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Horizon Clinical Research

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Clinical Research Assistant

Cypress, TX · On-site

$37K - $47K/yr

We are seeking an experienced and detail oriented Clinical Research Assistant (CRA) for our Cypress, TX and Houston, TX office. This is a full time position. The CRA will work under the supervision ...

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Clinical Research information

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$49K

$107.3K

$189K

How much do clinical research jobs pay per year?

As of Sep 1, 2026, the average yearly pay for clinical research in the United States is $107,336.00, according to ZipRecruiter salary data. Most workers in this role earn between $81,000.00 and $122,500.00 per year, depending on experience, location, and employer.

What is clinical research?

Clinical research is a branch of healthcare science that focuses on studying human health and illness through clinical trials and observational studies. It aims to improve medical knowledge by testing new treatments, drugs, medical devices, or interventions in controlled environments. Clinical research professionals design, conduct, and monitor studies to ensure that data is accurate and that participant safety and ethical standards are maintained. The results of clinical research can lead to new therapies, improved patient care, and informed healthcare policies.

What are different clinical research jobs?

Some of the different types of clinical research jobs include clinical research associates, coordinators, data managers, clinical nurses, research scientists, and biostatisticians. There are also administrative, managerial, and recruitment positions. As a research associate, you monitor the clinical trials and the people administering them, such as clinical nurses and research coordinators who work under the direction of the principal investigator. As a biostatistician, your duties are to collect data about the study and analyze the results to determine if the medication or treatment shows statistically significant effects on participants.

What are the key skills and qualifications needed to thrive in clinical research, and why are they important?

To thrive in Clinical Research, you need a strong background in life sciences, data analysis, and regulatory compliance, often supported by a relevant degree and experience in clinical trials. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and certifications like GCP (Good Clinical Practice) are commonly required. Attention to detail, strong organizational skills, and effective communication make candidates stand out in this field. These skills ensure the integrity of research data, regulatory adherence, and successful collaboration among cross-functional teams.

What are some typical challenges faced by professionals in clinical research, and how can they be managed?

Clinical research professionals often face challenges such as strict regulatory compliance, tight timelines, and coordination among multidisciplinary teams. Managing large volumes of data and ensuring participant safety are also key concerns. Staying organized, maintaining open communication with team members, and keeping updated on regulatory changes can help professionals navigate these challenges effectively. It's also helpful to develop strong project management skills and to build collaborative relationships with investigators, sponsors, and regulatory bodies.

What is the difference between Clinical Research vs Clinical Data Coordinator?

AspectClinical ResearchClinical Data Coordinator
Required CredentialsTypically a bachelor's degree in health sciences, life sciences, or related field; certifications like CCR or CCRA are commonOften a bachelor's degree in health or data management; certifications like CDMP or CCRC may be preferred
Work EnvironmentResearch sites, pharmaceutical companies, CROs, hospitalsClinical trial sites, hospitals, research organizations
Job FocusDesigning, managing, and overseeing clinical trialsManaging and ensuring accuracy of clinical trial data

Clinical Research involves overseeing entire clinical trials, including protocol development and compliance, while Clinical Data Coordinators focus on collecting, managing, and ensuring the quality of trial data. Both roles are essential in the clinical research process but differ in scope and responsibilities.

How do you become a clinical researcher?

To become a clinical researcher, typically a bachelor's degree in a health-related field such as biology, nursing, or medicine is required, followed by relevant experience or advanced education like a master's or PhD. Certification in clinical research, such as the Certified Clinical Research Professional (CCRP), can enhance job prospects. Strong analytical skills, knowledge of regulatory guidelines, and familiarity with research tools are also important.

Is clinical research a good career path?

Clinical research is a viable career that involves managing and conducting trials to test new medical treatments and drugs. It requires strong organizational skills, knowledge of regulatory guidelines, and often a background in healthcare or life sciences. The field offers opportunities for advancement and specialization, with roles in research coordination, data management, and regulatory affairs.

What do you do in a clinical research job?

A clinical research job involves designing, conducting, and managing studies to evaluate the safety and effectiveness of medical treatments or devices. Professionals in this field collect and analyze data, ensure compliance with regulatory standards, and often work with clinical trial participants, using tools like electronic data capture systems. Strong attention to detail, knowledge of Good Clinical Practice (GCP), and relevant certifications are important for success.

What qualifications do you need to be a clinical research professional?

A clinical research professional typically needs a bachelor's degree in a health-related field such as biology, nursing, or pharmacy. Relevant certifications, like the Certified Clinical Research Professional (CCRP), and knowledge of Good Clinical Practice (GCP) guidelines are often required. Strong organizational skills and familiarity with clinical trial management systems are also important.
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What cities are hiring for Clinical Research jobs?

Cities with the most Clinical Research job openings:

What are the most commonly searched types of Clinical Research jobs?

The most popular types of Clinical Research jobs are:

What states have the most Clinical Research jobs?

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What job categories do people searching Clinical Research jobs look for?

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Clinical Research jobs near you
Infographic showing various Clinical Research job openings in the United States as of August 2026, with employment types broken down into 3% As Needed, 71% Full Time, 18% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $107,336 per year, or $51.6 per hour.

Clinical Research Coordinator

FIDES clinical research

Sandy Springs, GA • On-site

$24 - $32/hr

Other

Posted 5 days ago

Job description

Company Description FIDES Clinical Research is a dedicated clinical research organization focused on conducting high-quality clinical trials that advance medical knowledge and improve patient care. The team collaborates with sponsors, healthcare professionals, and participants to ensure studies are conducted ethically, efficiently, and in accordance with regulatory standards. FIDES Clinical Research emphasizes data integrity, participant safety, and clear communication throughout the research process. The organization offers a professional environment where clinical research staff can develop their skills and contribute meaningfully to the progress of new therapies and treatments.
Role Description This is a full-time, on-site Clinical Research Coordinator role based in Sandy Springs, GA. The Clinical Research Coordinator will manage day-to-day study activities, including screening and enrolling participants, scheduling study visits, and maintaining accurate source documentation and case report forms. Responsibilities include coordinating informed consent discussions, ensuring adherence to study protocols, handling regulatory submissions, and maintaining study files. The role involves close collaboration with investigators, sponsors, monitors, and site staff to ensure compliance with Good Clinical Practice (GCP) and institutional policies. The coordinator will also track study timelines, report adverse events, and support data entry, query resolution, and overall study quality.
Qualifications
  • Experience with informed consent processes and participant education, ensuring ethical and compliant enrollment.
  • Strong understanding of study protocols and ability to implement protocol requirements accurately in daily study operations.
  • Solid research skills, including data collection, documentation, and use of electronic data capture systems.
  • Demonstrated clinical research experience, preferably in coordinating clinical trials in outpatient or site-based settings.
  • Familiarity with clinical trials conduct, Good Clinical Practice (GCP), and regulatory guidelines (FDA, IRB).
  • Excellent organizational skills, attention to detail, and ability to manage multiple studies or tasks simultaneously.
  • Effective written and verbal communication skills for interacting with participants, investigators, monitors, and sponsors.
  • Ability to work on-site in Sandy Springs, GA, and collaborate within a multidisciplinary clinical research team.
  • Proficiency in basic computer applications and electronic medical record (EMR) or clinical trial management systems is beneficial.
  • Associate or bachelor’s degree in a health-related field, life sciences, or equivalent experience in clinical research is preferred.

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