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$49K

$107.3K

$189K

How much do clinical research jobs pay per year?

As of Jun 12, 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 does a clinical researcher do?

A clinical researcher designs and conducts studies to evaluate the safety and effectiveness of medical treatments, drugs, or devices. They collect and analyze data, ensure compliance with regulatory standards, and often work in hospitals, research institutions, or pharmaceutical companies, using tools like electronic data capture systems. Strong analytical skills and knowledge of Good Clinical Practice (GCP) are essential for this role.

How much does a CRC make?

A Clinical Research Coordinator (CRC) in Houston typically earns between $50,000 and $70,000 annually, depending on experience, certifications, and the complexity of clinical trials. Entry-level CRCs may start around $45,000, while experienced coordinators with certifications like CCRP can earn higher salaries. The role often requires strong organizational skills and knowledge of regulatory requirements.

Can you be a CRA with no experience?

A Clinical Research Associate (CRA) typically requires some prior knowledge of clinical trials, regulations, and monitoring procedures. While entry-level positions may be available, most employers prefer candidates with related experience or relevant certifications, such as a CRA training program or a background in healthcare or life sciences. Gaining experience through internships or entry-level roles can improve chances of becoming a CRA without prior direct experience.

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 are careers in clinical research?

Careers in clinical research involve designing, conducting, and managing clinical trials to evaluate new medical treatments and devices. Roles include clinical research coordinators, clinical data managers, and regulatory affairs specialists, often requiring knowledge of Good Clinical Practice (GCP) and relevant certifications. These jobs are typically based in healthcare or pharmaceutical settings and may require strong organizational and communication skills.

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:
What states have the most Clinical Research jobs? States with the most job openings for Clinical Research jobs include:
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 1% Locum Tenens, 4% As Needed, 68% Full Time, 18% Part Time, and 9% Contract. Highlights an 89% Physical, 3% Hybrid, and 8% Remote job distribution, with an average salary of $107,336 per year, or $51.6 per hour.
Clinical Research Assistant

Clinical Research Assistant

Tandem Clinical Research

Marrero, LA • On-site

Full-time

Posted 22 days ago

Job description

The Clinical Research Assistant (CRA) assists in the daily activities of clinical research studies and clinic operations. This role involves working closely with clinical teams, investigators, and study participants to ensure that all required procedures and visits occur according to protocol-specific guidelines.
Key Responsibilities:
  • Study Familiarization: Thoroughly understand assigned studies by reading protocols, attending start-up meetings, and coordinating with the Principal Investigator and study team.
  • Protocol Adherence: Ensure strict adherence to study protocols and obtain exemptions when applicable.
  • Specimen Collection & Processing: Collect, process, and ship laboratory samples in accordance with study requirements.
  • Patient Screening & Qualification: Collect initial psychiatric and medical information through patient interviews and access appropriate sources to qualify and accurately place patients in enrolling clinical trials.
  • Study Coordination Support: Assist Clinical Research Coordinators in trial-related organization and documentation, including filing and maintaining regulatory records.
  • Communication & Reporting: Communicate protocol issues to the study team, Site Administrator, Principal Investigator (PI), or Sub-Investigator as needed.
  • Clinical Tasks: Perform clinical tasks such as vital signs measurement, height and weight recording, ECG administration, phlebotomy, and specimen packaging.
  • Documentation & Compliance: Maintain timely source documentation and ensure compliance with sponsor-required information.
  • Patient Education: Educate patients and their families about study participation and clinical drug trials in general.
  • Community Engagement: Assist in community outreach events and provide appropriate community resource referrals to patients, caretakers, and family members when applicable.
  • Additional Duties: Perform ad-hoc tasks and assist in other study-related activities as needed.

Additional Responsibilities:
This job description outlines the primary responsibilities of the Clinical Research Assistant; however, additional duties may be assigned as needed to support the research program or the operational needs of the organization. These additional responsibilities are not limited to the above and may evolve over time based on study requirements or business needs.
Requirements
Knowledge, Skills, and Abilities:
  • Communication: Ability to communicate effectively (both written and oral) with patients, study teams, and external stakeholders.
  • Interpersonal Skills: Excellent interpersonal and customer service skills to engage with study participants and colleagues.
  • Organizational Skills: Strong ability to prioritize tasks, manage multiple responsibilities, and maintain documentation.
  • Technical Proficiency: Proficiency in Microsoft Office software required; knowledge of Electronic Medical Records (EMR) systems preferred.
  • Attention to Detail: High level of accuracy in maintaining documentation and following protocol guidelines.
  • Team Collaboration: Ability to work independently and collaboratively within a multidisciplinary team.
  • Confidentiality: Ability to handle sensitive participant data while adhering to ethical and regulatory guidelines.

Required Experience and Qualifications:
  • Education: Bachelor's degree preferred.
  • Experience: Previous experience in a healthcare or clinical research setting is a plus.
  • Clinical Trials Knowledge: Previous exposure to clinical trials is preferred but not required.

This role is ideal for someone detail-oriented, organized, and eager to support clinical research in advancing medical knowledge and patient care.

Apply