Clinical Research Assistant Jobs in Memphis, TN
Clinical Research Assistant jobs in Memphis are concentrated in the Medical District around the University of Tennessee Health Science Center, St. Jude Children's Research Hospital corridor, and East Memphis, with strong demand in oncology, infectious disease, and clinical trials management. Top employers hiring right now include St. Jude Children's Research Hospital, CNS Healthcare, and Iterative Health. See the openings below and apply to the ones that match your experience.
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Showing 5 of 32+ Clinical Research Assistant jobs
Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes.
We built a leading performance-driven network of 100+ sites across the US, Europe, India, and Australia, conducting research directly in the communities where care is delivered across gastrointestinal, hepatology, obesity, and cardiology. By combining deep clinical trial expertise with cutting-edge AI, we connect sponsors' scientific ambitions with high-performing research teams that expedite and expand access to novel therapeutics for patients in need. Today, Iterative Health is headquartered in Cambridge, Massachusetts, and New York City with 250+ employees world-wide.
As a Clinical Research Coordinator I (CRC I) at Iterative Health you will play an important role in the successful execution of clinical trials and the overall patient research experience. This role supports the coordination of day-to-day study activities while ensuring compliance with protocol requirements, regulatory standards, and patient safety guidelines.
The CRC I works closely with patients, sponsors, CROs, investigators, and internal teams to help deliver high-quality clinical research and contribute to the advancement of innovative therapies.
Where You'll Drive Impact
- Support the coordination and execution of industry-sponsored clinical trials under the guidance of site leadership and senior research staff
- Coordinate patient visits, procedures, and study-related activities in accordance with protocol requirements and study timelines
- Support patient recruitment and retention activities including chart review, patient outreach, scheduling, and informed consent coordination
- Conduct protocol-required patient visits and assessments in accordance with study protocols, GCP guidelines, and site SOPs
- Perform protocol-required clinical procedures including vital signs, ECGs, specimen collection, and investigational product accountability, as permitted by applicable regulations, training, and organizational policy
- Process laboratory specimens and prepare shipments in accordance with protocol requirements and applicable IATA regulations
- Maintain accurate and timely study documentation including source records, informed consent forms, CTMS updates, and case report forms
- Ensure high-quality data entry and support timely resolution of data queries
- Serve as a point of contact for study participants throughout study participation
- Maintain ongoing communication with sponsors, CROs, investigators, and internal site teams to support study execution
- Support preparation for sponsor, CRO, and regulatory monitoring visits
- Maintain inventory and organization of study equipment, supplies, and investigational products
- Support the protection of human research participants in compliance with federal regulations, GCP, HIPAA, and institutional policies
- Maintain compliance with all site SOPs, privacy standards, and research protocols
- Perform job related duties as requested
What You Bring to the Team
- Associate's or Bachelor's degree in a scientific, healthcare, or related discipline required
- 1–3 years of clinical research or healthcare experience required
- Must be able to perform blood draw, medical review (blood pressure, height, weight etc.) & EKGs, as applicable by state law
- Strong organizational skills and attention to detail
- Ability to manage competing priorities in a fast-paced environment
- Ability to read, interpret, and apply research protocols and clinic policies
- Proficiency with standard office software and willingness to learn clinical research systems
- Familiarity with CTMS or EDC systems preferred
Physical Requirements
- Ability to sit, stand, and move throughout clinical and office environments for extended periods of time
- Ability to lift and move up to 25 pounds as needed
At Iterative Health, we're actively working towards creating an environment that is representative of the diversity of patients our technology serves. We are focused on building an equitable and inclusive culture, and by extension, hiring process. If you require any accommodations to make the application process or interviewing experience more accessible to you, please contact CandidateAccommodations@iterative.health.
Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes.
We built a leading performance-driven network of 100+ sites across the US, Europe, India, and Australia, conducting research directly in the communities where care is delivered across gastrointestinal, hepatology, obesity, and cardiology. By combining deep clinical trial expertise with cutting-edge AI, we connect sponsors' scientific ambitions with high-performing research teams that expedite and expand access to novel therapeutics for patients in need. Today, Iterative Health is headquartered in Cambridge, Massachusetts, and New York City with 250+ employees world-wide.
As a Clinical Research Coordinator I (CRC I) at Iterative Health you will play an important role in the successful execution of clinical trials and the overall patient research experience. This role supports the coordination of day-to-day study activities while ensuring compliance with protocol requirements, regulatory standards, and patient safety guidelines.
The CRC I works closely with patients, sponsors, CROs, investigators, and internal teams to help deliver high-quality clinical research and contribute to the advancement of innovative therapies.
Where You'll Drive Impact
- Support the coordination and execution of industry-sponsored clinical trials under the guidance of site leadership and senior research staff
- Coordinate patient visits, procedures, and study-related activities in accordance with protocol requirements and study timelines
- Support patient recruitment and retention activities including chart review, patient outreach, scheduling, and informed consent coordination
- Conduct protocol-required patient visits and assessments in accordance with study protocols, GCP guidelines, and site SOPs
- Perform protocol-required clinical procedures including vital signs, ECGs, specimen collection, and investigational product accountability, as permitted by applicable regulations, training, and organizational policy
- Process laboratory specimens and prepare shipments in accordance with protocol requirements and applicable IATA regulations
- Maintain accurate and timely study documentation including source records, informed consent forms, CTMS updates, and case report forms
- Ensure high-quality data entry and support timely resolution of data queries
- Serve as a point of contact for study participants throughout study participation
- Maintain ongoing communication with sponsors, CROs, investigators, and internal site teams to support study execution
- Support preparation for sponsor, CRO, and regulatory monitoring visits
- Maintain inventory and organization of study equipment, supplies, and investigational products
- Support the protection of human research participants in compliance with federal regulations, GCP, HIPAA, and institutional policies
- Maintain compliance with all site SOPs, privacy standards, and research protocols
- Perform job related duties as requested
What You Bring to the Team
- Associate's or Bachelor's degree in a scientific, healthcare, or related discipline required
- 1–3 years of clinical research or healthcare experience required
- Must be able to perform blood draw, medical review (blood pressure, height, weight etc.) & EKGs, as applicable by state law
- Strong organizational skills and attention to detail
- Ability to manage competing priorities in a fast-paced environment
- Ability to read, interpret, and apply research protocols and clinic policies
- Proficiency with standard office software and willingness to learn clinical research systems
- Familiarity with CTMS or EDC systems preferred
Physical Requirements
- Ability to sit, stand, and move throughout clinical and office environments for extended periods of time
- Ability to lift and move up to 25 pounds as needed
At Iterative Health, we're actively working towards creating an environment that is representative of the diversity of patients our technology serves. We are focused on building an equitable and inclusive culture, and by extension, hiring process. If you require any accommodations to make the application process or interviewing experience more accessible to you, please contact CandidateAccommodations@iterative.health.
See All 32 Clinical Research Assistant Jobs in Memphis
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Find JobsClinical Research Assistant Job Market in Memphis
Who's Hiring
- St. Jude Children's Research Hospital11
- CNS Healthcare5
- Iterative Health5
- West Cancer Center5
- Alcanza Clinical Research5
Clinical Research Assistant Jobs in Memphis: Frequently Asked Questions
How do I get a clinical research assistant job in Memphis?
Focus your search on Memphis's Medical District, where academic medical centers, pediatric research institutions, and contract research organizations concentrate most openings. Candidates with hands-on patient contact experience, familiarity with IRB protocols, and exposure to oncology or infectious disease trials stand out locally. Networking through the University of Tennessee Health Science Center and Memphis-area hospital systems also opens doors that general job searches miss.
Which companies hire clinical research assistants in Memphis?
Memphis clinical research assistant roles are posted by St. Jude Children's Research Hospital, CNS Healthcare, and Iterative Health and others right now, based on current listings on Migrate Mate as of September 2026. Memphis employers tend to include large academic medical centers, pediatric specialty hospitals, and CRO satellite offices serving the Mid-South region.
Are there remote clinical research assistant jobs in Memphis?
Yes, but with limits since most clinical research assistant work requires on-site patient interaction, specimen handling, or direct trial coordination. About 0% of clinical research assistant openings tied to Memphis are remote or hybrid as of September 2026, which skews toward data entry, regulatory document management, and sponsor communication roles rather than hands-on study coordination.
How can I get a clinical research assistant job in Memphis with little or no experience?
The most realistic entry path in Memphis is through a clinical research coordinator internship or volunteer research position at one of the Medical District's hospital systems or university-affiliated programs. Memphis employers frequently hire entry-level candidates into data entry or patient recruitment roles that transition into full assistant positions. A coursework background in life sciences combined with any clinical exposure, even as a medical scribe or phlebotomist, gives candidates a concrete edge locally.
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