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Full Time Clinical Research Rater Jobs in Tennessee

Research Assistant

Nashville, TN ยท On-site

$18.50 - $25.50/hr

This individual will support an NIH Phase 1 clinical trial investigating a naturalistic ... The Research Assistant II is a 30 hour, 75% full-time term position responsible for assisting with ...

Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing. Our client is a ... PERMANENT FULL TIME POSITION Overview: Under very limited supervision, responsible for selection ...

Research Assistant

Harrogate, TN ยท On-site

$15.75 - $21.50/hr

Position Details Position Information Position Title Research Assistant Department CVM Research Position Category Staff Full Time The Research Assistant shall provide ongoing clinical and research ...

Showing results 41-60

Full Time Clinical Research Rater information

What is a full time clinical research rater?

Full Time Clinical Research Raters are professionals who assess and document the progress, symptoms, and responses of patients participating in clinical research studies. They use standardized rating scales, interviews, and questionnaires to collect accurate data that helps determine the effectiveness and safety of new treatments or interventions. These raters play a vital role in ensuring the integrity and quality of clinical trial data, often working closely with clinicians, researchers, and study coordinators. Their responsibilities also include adhering to study protocols, maintaining patient confidentiality, and ensuring compliance with regulatory standards.

What are the key skills and qualifications needed to thrive as a full time clinical research rater?

Success as a Full Time Clinical Research Rater requires a background in psychology, neuroscience, or a related field, along with experience in clinical assessments and data collection. Familiarity with standardized rating scales, clinical trial databases, and regulatory compliance systems like Good Clinical Practice (GCP) certification is typically expected. Strong attention to detail, interpersonal communication, and objective judgment are crucial soft skills for accurate participant evaluation and collaboration with research teams. These competencies ensure reliable data collection, regulatory adherence, and the integrity of clinical research outcomes.

What are some typical challenges a full time clinical research rater may encounter, and how can they be managed?

Full Time Clinical Research Raters often face challenges such as managing large volumes of patient assessments, maintaining objectivity during subjective ratings, and adhering to strict study protocols. Balancing accuracy with efficiency is key, especially when dealing with sensitive patient information and tight study timelines. Collaborating closely with investigators and other research staff, participating in regular trainings, and using standardized rating tools can help ensure consistency and reliability in data collection.

What is the difference between Full Time Clinical Research Rater vs Part Time Clinical Research Rater?

AspectFull Time Clinical Research RaterPart Time Clinical Research Rater
Work HoursTypically 35-40 hours per weekLess than 20 hours per week
CertificationsOften requires relevant healthcare or research certificationsMay require similar certifications but less emphasis
Work EnvironmentFull-time employment in research facilities or remotePart-time roles, flexible locations
Employer UsageMajor research organizations, pharmaceutical companiesFreelance or contract research organizations

The main difference between a Full Time Clinical Research Rater and a Part Time Clinical Research Rater lies in work hours, certification emphasis, and employment type. Full-time roles offer consistent hours and benefits, while part-time positions provide flexibility. Both roles involve evaluating clinical data, but full-time positions are more integrated into research teams.

What are the most commonly searched types of Clinical Research Rater jobs in Tennessee?

The most popular types of Clinical Research Rater jobs in Tennessee are:

What are popular job titles related to Full Time Clinical Research Rater jobs in Tennessee?

For Full Time Clinical Research Rater jobs in Tennessee, the most frequently searched job titles are:

What cities in Tennessee are hiring for Full Time Clinical Research Rater jobs?

Cities in Tennessee with the most Full Time Clinical Research Rater job openings:

Nurse Practitioner/Sub-Investigator

Civia Health

Nashville, TN โ€ข On-site

Full-time

Medical, Dental, Vision, PTO

Re-posted 3 days ago


Job description

Job Type: Full-time, on-site
Reports to: Senior Manager, 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
  • 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.
  • 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 visionaryprofessionals 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!