>License/Certification- Florida APRN / Nurse Practitioner License required</b></p><p>Minimum of 5+ years of experience as an APRN / Nurse Practitioner</p><p>(Bilingual English/Spanish )</p><p>Must be comfortable working with both adult and pediatric patients</p><p>Strong clinical assessment, documentation, and decision-making skills</p><p>Experience with patient evaluation, medical history review, medication review, labs, and clinical procedures</p><p>Phlebotomy or blood sampling experience preferred</p><p>Familiarity with medical terminology, clinical documentation, and outpatient patient care</p><p>Ability to work independently while collaborating with the Principal Investigator and research team</p><p>Strong attention to detail and ability to work in a fast-paced clinical environment</p><p>Professional, dependable, organized, proactive, and team-oriented</p><p>GCP certification preferred; training can be provided if needed</p><p>Availability to work occasional weekends as needed based on study requirements</p><p><b>Preferred Experience</b></p><p>Family Medicine</p><p>Primary Care</p><p>Pediatrics</p><p>Internal Medicine</p><p>Urgent Care</p><p>Allergy / Asthma</p><p>Endocrinology</p><p>Diabetes Care</p><p>Infectious Disease</p><p>Vaccines</p><p>Clinical Research</p><p>Clinical Trial Sub-Investigator experience</p><p><b>Ideal Candidate</b></p><p>The ideal candidate is an experienced, bilingual provider who is comfortable making clinical assessments, asking the right questions, identifying safety concerns, and working with a wide range of patients. We are looking for someone who is confident in their clinical judgment, reliable, personable, and able to take ownership of patient evaluations in a research setting.</p><p>This person should also be a strong team player who works well with site directors, operations leadership, recruitment teams, coordinators, and the Principal Investigator to help drive successful study outcomes, strong enrollment, participant retention, protocol compliance, and overall site performance.</p><p><b>Why Join 3Sync Research</b></p><p>Opportunity to work on innovative clinical trials and emerging treatments</p><p>Adult and pediatric patient population</p><p>Growing research organization with expanding study opportunities</p><p>Collaborative team environment</p><p>Exposure to multiple therapeutic areas</p><p>Flexible schedule available</p><p>Meaningful role in supporting patient safety and advancing clinical research</p><p><b>Benefits:</b></p><p>Health insurance</p><p>Dental insurance</p><p>Vision insurance</p><p>Paid time off</p><p>Pay: $88,117.74 - $106,120.29 per year</p><p>Benefits:</p><ul><li>Dental insurance</li><li>Health insurance</li><li>Paid time off</li><li>Vision insurance</li></ul><p>Work Location: In person</p>

Bilingual APRN / Nurse Practitioner

Huntsville Hospital Health System

<div>Overview:
<div>
Reporting to the manager, clinical informatics, the clinical informaticist is the hospital liaison for clinical informatics to the Medical Staff, Pharmacy and other Clinical Departments. Responsibilities will include: Physician systems orientation, CPOE execution, on-boarding, training and meaningful use compliance.
</div>Qualifications:
<div><b>
Education:</b> BSN required. Degree in clinical informatics or RNBC (Board Certified by the ANCC in nursing informatics) preferred.</div><div><b>
License:</b> Alabama Board of Nursing RN Degree &ndash; preferred. Current RNBC if no degree in clinical informatics, preferred.</div><div><b>
Experience:</b> Clinical work practice, Clinical Information Systems implementation, oversight or programming, Other positions requiring Medical Staff relationships and project development. Management experience.</div></div>

Clinical Informatics Specialist-Technical Services-FT-1st shift

Piper Companies

<div>
 <strong>
  Piper Companies
 </strong>
 is looking for an
 <strong>
  In-House Clinical Research Associate
 </strong>
 to join a clinical research company located in
 <strong>
  Bethesda, MD.
  <br/>
  <br/>
 </strong>
 <strong>
  Responsibilities of the In-House Clinical Research Associate include:
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Review and process essential regulatory documents received from clinical trial sites
  </li>
  <li>
   Request missing or additional documentation and respond to protocol or process-related inquiries
  </li>
  <li>
   Maintain and organize Trial Master Files (TMF) and centralized document systems
  </li>
  <li>
   Track regulatory documents and workflow in a centralized web-based system or database
  </li>
  <li>
   Ensure documents meet FDA, ICH GCP, and sponsor requirements for accuracy and completeness
  </li>
  <li>
   Troubleshoot regulatory document issues and follow up with study sites as needed
  </li>
  <li>
   Support distribution of trial-related materials and assist with study team coordination
  </li>
  <li>
   Assist with monitoring visit preparation and follow-up, including teleconference coordination
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Qualifications for the In-House Clinical Research Associate include:
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   3&ndash;5 years of experience in a clinical research setting
  </li>
  <li>
   Experience with regulatory document review/collection and knowledge of FDA and ICH GCP guidelines
  </li>
  <li>
   Experience with eTMF systems (e.g., Veeva Vault) and system administration skills
  </li>
  <li>
   Experience with Trial Master Files and centralized tracking systems
  </li>
  <li>
   Experience with IRB submissions and OHRP regulations is a plus
  </li>
  <li>
   Bachelor&rsquo;s degree required
  </li>
  <li>
   Strong organizational, communication, and time management skills
  </li>
  <li>
   Proficiency with Microsoft Office (Word, Excel, Outlook)
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Compensation for In-House Clinical Research Associate includes:
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Rate Range: $50,000&ndash;$80,000, depending on experience
  </li>
  <li>
   Comprehensive Benefit Package: Cigna Medical/Dental/Vision, 401K, Sick Leave as Required by Law
   <br/>
   <br/>
  </li>
 </ul>
 <em>
  This job is open for applications on June 1st, 2026. Applications will be accepted at least 30 days from the posting date.
  <br/>
  <br/>
 </em>
 Keywords: Clinical Research, Clinical Trials, Clinical Operations, In-House CRA, TMF, Trial Master File, eTMF, Veeva Vault, Regulatory Documents, Regulatory Affairs, Document Management, ICH GCP, FDA Regulations, Good Clinical Practice, Essential Documents, Site Document Collection, IRB Submissions, OHRP Regulations, Site Start-Up, Study Coordination, Clinical Study Support, Monitoring Support, TMF Maintenance, Document Tracking, Compliance, Audit Readiness, Clinical Data Management, Sponsor Oversight, CRO, Protocol Compliance, Investigator Communication, Site Management, Clinical Systems, Database Tracking, Microsoft Excel, Microsoft Word, Microsoft Outlook
 <br/>
 <br/>
</div>


In-House Clinical Research Associate

Combined Health Center Corp

<p><b>Job Overview</b><br/>We are seeking a dynamic and detail-oriented Research Coordinator/Medical Assistant to join our clinical research team. This role is vital in coordinating and supporting clinical trials, ensuring compliance with regulatory standards, and providing exceptional patient care. The ideal candidate will possess a strong foundation in medical terminology, clinical procedures, and research protocols, with a passion for advancing medical knowledge through meticulous data collection and management. This paid position offers an exciting opportunity to contribute to groundbreaking research projects while developing your skills in clinical development and regulatory compliance.</p><p><b>Duties</b></p><ul><li>Assist in the planning, organization, and execution of clinical trials, ensuring adherence to study protocols and regulatory guidelines such as FDA regulations and ICH GCP standards</li><li>Conduct patient monitoring by taking vital signs, performing blood sampling (phlebotomy), and documenting clinical observations accurately within electronic medical records (EMR) systems</li><li>Review and verify study documentation for accuracy, completeness, and compliance with protocol requirements</li><li>Manage data collection, entry, and management using statistical software and CDISC standards to ensure high-quality data integrity</li><li>Support clinical laboratory procedures, including specimen handling and processing, while maintaining strict compliance with HIPAA privacy regulations</li><li>Supervise or assist with research staff training on Good Clinical Practice (GCP) and study-specific procedures</li><li>Monitor patient safety throughout the trial process, including adverse event reporting and compliance management</li><li>Collaborate with investigators, sponsors, and regulatory bodies to ensure smooth trial operations and adherence to all applicable guidelines</li></ul><p><b>Experience</b></p><ul><li>Proven supervising experience in a clinical or research setting, demonstrating leadership in managing teams or projects</li><li>Hands-on experience managing clinical trials from initiation through closeout phases</li><li>Strong knowledge of medical terminology, clinical laboratory procedures, and blood sampling techniques (phlebotomy)</li><li>Familiarity with EMR systems, data management tools, statistical software, and CDISC standards for data collection and analysis</li><li>Understanding of FDA regulations, ICH GCP guidelines, HIPAA privacy rules, and clinical development processes</li><li>Certification in Good Clinical Practice (GCP) from a recognized issuer such as the ICH GCP certificate or equivalent is required; valid certification for California (CA) preferred</li><li>Experience working within clinical research environments involving blood sampling, vital signs assessment, and patient monitoring</li><li>Ability to review complex documentation meticulously while maintaining high standards of compliance and accuracy</li></ul><p>Join us in advancing innovative healthcare solutions! This role offers the chance to work at the forefront of clinical research while honing your skills in a collaborative environment dedicated to excellence. We value motivated professionals eager to make a difference through meticulous research practices combined with compassionate patient care.</p><p>Pay: $35,500.96 - $50,000.00 per year</p><p>Work Location: In person</p>

Research Coordinator/ Medical Assistant

Elevate Clinical Research

<div><p><b>About Company:</b></p><p>
Elevate Clinical Research is a mission‑driven organization expanding access to high‑quality clinical trials across <b>Texas, Louisiana, Illinois, Maryland, Kansas</b>, and growing. We exist to bring research closer to the communities that need it most, delivering compassionate patient care, operational excellence, and trustworthy data that advances medicine.</p><p>
At Elevate, your work has real impact. Every role contributes directly to improving health outcomes and bringing new therapies to life. We hire people who care deeply about patients, believe in doing things the right way, and want to grow with a company that&rsquo;s expanding nationwide.</p><p><b>
What We Value</b></p><ul><li><p>
Patients first in every decision and interaction</p></li><li><p>
Access, equity, and bringing research to underserved communities</p></li><li><p>
High‑quality, compliant, reliable study execution</p></li><li><p>
Purpose‑driven growth and opportunities for advancement</p></li><li><p>
Supportive teams who communicate, collaborate, and care</p></li></ul><p><b>
Why People Join Us</b></p><ul><li><p>
A mission that matters</p></li><li><p>
Clear, structured onboarding</p></li><li><p>
Leadership that listens and supports</p></li><li><p>
Career growth as we expand into new states</p></li><li><p>
A culture built on integrity, teamwork, and accountability</p></li></ul><p>
Join Elevate and help build a patient‑centered research network that&rsquo;s changing what clinical trials can look like for communities across the country.</p><p><b>
About the Role:</b></p><p>
The Clinical Research Coordinator (CRC) plays a pivotal role in the successful execution and management of clinical trials within healthcare settings. This position is responsible for coordinating all aspects of clinical research studies, ensuring compliance with regulatory requirements and institutional policies. The CRC serves as a liaison between investigators, study sponsors, and participants, facilitating effective communication and smooth study progression. By meticulously managing patient recruitment, data collection, and study documentation, the CRC ensures the integrity and quality of clinical research data. Ultimately, this role contributes to advancing medical knowledge and improving patient care through the rigorous conduct of clinical research.</p><p><b>
Minimum Qualifications:</b></p><ul><li>
Bachelor&rsquo;s degree in a health-related field such as Nursing, Life Sciences, or Public Health.</li><li>
At least 2 years of experience coordinating clinical research studies or trials.</li><li>
Comprehensive knowledge of clinical trial processes, regulatory requirements, and ethical standards.</li><li>
Familiarity with clinical research documentation, including informed consent forms and case report forms.</li><li>
Strong organizational skills and attention to detail to manage multiple study activities simultaneously.</li></ul><p><b>
Preferred Qualifications:</b></p><ul><li>
Certification as a Clinical Research Coordinator (e.g., ACRP-CRC or SOCRA).</li><li>
Experience working with electronic data capture (EDC) systems and clinical trial management systems (CTMS).</li><li>
Advanced knowledge of FDA regulations and Institutional Review Board (IRB) processes.</li><li>
Previous experience in patient recruitment and retention strategies for clinical studies.</li><li>
Master&rsquo;s degree in Clinical Research, Public Health, or a related discipline.</li></ul><p><b>
Responsibilities:</b></p><ul><li>
Coordinate and oversee the daily operations of clinical trials, including patient recruitment, informed consent, and scheduling study visits.</li><li>
Ensure compliance with all regulatory requirements, institutional policies, and Good Clinical Practice (GCP) guidelines throughout the study lifecycle.</li><li>
Maintain accurate and up-to-date regulatory documents, case report forms, and study databases to support data integrity and audit readiness.</li><li>
Monitor study progress and patient safety by conducting regular assessments and reporting adverse events to the appropriate parties.</li><li>
Collaborate with investigators, sponsors, and multidisciplinary teams to facilitate effective communication and resolve study-related issues promptly.</li></ul><p><b>
Skills:</b></p><p>
The required skills such as clinical trials coordination, regulatory document management, and patient recruitment are essential for ensuring that studies are conducted efficiently and ethically. Clinical monitoring and trial management skills enable the coordinator to oversee study progress and maintain compliance with protocols and regulations. Proficiency in clinical research and clinical practice allows the coordinator to understand medical terminology and patient care considerations, facilitating effective communication with healthcare providers and participants. Preferred skills like experience with electronic data systems and advanced regulatory knowledge enhance the ability to manage complex data and navigate regulatory landscapes. Together, these skills support the daily responsibilities of maintaining study integrity, safeguarding participant safety, and contributing to the advancement of healthcare research.</p></div>

Clinical Research Coordinator

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