Additionally, the Associate Clinical Research Manager acts as liaison between senior project team members and study subjects. The role involves actively participating and assisting with sponsor ...
Additionally, the Associate Clinical Research Manager acts as liaison between senior project team members and study subjects. The role involves actively participating and assisting with sponsor ...
Additionally, the Associate Clinical Research Manager acts as liaison between senior project team members and study subjects. The role involves actively participating and assisting with sponsor ...
Additionally, the Associate Clinical Research Manager acts as liaison between senior project team members and study subjects. The role involves actively participating and assisting with sponsor ...
Additionally, the Associate Clinical Research Manager acts as liaison between senior project team members and study subjects. The role involves actively participating and assisting with sponsor ...
Additionally, the Associate Clinical Research Manager acts as liaison between senior project team members and study subjects. The role involves actively participating and assisting with sponsor ...
Additionally, the Associate Clinical Research Manager acts as liaison between senior project team members and study subjects. The role involves actively participating and assisting with sponsor ...
Additionally, the Associate Clinical Research Manager acts as liaison between senior project team members and study subjects. The role involves actively participating and assisting with sponsor ...
Additionally, the Associate Clinical Research Manager acts as liaison between senior project team members and study subjects. The role involves actively participating and assisting with sponsor ...
Additionally, the Associate Clinical Research Manager acts as liaison between senior project team members and study subjects. The role involves actively participating and assisting with sponsor ...
Contract Senior Clinical Research Associate - Home-Based (US) ICON is a global healthcare ... Contributing to the preparation and review of study documentation, including protocols and clinical ...
Contract Senior Clinical Research Associate - Home-Based (US) ICON is a global healthcare ... Contributing to the preparation and review of study documentation, including protocols and clinical ...
Contract Senior Clinical Research Associate - Home-Based (US) ICON is a global healthcare ... Contributing to the preparation and review of study documentation, including protocols and clinical ...
Contract Senior Clinical Research Associate - Home-Based (US) ICON is a global healthcare ... Contributing to the preparation and review of study documentation, including protocols and clinical ...
Clinical Research Associate
Austin, TX · On-site
Job Scope The Clinicial Research Associate will be responsible for conducting day-to-day work ... Create clinical study document designs and tracking tools. * Investigate queries, monitor ...
Clinical Research Associate
Austin, TX · On-site
Job Scope The Clinicial Research Associate will be responsible for conducting day-to-day work ... Create clinical study document designs and tracking tools. * Investigate queries, monitor ...
Job Scope The Clinicial Research Associate will be responsible for conducting day-to-day work ... Create clinical study document designs and tracking tools. * Investigate queries, monitor ...
Job Scope The Clinicial Research Associate will be responsible for conducting day-to-day work ... Create clinical study document designs and tracking tools. * Investigate queries, monitor ...
As a Clinical Research Associate (CRA) at Worldwide, you will find yourself working alongside ... Conduct study initiation visits (SIVs) * While most of the site management efforts will be ...
As a Clinical Research Associate (CRA) at Worldwide, you will find yourself working alongside ... Conduct study initiation visits (SIVs) * While most of the site management efforts will be ...
As a Clinical Research Associate (CRA) at Worldwide, you will find yourself working alongside ... Conduct study initiation visits (SIVs) * While most of the site management efforts will be ...
As a Clinical Research Associate (CRA) at Worldwide, you will find yourself working alongside ... Conduct study initiation visits (SIVs) * While most of the site management efforts will be ...
$91K - $114K/yr
Clinical Research Associate - West Coast ICON is a global healthcare intelligence and clinical ... Contributing to the preparation and review of study documentation, including protocols and clinical ...
$91K - $114K/yr
Clinical Research Associate - West Coast ICON is a global healthcare intelligence and clinical ... Contributing to the preparation and review of study documentation, including protocols and clinical ...
Clinical Research Study Manager A Study Manager is responsible to ensure that quality research is ... Working closely with the Associate Site Director/Site Director to achieve strategic goals for the ...
Clinical Research Study Manager A Study Manager is responsible to ensure that quality research is ... Working closely with the Associate Site Director/Site Director to achieve strategic goals for the ...
With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for ... Under the general direction of the Clin Ops Supervisor, the Study Team Associate is responsible for ...
With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for ... Under the general direction of the Clin Ops Supervisor, the Study Team Associate is responsible for ...
With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for ... Under the general direction of the Clin Ops Supervisor, the Study Team Associate is responsible for ...
With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for ... Under the general direction of the Clin Ops Supervisor, the Study Team Associate is responsible for ...
With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for ... Under the general direction of the Clin Ops Supervisor, the Study Team Associate is responsible for ...
With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for ... Under the general direction of the Clin Ops Supervisor, the Study Team Associate is responsible for ...
With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for ... Under the general direction of the Clin Ops Supervisor, the Study Team Associate is responsible for ...
With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for ... Under the general direction of the Clin Ops Supervisor, the Study Team Associate is responsible for ...
This role ensures accurate invoicing, payment tracking, and compliance with study budgets ... Associate's or Bachelor's degree in Accounting, Finance, Healthcare Administration, or related ...
This role ensures accurate invoicing, payment tracking, and compliance with study budgets ... Associate's or Bachelor's degree in Accounting, Finance, Healthcare Administration, or related ...
This role ensures accurate invoicing, payment tracking, and compliance with study budgets ... Associate's or Bachelor's degree in Accounting, Finance, Healthcare Administration, or related ...
Quick apply
This role ensures accurate invoicing, payment tracking, and compliance with study budgets ... Associate's or Bachelor's degree in Accounting, Finance, Healthcare Administration, or related ...
Under general supervision, provides assistance in the negotiation and execution of sponsored research agreement, clinical study agreements, outgoing sub-awards and other agreements. Responsible for ...
Under general supervision, provides assistance in the negotiation and execution of sponsored research agreement, clinical study agreements, outgoing sub-awards and other agreements. Responsible for ...
Clinical Study Associate information
See Texas salary details
$11.87 - $15.47
3% of jobs
$15.47 - $19.08
18% of jobs
$19.79 is the 25th percentile. Wages below this are outliers.
$19.08 - $22.68
20% of jobs
The median wage is $24.87 / hr.
$22.68 - $26.28
15% of jobs
$26.28 - $29.89
11% of jobs
$29.89 - $33.49
4% of jobs
$36.55 is the 75th percentile. Wages above this are outliers.
$33.49 - $37.10
5% of jobs
$37.10 - $40.70
8% of jobs
$40.70 - $44.30
6% of jobs
$44.30 - $47.91
6% of jobs
$47.91 - $51.51
3% of jobs
$11
$29
$51
How much do clinical study associate jobs pay per hour?
As of Jul 24, 2026, the average hourly pay for clinical study associate in Texas is $29.38, according to ZipRecruiter salary data. Most workers in this role earn between $19.71 and $38.75 per hour, depending on experience, location, and employer.
What are Clinical Study Associates?
Clinical Study Associates (CSAs) are professionals who support the planning, execution, and monitoring of clinical trials in the pharmaceutical, biotechnology, or medical device industries. They help coordinate study logistics, maintain study documentation, and ensure compliance with regulatory requirements. CSAs often work closely with Clinical Research Associates, study coordinators, and investigators to ensure that trials are conducted according to protocol and timelines. Their role is essential in ensuring the accuracy and integrity of data collected during clinical research.
What is the difference between Clinical Study Associate vs Clinical Research Coordinator?
| Aspect | Clinical Study Associate | Clinical Research Coordinator |
|---|---|---|
| Credentials | Bachelor's degree, often in life sciences; certifications like CCRP or CCRA beneficial | Bachelor's degree in health sciences or related field; certifications like CCRP advantageous |
| Work Environment | Pharmaceutical companies, CROs, clinical trial sites | Hospitals, clinics, research centers |
| Job Focus | Monitoring clinical trials, ensuring protocol compliance, data accuracy | Managing daily trial activities, patient recruitment, data collection |
| Employer & Industry Usage | Commonly employed in pharma and CROs | Primarily in healthcare and academic research settings |
Both roles involve clinical trial oversight but differ in focus: Clinical Study Associates primarily monitor and ensure compliance during trials, while Clinical Research Coordinators manage daily trial operations and patient interactions. Understanding these distinctions helps in choosing the right career path or job search focus.
What are the key skills and qualifications needed to thrive as a Clinical Study Associate, and why are they important?
To thrive as a Clinical Study Associate, you need a strong understanding of clinical research processes, regulatory requirements, and typically a life sciences degree. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and GCP certification are commonly required. Attention to detail, organizational skills, and effective communication set top performers apart in this role. These competencies ensure accurate study documentation, regulatory compliance, and smooth coordination across research teams.
What are some common challenges Clinical Study Associates face when managing multiple clinical trials simultaneously?
Clinical Study Associates often juggle several clinical trials at once, which can present challenges such as prioritizing competing deadlines, maintaining accurate documentation for each study, and ensuring consistent communication with cross-functional teams. Staying organized and proactive is essential, as unforeseen protocol amendments or site issues can arise. Building strong relationships with site staff and utilizing effective project management tools can help CSAs navigate these complexities and deliver high-quality results.
What are the most commonly searched types of Clinical Study jobs in Texas? The most popular types of Clinical Study jobs in Texas are:
What cities in Texas are hiring for Clinical Study Associate jobs? Cities in Texas with the most Clinical Study Associate job openings:
Full-time
Posted 22 days ago
Thermo Fisher Scientific rating
7.7
Based on 419 frontline employees who took The Breakroom Quiz
201st of 535 rated manufacturers
Job description
Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Office
Job Description
Join Us as an Associate Clinical Research Manager - Make an Impact at the Forefront of Innovation
The Associate Clinical Research Manager assists with managing various aspects of assigned clinical trials involving patient and healthy subject populations in both inpatient and outpatient settings. Additionally, the Associate Clinical Research Manager acts as liaison between senior project team members and study subjects. The role involves actively participating and assisting with sponsor, investigator and research team communications.
What You'll Do:
• Actively participate with senior project team members to meet project needs, projections and deadlines.
• Oversee organization and accuracy of project documents.
• Work with management on understanding departmental needs and improving processes.
• Provide support for the study conduct, working directly with study monitor and study subjects.
• Oversee data entry, source data QC, EDC data entry and EDC query resolution, lab data verification, subject eligibility status review and subject eligibility notification.
Education & Experience Requirements:
• Bachelor's degree or equivalent and relevant formal academic / vocational qualification
• Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 0 to 2 years).
Years of experience refers to typical years of related experience needed to gain the required knowledge, skills, and abilities necessary to perform the essential functions of the job. Years of experience are not to be used as the only determining factor in establishing the job class or making employment selection decisions.
Knowledge, Skills, Abilities:
• Basic knowledge of Phase I processes and clinical study operations
• Fundamental knowledge of FDA regulations and ICH GCP guidelines
• Basic computer skills with working knowledge of Microsoft Office applications
• Time management and multi-tasking skills
• Written and verbal communication skills
• Ability to prioritize workload and adapt to changing study needs
• Ability to act as a liaison between external and internal groups.
Working Conditions and Environment:
• Work is performed in an office/ laboratory and/or a clinical environment.
• Exposure to biological fluids with potential exposure to infectious organisms.
• Exposure to electrical office equipment.
• Personal protective equipment required such as protective eyewear, garments and gloves.
Why Join Us?
When you join Thermo Fisher Scientific, you become part of a global team that values passion, innovation, and a commitment to scientific excellence. You'll work in an environment where collaboration and development are part of the everyday experience-and where your contributions truly make a difference.
Apply today to help us deliver tomorrow's breakthroughs.
Standard (Mon-Fri)
Environmental Conditions
Office
Job Description
Join Us as an Associate Clinical Research Manager - Make an Impact at the Forefront of Innovation
The Associate Clinical Research Manager assists with managing various aspects of assigned clinical trials involving patient and healthy subject populations in both inpatient and outpatient settings. Additionally, the Associate Clinical Research Manager acts as liaison between senior project team members and study subjects. The role involves actively participating and assisting with sponsor, investigator and research team communications.
What You'll Do:
• Actively participate with senior project team members to meet project needs, projections and deadlines.
• Oversee organization and accuracy of project documents.
• Work with management on understanding departmental needs and improving processes.
• Provide support for the study conduct, working directly with study monitor and study subjects.
• Oversee data entry, source data QC, EDC data entry and EDC query resolution, lab data verification, subject eligibility status review and subject eligibility notification.
Education & Experience Requirements:
• Bachelor's degree or equivalent and relevant formal academic / vocational qualification
• Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 0 to 2 years).
Years of experience refers to typical years of related experience needed to gain the required knowledge, skills, and abilities necessary to perform the essential functions of the job. Years of experience are not to be used as the only determining factor in establishing the job class or making employment selection decisions.
Knowledge, Skills, Abilities:
• Basic knowledge of Phase I processes and clinical study operations
• Fundamental knowledge of FDA regulations and ICH GCP guidelines
• Basic computer skills with working knowledge of Microsoft Office applications
• Time management and multi-tasking skills
• Written and verbal communication skills
• Ability to prioritize workload and adapt to changing study needs
• Ability to act as a liaison between external and internal groups.
Working Conditions and Environment:
• Work is performed in an office/ laboratory and/or a clinical environment.
• Exposure to biological fluids with potential exposure to infectious organisms.
• Exposure to electrical office equipment.
• Personal protective equipment required such as protective eyewear, garments and gloves.
Why Join Us?
When you join Thermo Fisher Scientific, you become part of a global team that values passion, innovation, and a commitment to scientific excellence. You'll work in an environment where collaboration and development are part of the everyday experience-and where your contributions truly make a difference.
Apply today to help us deliver tomorrow's breakthroughs.
What Thermo Fisher Scientific employees say
Pay
Benefits
Hours and flexibility
Workplace
Get the full story on Breakroom
About Thermo Fisher Scientific
Sourced by ZipRecruiter
Industry
Biotechnology research and development
Company size
10,000+ Employees
Headquarters location
Waltham, MA, US
Year founded
1956