Clinical Research Associate Jobs in Memphis, TN
Clinical Research Associate jobs in Memphis are concentrated in the Medical Center district and Midtown corridor, where leading research hospitals and life sciences employers drive consistent demand in oncology, cardiology, and clinical trials management. 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 Associate 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 Associate Jobs in Memphis
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Find JobsClinical Research Associate 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 Associate Jobs in Memphis: Frequently Asked Questions
How do I get a clinical research associate job in Memphis?
Focus on Memphis's Medical Center district, home to a dense cluster of academic medical centers, research hospitals, and specialty clinics that run active clinical trials year-round. Candidates with hands-on trial coordination experience, familiarity with GCP protocols, and exposure to therapeutic areas like oncology or cardiology have a clear edge locally. Networking through the University of Tennessee Health Science Center community also opens doors that posted listings often miss.
Which companies hire clinical research associates in Memphis?
Companies currently hiring clinical research associates in Memphis include St. Jude Children's Research Hospital, CNS Healthcare, and Iterative Health, per current listings on Migrate Mate as of September 2026. Memphis hiring is driven by a mix of academic medical centers, contract research organizations, and specialty hospital systems anchored in and around the Medical Center district.
Are there remote clinical research associate jobs in Memphis?
Yes, though opportunities are limited given that clinical research associate work is largely site-based and requires direct interaction with trial sites and study coordinators. About 0% of clinical research associate openings tied to Memphis are remote or hybrid as of September 2026, reflecting broader industry norms. Data management, regulatory document review, and sponsor-side monitoring roles are most likely to carry remote flexibility in the Memphis market.
How can I get a clinical research associate job in Memphis with little or no experience?
The most realistic entry path in Memphis is through a clinical research coordinator or study coordinator role at one of the Medical Center district's hospital systems or academic research programs, where you build the site-level trial experience employers expect before promoting into a CRA position. Memphis contract research organizations also hire entry-level coordinators for sponsor-delegated tasks. A CCRP or CCRQ certification and any volunteer or internship exposure through UTHSC strengthens your application significantly.
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