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Trial Science Jobs in Tennessee (NOW HIRING)

$110 - $160/hr

The (Senior) Scientific Project Manager will be responsible for providing project management ... Provide input into clinical trial documents (e.g., eCRFs, ICFs, SOWs). * Drive the delivery of data ...

New

Knowledge of scientific, medical, and regulatory terms * Must have an understanding of clinical research process * Knowledge of GCP and GMP * Computer skills with ability to use clinical trial ...

Knowledge of scientific, medical, and regulatory terms * Must have an understanding of clinical research process * Knowledge of GCP and GMP * Computer skills with ability to use clinical trial ...

Knowledge of scientific, medical, and regulatory terms * Must have an understanding of clinical research process * Knowledge of GCP and GMP * Computer skills with ability to use clinical trial ...

Knowledge of scientific, medical, and regulatory terms * Must have an understanding of clinical research process * Knowledge of GCP and GMP * Computer skills with ability to use clinical trial ...

Knowledge of scientific, medical, and regulatory terms * Must have an understanding of clinical research process * Knowledge of GCP and GMP * Computer skills with ability to use clinical trial ...

Knowledge of scientific, medical, and regulatory terms * Must have an understanding of clinical research process * Knowledge of GCP and GMP * Computer skills with ability to use clinical trial ...

Knowledge of scientific, medical, and regulatory terms * Must have an understanding of clinical research process * Knowledge of GCP and GMP * Computer skills with ability to use clinical trial ...

Knowledge of scientific, medical, and regulatory terms * Must have an understanding of clinical research process * Knowledge of GCP and GMP * Computer skills with ability to use clinical trial ...

Knowledge of scientific, medical, and regulatory terms * Must have an understanding of clinical research process * Knowledge of GCP and GMP * Computer skills with ability to use clinical trial ...

Knowledge of scientific, medical, and regulatory terms * Must have an understanding of clinical research process * Knowledge of GCP and GMP * Computer skills with ability to use clinical trial ...

Bachelor's degree in a relevant scientific discipline or healthcare-related field * Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and ...

Showing results 21-40

Trial Science information

See Tennessee salary details

$10

$34

$62

How much do trial science jobs pay per hour?

As of Aug 23, 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:

Infographic showing various Trial Science job openings in Tennessee as of August 2026, with employment types broken down into 1% As Needed, 80% Full Time, 17% Part Time, and 2% 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.

Senior Scientific Project Manager

LabConnect

On-site

$110 - $160/hr

Other

Medical, Life, Retirement, PTO

Posted 3 days ago

New


Job description

Remote - US, 2304 Silverdale Drive, Johnson City, Tennessee, United States of America

Job Description

Posted Friday, July 17, 2026 at 7:00 AM

Overview
LabConnect improves lives by partnering with pharmaceutical and biotech companies, and clinical research organizations (CROs) to accelerate the development of new medicines around the world.
We are an independent, global, one-stop-shop focused on delivering Central Laboratory Services that are tailor-made, timely and flexible to meet the evolving study demands of traditional to increasingly complex trials. Additionally, we provide Functional Service Provider (FSP) Solutions, supporting our clients with scientific and technical expertise, acting as an extension of their team, coordinating all laboratory related needs, advising on strategies for lab data collection and providing end-to-end analytical and logistical solutions.

The (Senior) Scientific Project Manager will be responsible for providing project management oversight to abiopharmaceutical client tasked with managing and executing analytical testing, methoddevelopment and/or validation of such assays as immunoassays, bioassays, pharmacokinetic and/or flow cytometry assays under Good Laboratory Practices (GLP). He/she will provide project management and technical support to teams conducting training, technical transfer, data review and trending analysis. The Sr. Project Manager must have the ability to effectively monitor the performance of CROs and service providers. The incumbent will also be responsible for operational documentation including SOPs, validation protocols and reports, transfer protocols and reports, and management reports.
What will you do?

  • Lead the contracting with third-party lab service providers for assay development and validation.
  • Collaborate with business operations, procurement, and clinical teams to ensure appropriate SOWs and contracts.
  • Study Coordination:
    • Manage critical reagent supply and sample analysis.
    • Work closely with bioanalytical strategy leads, clinical trial teams, and lab service providers to finalize study documents and meet timelines.
    • Support the development of novel Bioanalytical processes.
  • Documentation and Data:
    • Provide input into clinical trial documents (e.g., eCRFs, ICFs, SOWs).
    • Drive the delivery of data transfer specifications and ensure data accuracy.
  • Sample Logistics:
    • Track and reconcile sample testing, resolving any issues that arise.
    • Contribute to cleaning and finalizing data.

What will you bring to the table?

  • Bachelor’s, or Master’s level equivalent degree in Life Sciences or related field, required
  • 2 - 3 years' experience in the drug development and/or clinical trial processes for Scientific Project Manager, required
  • 5 - 6 years’ experience in the drug development and/or clinical trial processes for Senior Scientific Project Manager, required
  • Equivalent amount of experience managing projects, including timelines, budgeting and forecasting
  • Experience with method development, validation and troubleshooting
  • Extensive knowledge and experience in bioanalysis within regulatory environments (GLP/ GCP) to include experience with PK/ADA and/or biomarker analysis
  • Experience working in Oncology is preferred
  • PMP certified and formal change management training strongly preferred
  • Highly proficient in MS Office Suite, including MS Project, Word, Excel and PowerPoint, Smartsheet and SharePoint
  • Strong planning, attention to detail, communication, and organizational skills
  • Excellent verbal and written communication skills

Working Hours, Location, Travel:

US-based, EST preferred (alignment with working hours)

Fully remote position with potential for <5% travel

Join our team and discover how your work can impact patients' lives around the world!

Some of the Perks our LabConnectors Love:

  • Financial Security (Base Pay, 401k Match and Possible Annual Bonus Eligibility)
  • Health Benefits beginning on date of hire
  • PTO plan, plus 11 Paid Company Holidays, and 1 Day to Volunteer in your community
  • Short and Long-Term Disability, Life Insurance, and AD&D
  • We celebrate our differences, which enriches our culture!

In addition to great perks and challenging work assignments, we invest in our people with career growth opportunities, globally. We believe in a friendly and collaborative environment with open lines of communication. While living out our values ofPeople First, Quality Focused, Customer Centered, Technology Driven,andAccountability Always.

We are proud to be an Equal Employment Opportunity Employer and value the diversity of our workforce. We do not discriminate on the basis of race, gender, age, disability, religion, sexual orientation, or any other protected characteristic. To learn more about equal employment opportunity, please viewthe posters here:https://www.dol.gov/agencies/whd/posters

LabConnect also prioritizes the privacy and security of your personal data. All candidate information is handled in accordance with General Data Protection Regulation (GDPR). To learn more, please review our Privacy Notice on our website, by navigating to https://www.labconnect.com/

If you need assistance to complete your job application, search for a job opening, or submit an online application at LabConnect, please email talent@labconnect.com or call +1 (423) 722-3155.

Remote - US, 2304 Silverdale Drive, Johnson City, Tennessee, United States of America

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