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Full Time Clinical Research Rater Jobs in Tennessee

ECN Operating LLC

Clinical Research Coordinator

Smyrna, TN

$22.50 - $30/hr

We are seeking a highly organized and motivated Clinical Research Coordinator (CRC) to join our ... Job Type: Full-time Work Location: In person Schedule: * 8 hour shift * Monday to Friday * Weekends ...

Actalent

Oncology Clinical Research Nurse

Nashville, TN

$75K - $102K/yr

Eligibility: * Full-time employees are eligible to set up and contribute to the 401(K) plan once ... Accrual Rates: * Length of service determines the rate at which the team member will accrue PTO.

Alira Health

Clinical Research Associate

Milan, TN · On-site

... rates, and responds to sponsor requests. * Conducts audit preparation at study sites as needed ... clinical research experience TECHNICAL COMPETENCES & SOFT SKILLS * Ability to travel. * Proven ...

Covenant Health

Clin Research Nurse Coord

Knoxville, TN · On-site

$65K - $82K/yr

Registered Nurse Coordinator, Cardiology Clinical Research Full Time, 80 Hours Per Pay Period, Day Shift Covenant Health Cancer Centers Overview: Covenant Health Cancer Center is our region's largest ...

Covenant Health

Clin Research Nurse Coord

Knoxville, TN · On-site

$65K - $82K/yr

Overview Registered Nurse Coordinator, Cardiology Clinical Research Full Time, 80 Hours Per Pay Period, Day Shift Covenant Health Cancer Centers Overview: Covenant Health Cancer Center is our region ...

Covenant Health

Clin Research Nurse Coord

Knoxville, TN · On-site

$65K - $82K/yr

Overview Registered Nurse Coordinator, Oncology Clinical Research Full Time, 80 Hours Per Pay Period, Day Shift Thompson Cancer Survival Center Overview: Thompson Cancer Survival Center is our region ...

Covenant Health

Clin Research Nurse Coord

Knoxville, TN · On-site

$65K - $82K/yr

Registered Nurse Coordinator, Oncology Clinical Research Full Time, 80 Hours Per Pay Period, Day Shift Thompson Cancer Survival Center Overview: Thompson Cancer Survival Center is our region ...

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All JobsClinical Research Rater JobsFull Time Clinical Research Rater JobsFull Time Clinical Research Rater Jobs in Tennessee

Full Time Clinical Research Rater information

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 key skills and qualifications needed to thrive as a Full Time Clinical Research Rater, and why are they important?

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 Full Time Clinical Research Raters?

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 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:
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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:
Full Time Clinical Research Rater jobs near you

Clinical Research Coordinator

ECN Operating LLC

Smyrna, TN

$22.50 - $30/hr

Full-time

Posted 10 days ago

Job description

Job Summary:

We are seeking a highly organized and motivated Clinical Research Coordinator (CRC) to join our research team. The CRC will coordinate and support all aspects of clinical trials and research studies, including subject recruitment, data collection, regulatory compliance, and specimen handling. Candidates with current Phlebotomy certification or Medical Assistant (MA) certification are strongly preferred, as this role may include specimen collection and basic clinical procedures.

Key Responsibilities:

  • Coordinate day-to-day clinical research activities to ensure study protocols are followed.
  • Recruit, screen, and enroll study participants.
  • Obtain informed consent and ensure ethical conduct in all study interactions.
  • Collect, process, and ship biological specimens per protocol (e.g., blood draws, urine samples).
  • Perform basic clinical procedures as permitted by certification (e.g., vital signs, EKGs).
  • Maintain accurate and timely documentation in case report forms and electronic databases.
  • Communicate with sponsors, monitors, and IRBs regarding study progress and compliance.
  • Schedule participant visits and follow-ups; ensure visit windows are met.
  • Ensure proper storage, handling, and accountability of investigational products, if applicable.
  • Maintain regulatory documents and assist with IRB submissions.

Qualifications:

  • Bachelor's degree in a health-related field required.
  • At least 1–2 years of experience in clinical research preferred.
  • Phlebotomy certification or MA certification preferred.
  • Knowledge of Good Clinical Practice (GCP) and regulatory guidelines.
  • Excellent organizational skills and attention to detail.
  • Strong interpersonal and communication skills.
  • Proficiency in Microsoft Office and electronic data capture systems (e.g., REDCap, EDC platforms).
  • Ability to work independently and as part of a multidisciplinary team.

Preferred Qualifications:

  • Experience working in clinical trials, especially in a hospital or academic setting.
  • Familiarity with IRB processes and clinical trial documentation.
  • Bilingual skills (depending on patient population) may be a plus.

Job Type: Full-time

Work Location: In person

Schedule:

  • 8 hour shift
  • Monday to Friday
  • Weekends as needed

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