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Trial Science Jobs in Georgia (NOW HIRING)

IQVIA

Scientific Support Senior Scientist

Marietta, GA · On-site +1

$58K - $122K/yr

We are seeking a Scientific Support Senior Scientist to join IQVIA Laboratories at Marietta, GA. We ... Understanding of the clinical trial process and associated dependencies * Proficiency with ...

New

IQVIA

Scientific Support Senior Scientist

Marietta, GA · On-site +1

$58K - $122K/yr

We are seeking a Scientific Support Senior Scientist to join IQVIA Laboratories at Marietta, GA. We ... Understanding of the clinical trial process and associated dependencies * Proficiency with ...

New

IQVIA

Clinical Project Lead, Oncology

Atlanta, GA · Remote

$68K - $232K/yr

Bachelor's degree in life sciences, healthcare, or related field * Strong knowledge of ICH-GCP, regulatory requirements, and clinical trial processes * Excellent communication and stakeholder ...

IQVIA

Clinical Project Lead, Oncology

Atlanta, GA · Remote

$68K - $232K/yr

Bachelor's degree in life sciences, healthcare, or related field * Strong knowledge of ICH-GCP, regulatory requirements, and clinical trial processes * Excellent communication and stakeholder ...

Capstone Search Partners

IP Paralegal

Decatur, GA

$60K - $92K/yr

... sciences. The firm prides itself on delivering exceptional legal services and fostering a ... Prepare exhibits, binders, and other trial-related materials. * Ensure compliance with court rules ...

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How much do trial science jobs pay per hour?

As of Aug 23, 2026, the average hourly pay for trial science in Georgia is $31.81, according to ZipRecruiter salary data. Most workers in this role earn between $21.73 and $40.58 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 Georgia look for?

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

What cities in Georgia are hiring for Trial Science jobs?

Cities in Georgia with the most Trial Science job openings:

Trial Science jobs near you
Infographic showing various Trial Science job openings in Georgia as of August 2026, with employment types broken down into 1% As Needed, 70% Full Time, 19% Part Time, 7% Contract, and 3% Nights. Highlights an 73% Physical, 4% Hybrid, and 23% Remote job distribution, with an average salary of $66,155 per year, or $31.8 per hour.

Clinical Research Quality Control Associate

CenExel

Decatur, GA • On-site

Full-time

Medical, Dental, Vision, Life, Retirement

Re-posted 29 days ago

CenExel rating

7.5

Company rating: 7.5 out of 10

Based on 6 frontline employees who took The Breakroom Quiz

64th of 120 rated laboratories

Job description

About Us:
CenExel is a leading nationwide clinical research site and patient network serving the life sciences industry. Leading in CNS and early phase studies, our 18 science-led Centers of Excellence deliver the right patients, at the right time, in the right place. Recently acquired by BayPine Capital Partners, our research sites provide unparalleled medical and scientific support in the design and execution of clinical trials. Our world-class PIs, advanced patient engagement strategies, premium data analytics, and integrated operations optimize every step of the clinical trial process.
Along with an exceptional work environment that promotes teamwork, positive leadership, and optimal work-life balance, CenExel Clinical Research also provides highly competitive compensation and a generous benefits package to full time employees after 30 days of employment including Health Insurance, Dental, Vision, LTD, STD, Life Ins, and 401k.
Job Summary:
The Clinical Research Quality Control (QC) Associate is responsible for ensuring the accuracy, consistency, and integrity of clinical trial documentation and processes. Working closely with clinical operations, data management, and regulatory teams, the QC Associate reviews essential trial documents and clinical data to verify compliance with GCP (Good Clinical Practice), ICH guidelines, regulatory requirements, and internal SOPs.
Essential Responsibilities and Duties:
  • Performs quality control reviews of clinical trial documents (e.g., informed consent forms, case report forms, regulatory binders, monitoring visit reports) to ensure accuracy, completeness, and consistency.
  • Identifies discrepancies, deviations, or data entry errors and follow up with appropriate teams for resolution.
  • Supports the preparation and QC of Trial Master File (TMF) documents (paper and/or electronic).
  • Assists in internal audits and inspection readiness activities.
  • Collaborates with cross-functional teams (clinical operations, data management, regulatory affairs) to maintain high standards in documentation practices.
  • Maintains and tracks QC metrics and contribute to quality improvement initiatives.
  • Ensures that all clinical documentation complies with GCP, ICH, FDA, EMA, and company SOPs.
  • Assists with SOP development and updates related to quality control activities.
  • Supports and ensures strictest adherence to best practices, FDA Code of Federal Regulations, ICH (International Conference on Harmonization), GCP (Good Clinical Practices), CenExel standard operating procedures, site working Practices, protocol, and company guidelines and policies.
  • Assumes other duties and responsibilities as assigned. The above responsibilities are a general description of the level and nature of the work assigned to this classification and are not to be considered as all inclusive.

Education/Experience/Skills:
  • Must be able to effectively communicate verbally and in writing.
  • Bachelor's degree in life sciences, healthcare, or a related field required. Advanced degree preferred.
  • 1-3 years of experience in clinical research, with at least 1 year in a QC, QA, or documentation review role.
  • Familiarity with clinical trial processes and regulatory requirements (GCP, ICH, FDA, EMA).
  • Experience with electronic systems such as eTMF, EDC, and CTMS preferred.
  • Strong attention to detail and organizational skills.
  • Excellent written and verbal communication.
  • Ability to work independently and in a team-oriented environment.
  • Proficiency in Microsoft Office (Word, Excel, Outlook, PowerPoint).
  • Certification in clinical research (e.g., ACRP, SOCRA) is a plus.
  • Experience in Phase I-IV trials or in a CRO environment.

Working Conditions
  1. Indoor, Office environment.
  2. Indoor, Clinic environment.
  3. Essential physical requirements include sitting, typing, standing, and walking.
  4. Lightly active position, occasional lifting of up to 20 pounds.
  5. Reporting to work, as scheduled, is essential.
  6. Occasional travel may be required (e.g., for audits or training).

CenExel Clinical Research is an Equal Opportunity Employer. All applicants will be considered for employment without regards to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran, or status.
Equal Opportunity Employer
This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor.

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