Clinical Research Assistant
$19 - $33/hr
How This Role Makes a Difference The Clinical Research Assistant is an entry level clinical position and is designed to fully integrate the individual in the Care Access Research process while ...
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$19 - $33/hr
How This Role Makes a Difference The Clinical Research Assistant is an entry level clinical position and is designed to fully integrate the individual in the Care Access Research process while ...
Quick apply
$19 - $33/hr
How This Role Makes a Difference The Clinical Research Assistant is an entry level clinical position and is designed to fully integrate the individual in the Care Access Research process while ...
Houston, TX · On-site
$19 - $33/hr
How This Role Makes a Difference The Clinical Research Assistant is an entry level clinical position and is designed to fully integrate the individual in the Care Access Research process while ...
Houston, TX · On-site
$19 - $33/hr
How This Role Makes a Difference The Clinical Research Assistant is an entry level clinical position and is designed to fully integrate the individual in the Care Access Research process while ...
$19 - $33/hr
How This Role Makes a Difference The Clinical Research Assistant is an entry level clinical position and is designed to fully integrate the individual in the Care Access Research process while ...
$19 - $33/hr
How This Role Makes a Difference The Clinical Research Assistant is an entry level clinical position and is designed to fully integrate the individual in the Care Access Research process while ...
$18.25 - $25.25/hr
Research Assistant The Research Assistant will be responsible for assisting the clinical research staff in conducting clinical research trials. DUTIES amp; RESPONSIBILITIES: * Completing DMCR ...
$18.25 - $25.25/hr
Research Assistant The Research Assistant will be responsible for assisting the clinical research staff in conducting clinical research trials. DUTIES amp; RESPONSIBILITIES: * Completing DMCR ...
Clinical Research & Participant Support: Assist with participant recruitment, pre-screening, scheduling, informed consent (under CRC direction), study visits, and maintain positive participant ...
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Clinical Research & Participant Support: Assist with participant recruitment, pre-screening, scheduling, informed consent (under CRC direction), study visits, and maintain positive participant ...
Clinical Research & Participant Support: Assist with participant recruitment, pre-screening, scheduling, informed consent (under CRC direction), study visits, and maintain positive participant ...
Clinical Research & Participant Support: Assist with participant recruitment, pre-screening, scheduling, informed consent (under CRC direction), study visits, and maintain positive participant ...
Prepare visit-specific documentation and charts for Clinical Research Coordinator * Inform subjects and obtain written consent in regard to ICF's * Assist Coordinator in patient care and management ...
Prepare visit-specific documentation and charts for Clinical Research Coordinator * Inform subjects and obtain written consent in regard to ICF's * Assist Coordinator in patient care and management ...
Prepare visit-specific documentation and charts for Clinical Research Coordinator * Inform subjects and obtain written consent in regard to ICF's * Assist Coordinator in patient care and management ...
Prepare visit-specific documentation and charts for Clinical Research Coordinator * Inform subjects and obtain written consent in regard to ICF's * Assist Coordinator in patient care and management ...
Katy, TX · On-site
$19/hr
Prepare visit-specific documentation and charts for Clinical Research Coordinator * Inform subjects and obtain written consent in regard to ICF's * Assist Coordinator in patient care and management ...
Katy, TX · On-site
$19/hr
Prepare visit-specific documentation and charts for Clinical Research Coordinator * Inform subjects and obtain written consent in regard to ICF's * Assist Coordinator in patient care and management ...
Prepare visit-specific documentation and charts for Clinical Research Coordinator * Inform subjects and obtain written consent in regard to ICF's * Assist Coordinator in patient care and management ...
Prepare visit-specific documentation and charts for Clinical Research Coordinator * Inform subjects and obtain written consent in regard to ICF's * Assist Coordinator in patient care and management ...
Katy, TX · On-site
$19/hr
Prepare visit-specific documentation and charts for Clinical Research Coordinator * Inform subjects and obtain written consent in regard to ICF's * Assist Coordinator in patient care and management ...
Katy, TX · On-site
$19/hr
Prepare visit-specific documentation and charts for Clinical Research Coordinator * Inform subjects and obtain written consent in regard to ICF's * Assist Coordinator in patient care and management ...
Prepare visit-specific documentation and charts for Clinical Research Coordinator * Inform subjects and obtain written consent in regard to ICF's * Assist Coordinator in patient care and management ...
Prepare visit-specific documentation and charts for Clinical Research Coordinator * Inform subjects and obtain written consent in regard to ICF's * Assist Coordinator in patient care and management ...
Bellaire, TX · On-site
$19/hr
Prepare visit-specific documentation and charts for Clinical Research Coordinator * Inform subjects and obtain written consent in regard to ICF's * Assist Coordinator in patient care and management ...
Bellaire, TX · On-site
$19/hr
Prepare visit-specific documentation and charts for Clinical Research Coordinator * Inform subjects and obtain written consent in regard to ICF's * Assist Coordinator in patient care and management ...
The Woodlands, TX · On-site
$19/hr
Prepare visit-specific documentation and charts for Clinical Research Coordinator * Inform subjects and obtain written consent in regard to ICF's * Assist Coordinator in patient care and management ...
The Woodlands, TX · On-site
$19/hr
Prepare visit-specific documentation and charts for Clinical Research Coordinator * Inform subjects and obtain written consent in regard to ICF's * Assist Coordinator in patient care and management ...
Prepare visit-specific documentation and charts for Clinical Research Coordinator * Inform subjects and obtain written consent in regard to ICF's * Assist Coordinator in patient care and management ...
Prepare visit-specific documentation and charts for Clinical Research Coordinator * Inform subjects and obtain written consent in regard to ICF's * Assist Coordinator in patient care and management ...
Clinical Research & Participant Support: Assist with participant recruitment, pre-screening, scheduling, informed consent (under CRC direction), study visits, and maintain positive participant ...
Clinical Research & Participant Support: Assist with participant recruitment, pre-screening, scheduling, informed consent (under CRC direction), study visits, and maintain positive participant ...
Bellaire, TX · On-site
$21.75 - $29/hr
Summary: The Clinical Research Coordinator will manage the day-to-day operations of assigned ... Create and maintain reports and/or spreadsheets as requested * Assist regulatory personnel in ...
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Bellaire, TX · On-site
$21.75 - $29/hr
Summary: The Clinical Research Coordinator will manage the day-to-day operations of assigned ... Create and maintain reports and/or spreadsheets as requested * Assist regulatory personnel in ...
$18 - $24/hr
Research Assistant (Lab Technician) DM Clinical Research, the largest privately-owned clinical research organization in the Houston area and one of the top fifty in the country, is looking for an ...
$18 - $24/hr
Research Assistant (Lab Technician) DM Clinical Research, the largest privately-owned clinical research organization in the Houston area and one of the top fifty in the country, is looking for an ...
$21 - $27.75/hr
At least two years of experience as a research assistant, data coordinator, laboratory personnel, or equivalent experience in a clinical research setting Credentials: * ACRP or equivalent ...
$21 - $27.75/hr
At least two years of experience as a research assistant, data coordinator, laboratory personnel, or equivalent experience in a clinical research setting Credentials: * ACRP or equivalent ...
Tomball, TX · On-site
$23 - $30.50/hr
Unblinded Clinical Research Coordinator DM Clinical Research, the largest privately-owned clinical ... Assistant) Knowledge and Skills: * Computer proficiency, especially Word, Excel, Outlook, and ...
Tomball, TX · On-site
$23 - $30.50/hr
Unblinded Clinical Research Coordinator DM Clinical Research, the largest privately-owned clinical ... Assistant) Knowledge and Skills: * Computer proficiency, especially Word, Excel, Outlook, and ...
$7.27 - $10.35
7% of jobs
$10.35 - $13.42
2% of jobs
$15.19 is the 25th percentile. Wages below this are outliers.
$13.42 - $16.49
27% of jobs
The median wage is $18.09 / hr.
$16.49 - $19.56
26% of jobs
$22.02 is the 75th percentile. Wages above this are outliers.
$19.56 - $22.64
16% of jobs
$22.64 - $25.71
9% of jobs
$25.71 - $28.78
7% of jobs
$28.78 - $31.85
4% of jobs
$31.85 - $34.93
1% of jobs
$34.93 - $38
0% of jobs
$38 - $41.07
0% of jobs
$7
$20
$41
A clinical research assistant—or clinical research associate (CRA)—helps lead researchers during clinical trials for new drugs and medical devices. As a clinical research assistant, your responsibilities include preparing the laboratory, processing volunteers, taking biological samples or vital signs, and organizing data. You may also be required to set up and clean work areas. Your job is to assist the researchers in any way possible, helping them conduct sound, ethical, and scientifically accurate research.
| Aspect | Clinical Research Assistant | Clinical Research Coordinator |
|---|---|---|
| Credentials | Typically requires a bachelor's degree in health sciences or related field; certifications like CCRP are a plus | Requires a bachelor's degree; certifications such as CCRP or CCRC are common |
| Work Environment | Assists in data collection, patient scheduling, and administrative tasks in clinical trial settings | Manages study protocols, patient recruitment, and regulatory compliance in clinical trial sites |
| Employer & Industry | Hospitals, research institutions, pharmaceutical companies | Hospitals, research centers, pharmaceutical companies |
Both roles support clinical research but differ in responsibilities. Clinical Research Assistants focus on data collection and administrative tasks, while Clinical Research Coordinators oversee study management and patient interactions. Understanding these differences helps in choosing the right career path or job search focus.

$19 - $33/hr
Full-time
Medical, Dental, Vision, Retirement, PTO
Posted 5 days ago
About Care Access
Care Access is working to make the future of health better for all. With hundreds of research locations, mobile clinics, and clinicians across the globe, we bring world-class research and health services directly to communities that often face barriers to care. We are dedicated to ensuring that every person has the opportunity to understand their health, access the care they need, and contribute to the medical breakthroughs of tomorrow.
With programs like Future of Medicine, which makes advanced health screenings and research opportunities accessible to communities worldwide, and Difference Makers, which supports local leaders to expand their community health and wellbeing efforts, we put people at the heart of medical progress. Through partnerships, technology, and perseverance, we are reimagining how clinical research and health services reach the world. Together, we are building a future of health that is better and more accessible for all.
To learn more about Care Access, visit www.CareAccess.com.
The Clinical Research Assistant is an entry level clinical position and is designed to fully integrate the individual in the Care Access Research process while learning the skills necessary to be a Clinical Research Coordinator. This position has potential growth and advancement within the Care Access Research organization.
The expected pay range for this role is $19.00 - $33.00 USD per hour for full time team members.
Benefits & Perks (US Full Time Employees)Mandatory Employer Disclosures:
Notice to Illinois applicants: Applicants are not obligated to disclose expunged juvenile records or adjudication, arrest, or conviction.
Notice to Connecticut applicants: Care Access may require applicants to submit to a urinalysis drug test in connection with an application for employment.
Notice to Arizona, Georgia, Indiana, and North Dakota applicants: Care Access complies with applicable laws prohibiting smoking in and around places of employment.
Notice to Massachusetts applicants: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.
Notice to Rhode Island applicants: Care Access complies with Rhode Island law prohibiting smoking in enclosed areas within places of employment. Care Access is also subject to is subject to Chapters 29–38 of Title 28 of the Rhode Island General Laws.
Notice to Maryland applicants: UNDER MARYLAND LAW, AN EMPLOYER MAY NOT REQUIRE OR DEMAND, AS A CONDITION OF EMPLOYMENT, PROSPECTIVE EMPLOYMENT, OR CONTINUED EMPLOYMENT, THAT AN INDIVIDUAL SUBMIT TO OR TAKE A LIE DETECTOR OR SIMILAR TEST. AN EMPLOYER WHO VIOLATES THIS LAW IS GUILTY OF A MISDEMEANOR AND SUBJECT TO A FINE NOT EXCEEDING $100.
Diversity & Inclusion
We work with and serve people from diverse cultures and communities around the world. We are stronger and better when we build a team representing the communities we support. We maintain an inclusive culture where people from a broad range of backgrounds feel valued and respected as they contribute to our mission.
We are an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to, and will not be discriminated against on the basis of, race, color, religion, sex, sexual orientation, gender identity or expression, pregnancy, age, national origin, disability status, genetic information, protected veteran status, or any other characteristic protected by law.
Care Access is unable to sponsor work visas at this time.
If you need an accommodation to apply for a role with Care Access, please reach out to: TalentAcquisition@careaccess.com
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Scientific research and development services
501 - 1,000 Employees
Boston, MA, US
2001