1

Trial Science Jobs (NOW HIRING)

Preference for undergraduate degree in Biological Sciences or professions (pharmacy, medicine ... Trial Interactive CTMS, Medidata CTMS) preferred. * Demonstrated track record of successfully ...

Clinical Trial Manager

$130K - $150K/yr

Our cutting-edge science and robust clinical pipeline form the broadest PRAME franchise with the ... Role Overview: We are seeking a Clinical Trial Manager (CTM) to support our U.S. Clinical ...

... trial science lead, or similar client-facing scientific role. * Minimum four years of hands-on experience with administration and/or training of clinical rating scales and study endpoints.

The ideal Clinical Trial Laboratory Manager holds a Bachelor's degree in a science-related field and possesses experience with blood collection and/or laboratory processing. Prior experience with ...

POSITION SUMMARY This Clinical Trial Manager role is responsible for leading the end-to-end ... BA/BS in Science, Life Sciences or relevant field; or equivalent combination of education and ...

Clinical Trial Manager

San Francisco, CA · On-site

$145K - $165K/yr

Degree in Life Sciences & industry-sponsored clinical trial experience: * BS & 3+ years * MS/MPH & 1+ years * Experience with or managing CROs; either from within a CRO in a major role, or from a ...

Bachelor's degree in Life Sciences, Pharmacy or related field (required). * Advanced degree, e.g ... Knowledge of trial risk assessment and management. * Familiarity with clinical trial systems (e.g ...

next page

Showing results 1-20

Trial Science information

See salary details

$11

$37

$68

How much do trial science jobs pay per hour?

As of Jun 14, 2026, the average hourly pay for trial science in the United States is $37.67, according to ZipRecruiter salary data. Most workers in this role earn between $25.72 and $48.08 per hour, depending on experience, location, and employer.

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 data, and use statistical tools to interpret results, ensuring trials comply with industry standards. Strong knowledge of biology, data analysis, and regulatory requirements is essential for this role.

What jobs pay $500,000 a year in the US?

In the field of trial science, high-paying roles such as senior clinical trial managers, directors of clinical operations, or chief scientific officers can reach or exceed $500,000 annually, especially in large pharmaceutical or biotech companies. These positions typically require extensive experience, advanced degrees, and strong leadership skills, often involving overseeing multiple trials and teams. Compensation may include base salary, bonuses, and stock options.

What is a Trial Science job?

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 job makes $10,000 a month without a degree?

In trial science or related research roles, high-paying positions often require specialized skills, experience, or certifications rather than formal degrees. Some roles in clinical research, pharmaceutical testing, or biotech may offer substantial salaries for experienced professionals, but reaching $10,000 a month typically involves advanced expertise, industry experience, or working in high-demand environments. Entry-level positions generally do not offer such high monthly earnings without relevant qualifications.

What jobs pay $2000 a day?

In trial science or clinical research, highly specialized roles such as senior clinical trial consultants, principal investigators, or contract research organization (CRO) directors can earn around $2,000 per day, especially when working on large-scale or high-stakes trials. These positions typically require advanced degrees, extensive experience, and often involve consulting or contract work with flexible schedules.

What are the key skills and qualifications needed to thrive in the Trial Science position, and why are they important?

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.

What does a typical project workflow look like for a professional in Trial Science?

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.

More about Trial Science jobs
What cities are hiring for Trial Science jobs? Cities with the most Trial Science job openings:
What states have the most Trial Science jobs? States with the most job openings for Trial Science jobs include:
Infographic showing various Trial Science job openings in the United States as of June 2026, with employment types broken down into 76% Full Time, and 24% Part Time. Highlights an 70% Physical, 6% Hybrid, and 24% Remote job distribution, with an average salary of $78,347 per year, or $37.7 per hour.
Clinical Trial Manager/Senior Clinical Trial Manager

Clinical Trial Manager/Senior Clinical Trial Manager

Lexeo Therapeutics

New York, NY • Hybrid

$143K - $180K/yr

Full-time

Posted 25 days ago


Job description

Role Summary 

The Clinical Trial Manager (CTM) or Senior Clinical Trial Manager (Sr. CTM) leads the execution of global clinical studies from startup through close-out. The CTM/Sr. CTM partners closely with cross-functional teams and external vendors to deliver high-quality clinical trials on time and within budget while ensuring compliance with regulatory standards. The CTM will independently manage study execution, while the Sr. CTM will lead more complex programs with broader strategic and cross-functional responsibilities. 

Primary Responsibilities

Clinical Trial Execution

  • Lead day-to-day management of clinical studies to ensure delivery against timelines, budget, and quality expectations
  • Drive study milestones and proactively identify and mitigate risks 

Vendor & CRO Management

  • Oversee CROs, laboratories, and vendors to ensure performance aligns with scope, timelines, and budget
  • Manage vendor relationships, including scope changes, issue resolution, and ongoing performance oversight 

Cross-Functional Collaboration

  • Partner with internal stakeholders across Clinical, Regulatory, Data Management, and other functions
  • Serve as a central operational lead to ensure alignment and efficient study execution 

Study Planning & Strategy

  • Contribute to study planning, including timelines, resource plans, budgets, and risk management strategies
  • Provide operational input into protocol development, feasibility, and study design 

Site & Study Oversight

  • Act as the primary sponsor contact for study sites
  • Oversee site startup and ongoing site management activities
  • Ensure proper sample handling, data flow, and protocol adherence 

Quality & Compliance

  • Ensure compliance with ICH/GCP, FDA regulations, and company SOPs
  • Maintain inspection readiness and support audits and regulatory inspections
  • Ensure completeness and integrity of the Trial Master File (TMF) 

Documentation & Communication

  • Author and review study plans, operational documents, and training materials
  • Communicate study status, risks, and mitigation plans to stakeholders 

Continuous Improvement

  • Contribute to process improvements and operational excellence initiatives
  • (Sr. CTM) Lead cross-study or departmental initiatives 
Required Skills and Qualifications
  • Bachelor's degree in life sciences or a related field; advanced degree preferred
  • Clinical Trial Manager: minimum 7 years of clinical research experience; 4 years with advanced degree
  • Senior Clinical Trial Manager: experience leading complex or global studies, worked on a clinical study from concept to database lock
  • Strong knowledge of ICH/GCP, FDA regulations, and clinical trial operations
  • Experience managing CROs and other external vendors
  • Proven ability to manage timelines, budgets, and multiple priorities
  • Excellent communication, problem-solving, and leadership skills
  • Demonstrated leadership skills
  • Ability to work effectively in a fast-paced, collaborative environment
  • Ability to travel to sites as needed, including international travel
  • Ability to work Eastern Time Zone and travel to New York HQ quarterly 
$143,350 - $180,000 a year
Compensation is dependent on qualifications and experience

About Lexeo 

Lexeo Therapeutics is a clinical-stage genetic medicine company headquartered in New York City, pioneering cardiac genetic medicine candidates to treat the root causes of inherited cardiovascular diseases. Our lead program, LX2006, targets cardiomyopathy associated with Friedreich's Ataxia and anchors a broader pipeline addressing genetically defined conditions such as hypertrophic and arrhythmogenic cardiomyopathies. Backed by a strong financial foundation, Lexeo is positioned to translate groundbreaking science into durable clinical impact. 

Our work culture is a hybrid model with 2 days/week in the New York City office and 3 days working from home.

Lexeo Therapeutics is an EEO employer committed to an exciting, diverse, and enriching work environment. 

We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.
apply for this job