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$10

$34

$62

How much do trial science jobs pay per hour?

As of Aug 24, 2026, the average hourly pay for trial science in Tennessee is $34.19, according to ZipRecruiter salary data. Most workers in this role earn between $23.37 and $43.65 per hour, depending on experience, location, and employer.

What is trial science?

A Trial Science job involves applying psychology, research, and analytics to legal proceedings to help attorneys build effective trial strategies. Trial scientists study jury behavior, conduct mock trials, develop case themes, and advise on witness preparation. They use social science techniques to assess juror attitudes and improve courtroom persuasion. Their goal is to maximize the effectiveness of legal arguments and presentation to achieve favorable case outcomes.

What does a trial science professional do?

A professional in Trial Science typically collaborates closely with attorneys to conduct jury research, prepare witness testimony, and develop case presentations. The workflow often includes designing and analyzing mock trials, conducting focus groups, and interpreting juror feedback to inform trial strategy. There is a strong emphasis on teamwork and communication, as you'll regularly present findings to legal teams and adapt recommendations based on evolving case needs. This role offers exposure to a variety of cases and provides opportunities to develop expertise in both psychology and litigation support, making it rewarding for those who enjoy dynamic, research-driven environments.

What are the key skills and qualifications needed to thrive in trial science?

To excel in Trial Science, you need a solid background in psychology, data analysis, and research methodologies, often supported by an advanced degree in psychology, law, or social sciences. Familiarity with software for jury research, survey design, statistical analysis, and experience with mock trial technology is important. Outstanding communication, analytical thinking, and interpersonal skills help you interpret data and work seamlessly with legal teams. These competencies are essential for providing actionable insights that shape trial strategies and enhance litigation outcomes.

How to become a trial science?

To become a trial scientist, typically a background in life sciences, medicine, or related fields is required, along with strong analytical skills and knowledge of clinical trial protocols. Relevant education includes a bachelor's degree or higher, and experience with data management and regulatory standards such as GCP is beneficial. Certification or training in clinical research can also enhance job prospects.

What does a trial scientist do?

A trial scientist designs, manages, and analyzes clinical trials to evaluate the safety and effectiveness of new medical treatments or products. They often work with regulatory guidelines, collect and interpret data, and collaborate with healthcare professionals and research teams. Strong knowledge of scientific methods, data analysis, and regulatory compliance is essential in this role.

What job categories do people searching Trial Science jobs in Tennessee look for?

The top searched job categories for Trial Science jobs in Tennessee are:

Trial Science jobs near you
Infographic showing various Trial Science job openings in Tennessee as of August 2026, with employment types broken down into 1% As Needed, 75% Full Time, 21% Part Time, and 3% Contract. Highlights an 73% Physical, 4% Hybrid, and 23% Remote job distribution, with an average salary of $71,109 per year, or $34.2 per hour.

Clinical Trial Specialist

Midtown, TN

Tennessee Oncology
Health Care and Social Assistance • 501 - 1,000 employees

6.8

Company rating: 6.8 out of 10

Based on 27 frontline employees who took The Breakroom Quiz

People enjoy working here

Recommended by parents

Respectful managers

Learn more about Tennessee Oncologyexternal

Full-time

Posted 18 days ago

Job description

Tennessee Oncology, one of the nation's largest, community-based cancer care specialists, is home to one of the leading clinical trial networks in the country. Established 1976 in Nashville, Tennessee Oncology's mission remains unchanged: To provide access to high-quality cancer care and the expertise of clinical research for all patients, at convenient locations within their community and close to their home. Our growing network of physicians and locations is based on this mission. Tennessee Oncology is committed to advancing both the science of detection and targeted treatments, and to making these advances available to every patient. We believe caring for cancer patients is a privilege.

Why Join Us? We are looking for talented and highly-motivated individuals who demonstrate a natural desire to support the meaningful work of community oncologists and the patients we serve.

Job Description:

This position works closely with the research team to help coordinate the approval processes and conduct of research protocols, assured that the integrity and quality of the research is maintained and that the research is conducted in accordance with Good Clinical Practice Guidelines, federal and sponsor regulations and guidelines, GHCR policies and procedures, and research protocols. The Clinical Trial Specialist I will assist in the management of subjects on clinical trials and coordinating activities associated with clinical trials under the mentorship and guidance of a Clinical Trial Specialist II.

ESSENTIAL FUNCTIONS:

  • Manage and execute the day-to-day operations of complex Phase I-IV clinical research protocols in compliance with applicable GCP/ICH guidelines and other regulatory requirements
  • Manage and lead cross-functional study teams, including vendors; liaise with other functional areas (preclinical development, pharmaceutical sciences, safety, and regulatory affairs) in order to accurately coordinate clinical study activity.
  • Provides second check for patient eligibility to clinical trial, following review by research nurse, including a second check of inclusion/exclusion requirements and eligibility criteria
  • Attend and oversee Site Initiation Visits
  • Coordinate and attend regular monitoring visits and closeout visits
  • Maintains informed consents records of each patient for the duration of a study
  • Maintains and files all relevant study documents throughout lifetime of a trial
  • Provides regular and concise updates on study timelines, patient statuses, and trial details to study teams, Principal Investigator, and study sponsor.
  • Meets data management deadlines set by internal and external teams
  • Acts as a point of contact for Research Data Coordinator, and assists with and reviews data entry where necessary
  • Protects the rights, safety, and welfare of patients
  • Strives to maintain harmonious relationships with clinic personnel, clients, and administrative staff
  • Reviews newly activated protocols, amendments, notices, suspensions, and terminations
  • Maintains required certification in Good Clinical Practice and Good Documentation Practice
  • Serves as a liaison to multiple Tennessee Oncology departments, providers, and other personnel
  • Serves as a liaison between GHCR and external clients and sponsors
  • Maintains a professional approach respecting the dignity and confidentiality of patients
  • Maintains a good attendance record and reports to work on time
  • Maintains a professional attitude and appearance
  • Proactively identifies trial-related issues and provides recommendations for resolution
  • Executes job responsibilities with the understanding of how output would affect, and impact other areas related to own job area/team with occasional guidance

KNOWLEDGE, SKILLS & ABILITIES:

  • Ability to independently handle multiple priorities in a fast-paced environment
  • Ability to comprehend complex clinical trial protocols
  • Microsoft Office product knowledge (Word, Excel, PowerPoint, SharePoint and OneNote)

EDUCATION & EXPERIENCE:

  • Bachelor's Degree or equivalent combination of education and experience required
  • One year of experience working in clinical trials required

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