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Trial Science Jobs in Florida (NOW HIRING)

Summit Therapeutics

Sr. Clinical Trial Associate

Miami, FL

$32 - $43.75/hr

SENIOR CLINICAL TRIAL ASSOCIATE Location: ONSITE - Miami, FL Overview of Role: The Senior Clinical ... Bachelor's degree in biological sciences, health sciences or medical field, or equivalent ...

Summit Therapeutics

Sr. Clinical Trial Associate

Miami, FL · On-site

$32 - $43.75/hr

SENIOR CLINICAL TRIAL ASSOCIATE Location: ONSITE - Miami, FL Overview of Role: The Senior Clinical ... Bachelor's degree in biological sciences, health sciences or medical field, or equivalent ...

IQVIA

Clinical Trial Psych Rater

Coral Gables, FL · Remote

$62K - $156K/yr

Our team combines deep scientific expertise with cutting-edge technology to deliver high-quality ... clinical trial data. This position involves reviewing scales administered by raters to confirm ...

Syneos Health, Inc.

Medical Science Liaison

Miami, FL · On-site

$190 - $210/hr

Knowledge of clinical trial/research design, conduct, and understanding of clinical study results * Deep scientific knowledge and genuine passion for Neurology & Rare Disease * Experience in Epilepsy ...

Syneos Health

Medical Science Liaison

Jacksonville, FL · On-site

$190 - $210/hr

Knowledge of clinical trial/research design, conduct, and understanding of clinical study results. * Deep scientific knowledge and genuine passion for Neurology & Rare Disease. * Experience in ...

Syneos Health, Inc.

Medical Science Liaison

Orlando, FL · On-site

$190 - $210/hr

Knowledge of clinical trial/research design, conduct, and understanding of clinical study results * Deep scientific knowledge and genuine passion for Neurology & Rare Disease * Experience in Epilepsy ...

Syneos Health

Medical Science Liaison

Orlando, FL · On-site

$190 - $210/hr

Knowledge of clinical trial/research design, conduct, and understanding of clinical study results * Deep scientific knowledge and genuine passion for Neurology & Rare Disease * Experience in Epilepsy ...

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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 Florida is $28.15, according to ZipRecruiter salary data. Most workers in this role earn between $19.23 and $35.91 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 Florida look for?

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

Trial Science jobs near you
Infographic showing various Trial Science job openings in Florida as of August 2026, with employment types broken down into 1% As Needed, 76% Full Time, 20% Part Time, and 3% Contract. Highlights an 73% Physical, 4% Hybrid, and 23% Remote job distribution, with an average salary of $58,548 per year, or $28.1 per hour.

Sr. Clinical Trial Associate

Summit Therapeutics

Miami, FL

$32 - $43.75/hr

Full-time

Posted 4 days ago

Job description

 SENIOR CLINICAL TRIAL ASSOCIATE

Location: ONSITE - Miami, FL

Overview of Role:

The Senior Clinical Trial Associate (Senior CTA) is an experienced clinical operations professional who is responsible for supporting the daily workflow of clinical operations activities. They will provide robust administrative support to study teams throughout the study. Key administrative activities include, but are not limited to, managing meeting invitations, creating agendas and meeting minutes, study document filing, maintaining study trackers, and oversight of the eTMF and vendors.

Role and Responsibilities:

  • Provides comprehensive administrative support to the clinical operations study team,including managing meeting logistics, creating agendas, and drafting meeting minutes, withminimal oversite
  • Executes tasks as assigned by the Clinical Operations Manager, including study budgetforecasting and tracking
  • Ensures accurate and timely documentation, including eTMF management, study contractsand financial records in compliance with ICH-GCP, company policies and regulatoryrequirements
  • Coordinates clinical operations activities across cross-functional teams, including contractmanagement, vendor oversight, site start-up and activation, protocol deviation
  • Creates and maintains study-related materials, such as country and site binders and trackstrial milestones
  • Ensure the eTMF is being maintained up-to-date and all essential documents areappropriately filed in the eTMF
  • Collaborates with CROs to ensure accurate data collection and entry into the CTMS andEDC
  • Attend and contribute to team meetings, taking detailed meeting minutes
  • Supports clinical study management as delegated by Clinical Operations managers, including liaison with external vendors
  • Actively participates in process improvement initiatives to enhance clinical operations efficiency
  • All other duties as assigned

Experience, Education and Specialized Knowledge and Skills:

  • Bachelor's degree in biological sciences, health sciences or medical field, or equivalent combination of education and experience required 4+ years of experience in clinical study environment within CRO or Pharmaceutical company
  • Experience using Clinical Trial Management Systems (CTMS) and Clinical Trial Master File Systems (eTMF) required Strong understanding of the phases of clinical drug development and clinical operation processes from start-up to close-out
  • Knowledge of applicable FDA Code of Federal Regulations, Good Clinical Practices, and ICH guidelines
  • Ability to organize, prioritize tasks, identify and resolve issues efficiently. Manage multiple tasks effectively and follow through on assigned tasks.
  • Ability to receive general instructions on new assignments and perform routine work independently. Collaborate and work effectively within a team and within a multi-disciplinary environment.
  • Outstanding interpersonal skills coupled with the ability to communicate effectively in both oral and written form
  • Attention to detail, accuracy and confidentiality

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