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$49K

$107.3K

$189K

How much do clinical research jobs pay per year?

As of Jul 3, 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 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 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 is the starting salary in clinical research?

The starting salary for a clinical research associate or coordinator typically ranges from $50,000 to $65,000 annually, depending on location, education, and experience. Entry-level roles often require knowledge of Good Clinical Practice (GCP) and familiarity with clinical trial management systems.

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, often followed by a master's or doctoral degree for advanced roles. Gaining experience in clinical settings, understanding regulatory requirements, and obtaining certifications like the Certified Clinical Research Professional (CCRP) can enhance job prospects.

Which clinical research jobs pay the most?

Senior roles in clinical research, such as Clinical Project Managers, Clinical Directors, and Principal Investigators, tend to have the highest salaries. These positions often require extensive experience, advanced degrees, and certifications like CCRP or RAC, and they typically involve overseeing multiple studies or teams in a regulatory-compliant environment.

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 regulations, and often work with clinical trial participants, using tools like electronic data capture systems. Strong attention to detail and knowledge of Good Clinical Practice (GCP) are essential.

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.

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.
More about Clinical Research jobs
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:
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What job categories do people searching Clinical Research jobs look for? The top searched job categories for Clinical Research jobs are:
Clinical Research jobs near you
Infographic showing various Clinical Research job openings in the United States as of June 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $107,336 per year, or $51.6 per hour.

Clinical Research Coordinator

Clinical Research Solution

Cypress, TX • On-site

$21 - $27.75/hr

Other

This job post has expired today. Applications are no longer accepted.

Job description

Company Description Clinical Research Solution is a Site Management Organization focused on optimizing clinical research operations and improving patient outcomes. The company streamlines the complexities of clinical trials by offering innovative solutions that enhance efficiency, compliance, and data quality. Working closely with research sites, sponsors, and CROs, Clinical Research Solution supports study management, patient recruitment, and regulatory adherence. By combining cutting-edge technology with deep industry expertise, the organization enables healthcare professionals to conduct high-quality research and accelerate the development of life-changing treatments. A strong commitment to collaboration, robust data management, and a patient-centric approach drives all aspects of the company’s work.

Role Description This is a full-time, on-site Clinical Research Coordinator role based in Cypress, TX. The Clinical Research Coordinator will manage day-to-day clinical trial activities, including scheduling and coordinating participant visits, preparing study materials, and maintaining accurate source documents and case report forms. This role will support investigators in implementing study protocols, ensure timely collection and entry of study data, and monitor adherence to regulatory and sponsor requirements. The coordinator will facilitate the informed consent process, maintain communication with study participants, and address questions or concerns in a professional and compassionate manner. Additional responsibilities include coordinating with sponsors and CROs, preparing for monitoring visits and audits, managing investigational product accountability as applicable, and contributing to continuous improvement of site processes.

Qualifications


  • Clinical research foundations: Strong understanding of clinical research principles, including Research methods and experience with Clinical Trials.
  • Study conduct and protocol adherence: Demonstrated Clinical Research Experience with implementing and following Protocol requirements in a regulated environment.
  • Participant safety and ethics: Proficiency in conducting and documenting the Informed Consent process in accordance with ethical and regulatory standards.
  • Data and documentation: Ability to maintain accurate source documents, perform timely data entry, and ensure data integrity and confidentiality.
  • Communication and collaboration: Effective written and verbal communication skills, with the ability to work closely with investigators, participants, sponsors, and CROs.
  • Organizational skills: Strong attention to detail, time management, and the ability to manage multiple studies or tasks in a fast-paced environment.
  • Education and credentials: Bachelor’s degree in a health-related, science, or related field preferred; certification as a Clinical Research Coordinator (e.g., ACRP, SOCRA) is a plus.
  • Experience: Prior on-site clinical research coordination experience in outpatient or site-based settings strongly preferred; familiarity with electronic data capture and site management systems is beneficial.

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