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Clinical Research Study Jobs (NOW HIRING)

2505

Clinical Research Coordinator II

Dallas, TX

$24 - $32/hr

Collects and ensures quality control of clinical or basic research data in support of multiple and/or complex research studies. BENEFITS UT Southwestern is proud to offer a competitive and ...

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McLaren

Coordinator Clinical Research

Flint, MI · On-site

$23.50 - $31.25/hr

Responsible for facilitating research studies; providing knowledgeable information regarding each research protocol to the medical and nursing staff; evaluating the eligibility of potential ...

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How much do clinical research study jobs pay per hour?

As of Jul 17, 2026, the average hourly pay for clinical research study in the United States is $24.09, according to ZipRecruiter salary data. Most workers in this role earn between $20.19 and $24.76 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in Clinical Research Studies, and why are they important?

To thrive in clinical research studies, you need a background in life sciences or healthcare, strong analytical skills, and knowledge of research methodologies, often supported by a degree in a related field. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and Good Clinical Practice (GCP) certification is typically required. Attention to detail, strong organizational skills, and effective communication are crucial soft skills for managing protocols, collaborating with teams, and maintaining regulatory compliance. These competencies ensure the integrity of research data, patient safety, and the successful execution of clinical trials.

What qualifications are needed for clinical research?

Clinical research professionals typically need a bachelor's degree in a health-related field such as biology, nursing, or pharmacy. Relevant skills include attention to detail, good communication, and knowledge of Good Clinical Practice (GCP) guidelines; some roles may require certification like the Certified Clinical Research Professional (CCRP).

What are some common challenges faced by professionals working in clinical research studies, and how can they be addressed?

Professionals involved in clinical research studies often face challenges such as patient recruitment, maintaining regulatory compliance, and ensuring accurate data collection. Recruitment can be difficult due to strict inclusion criteria or participant hesitancy, but building partnerships with healthcare providers and clear communication can help. Staying updated on regulatory requirements and utilizing electronic data capture systems can streamline compliance and data accuracy. Effective teamwork and regular communication with investigators, coordinators, and sponsors are essential for addressing these challenges and ensuring study success.

What is a clinical research study?

A clinical research study is a scientific investigation involving human participants, designed to evaluate medical, surgical, or behavioral interventions. These studies help determine the safety and effectiveness of new treatments, drugs, medical devices, or procedures. Clinical research can include clinical trials, observational studies, and longitudinal studies. Participation is usually voluntary, and studies are conducted under strict ethical guidelines to protect participants' rights and safety.

What is the difference between Clinical Research Study and Clinical Research Coordinator?

AspectClinical Research StudyClinical Research Coordinator
RoleParticipates in designing, conducting, and analyzing clinical trialsManages daily trial operations, patient recruitment, and data collection
Required CredentialsOften requires clinical research training, degrees in health sciences, or related certificationsTypically requires similar certifications, with additional experience in patient interaction
Work EnvironmentResearch labs, hospitals, or clinical trial sitesClinical trial sites, hospitals, or research facilities
Employer & Industry UsagePharmaceutical companies, CROs, academic institutionsHospitals, research organizations, pharmaceutical companies

While a Clinical Research Study involves designing and analyzing trials, a Clinical Research Coordinator focuses on managing trial operations and patient interactions. Both roles require similar credentials and work in related environments, but their responsibilities differ significantly.

What are careers in clinical research?

Careers in clinical research include roles such as clinical research coordinators, data managers, clinical trial managers, and research scientists. These positions involve designing, conducting, and monitoring clinical trials to evaluate new medical treatments, often requiring knowledge of Good Clinical Practice (GCP) and relevant certifications. Professionals in this field work in healthcare settings, research institutions, or pharmaceutical companies and typically need strong organizational and communication skills.

What is the highest paying job in clinical research?

The highest paying roles in clinical research are often senior positions such as Clinical Research Vice President or Director, which can earn six-figure salaries. These roles typically require extensive experience, advanced degrees, and strong leadership skills, often overseeing multiple projects or departments.

Is CRA an entry level job?

A Clinical Research Associate (CRA) is typically not an entry-level position; it usually requires prior experience in clinical research, monitoring, or related healthcare fields. Entry-level roles in clinical research may include Clinical Trial Assistants or Coordinators, with CRAs often needing a bachelor's degree and knowledge of Good Clinical Practice (GCP) guidelines.
What cities are hiring for Clinical Research Study jobs? Cities with the most Clinical Research Study job openings:
What are the most commonly searched types of Clinical Research Study jobs? The most popular types of Clinical Research Study jobs are:
Clinical Research Study jobs near you
Clinical Research Assistant

Clinical Research Assistant

Tandem Clinical Research

Houma, LA • On-site

Full-time

Re-posted 27 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.

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