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Clinical Study Associate Jobs in Nebraska (NOW HIRING)

... studies, maintenance and corrective actions, preparing and evaluation of reagents, media, and ... Bachelor's degree in medical technology or chemical, physical, biological sciences or Associates ...

... studies, maintenance and corrective actions, preparing and evaluation of reagents, media, and ... Bachelor's degree in medical technology or chemical, physical, biological sciences or Associates ...

EMG Tech

Omaha, NE · On-site

$21.85 - $30.87/hr

Recognizes clinically significant events and follows facility policy and procedures regarding ... Associates Other Commission on Accreditation of Allied Health education Program (CAAHEP ...

Showing results 41-60

Clinical Study Associate information

See Nebraska salary details

$12

$30

$52

How much do clinical study associate jobs pay per hour?

As of Aug 11, 2026, the average hourly pay for clinical study associate in Nebraska is $30.07, according to ZipRecruiter salary data. Most workers in this role earn between $20.19 and $39.66 per hour, depending on experience, location, and employer.

What is a clinical study associate?

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?

AspectClinical Study AssociateClinical Research Coordinator
CredentialsBachelor's degree, often in life sciences; certifications like CCRP or CCRA beneficialBachelor's degree in health sciences or related field; certifications like CCRP advantageous
Work EnvironmentPharmaceutical companies, CROs, clinical trial sitesHospitals, clinics, research centers
Job FocusMonitoring clinical trials, ensuring protocol compliance, data accuracyManaging daily trial activities, patient recruitment, data collection
Employer & Industry UsageCommonly employed in pharma and CROsPrimarily 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 Nebraska? The most popular types of Clinical Study jobs in Nebraska are:
What cities in Nebraska are hiring for Clinical Study Associate jobs? Cities in Nebraska with the most Clinical Study Associate job openings:
Infographic showing various Clinical Study Associate job openings in Nebraska as of August 2026, with employment types broken down into 2% As Needed, 73% Full Time, 19% Part Time, and 6% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $62,550 per year, or $30.1 per hour.

Clinical Lab Coordinator

Boystown

Omaha, NE • On-site

Full-time

Life, Retirement

Posted 29 days ago


Job description

Business: Boys Town National Research Hospital
Job Summary:
In a career as a Clinical Lab Coordinator, you join us in providing life-changing care to patients from across the region. In this role, you will coordinate day-to-day laboratory operations and ensure quality laboratory service. Regulate the workflow efficiency of the department through formulating daily personnel assignments or adjustments considering staffing levels and the patient's needs.
Schedule: Full time, 730 AM-4:00 PM Monday-Friday with no holidays or weekends.
Location: West HospitalMAJOR RESPONSIBILITIES & DUTIES:
  • Assists in the development of departmental action plans and makes recommendations to the Laboratory Manager for training and staff development.
  • Monitors productivity to assure maximum staff utilization at minimum costs.
  • Provides technical guidance and skill development to assigned staff in all procedures in order to maximize the efficiency and effectiveness of patient care.
  • Follows all laboratory procedures and policies, (quality control, precision, accuracy, and correlation studies, maintenance and corrective actions, preparing and evaluation of reagents, media, and standards) to maximize efficiency and effectiveness of lab services.
  • Demonstrates and maintains competency in all aspects of patient testing including specimen collection, sample processing, test performance and reporting.
  • Monitors daily performance of department quality control, maintenance checklists, and safety policies to ensure completion and accuracy.
  • Maintains communication with Laboratory management as liaison for department employees.
  • Participates in the development and evaluation of new laboratory procedures to maintain current preferred methodologies.
  • Provides training and orientation of new department personnel to ensure consistent application of department procedures and laboratory policies.
  • Performs quality control procedures and laboratory testing of biological fluids on specific laboratory instrumentation according to established protocols. Evaluates results for abnormalities and inconsistencies by following predetermined protocol and take the necessary action to alert the appropriate personnel or correct the malfunctioning instrumentation and document any actions taken.
  • Communicates test results to appropriate personnel and/or clients via verbal, written, or computer link communication in a prompt, professional and courteous manner.
  • Participates in department meetings and Laboratory committee activities to maintain continuity, consistency, and communication inside and outside of the department.
  • Provides patient care and education according to the patient population served.
REQUIRED QUALIFICATIONS:
  • Bachelor's degree in medical technology or chemical, physical, biological sciences or Associates Degree in Medical Laboratory Technician from an accredited college or university required.
  • Minimum of five years of full-time laboratory experience or training in the specialty or sub-specialty in which the individual performs tests required.
  • BLS certification required.
  • Registered by the ASCP or NCA required.

Care and respect for others is more than a commitment at Boys Town - it is the foundation of who we are and what we do.

At Boys Town, we cultivate a culture of belonging for all employees that respects their individual strengths, views, and experiences. We believe that our differences enable us to be a better team - one that makes better decisions, drives innovation, and delivers better business results.

About Boys Town:

Boys Town has been changing the way America cares for children and families since 1917. With over a century of service, our employees have helped us grow from a small boardinghouse in downtown Omaha, Nebraska, into one of the largest national child and family care organizations in the country. With the addition of Boys Town National Research Hospital in 1977, our services branched out into the health care and research fields, offering even more career opportunities to those looking to make a real difference.

Our employees are our #1 supporters when it comes to achieving Boys Town's mission, which is why we are proud of their commitment to making the world a better place for children, families, patients, and communities. A unique feature for employees and their dependents enrolled in medical benefits are reduced to no cost visits for services performed by a Boys Town provider at a Boys Town location. Additional costs savings for the employee and their dependents are found in our pharmacy benefits with low to zero-dollar co-pays on certain maintenance drugs. Boys Town takes your mental health seriously with no cost mental health visits to an in-network provider. We help our employees prepare for retirement with a generous match on their 401K or 401K Roth account. Additional benefits include tuition reimbursement, parenting resources from our experts and professional development opportunities within the organization, just to name a few. Working at Boys Town is more than just a job, it is a way of life.

This advertisement describes the general nature of work to be performed and does not include an exhaustive list of all duties, skills, or abilities required. Boys Town is an equal employment opportunity employer and participates in the E-Verify program. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity and/or expression, national origin, age, disability, or veteran status. To request a disability-related accommodation in the application process, contact us at 1-877-639-6003.