Top 14 research coordinator Jobs in memphis tn

Clinical Research Coordinator
The Specialty Alliance —Germantown, TN
- $50,000 - $75,000 a year
- Full-time
- Management
- Patient monitoring
- HIPAA
Quick Apply
Program Coordinator - Cancer Predisposition
St. Jude Children's Research Hospital —Memphis, TN
- $70,720 - $126,880 a year
- Full-time
- Mid-level
- 3 years
- Bachelor's degree
9d
TCSEPP Fatherhood Program Coordinator (West TN): Social Work Research and Public Service - UTK
University of Tennessee Health Science Center —Memphis, TN
- $50,000 a year
- Full-time
- Remote
- Customer service
- Mid-level
- Driver's License
Clinical Research Coordinator I
Iterative Health —Cordova, TN
- Full-time
- Mid-level
- Bachelor's degree
- Quality control
Quick Apply
Research Study Coordinator 2-Obstetrics and Gynecology
University of Tennessee Health Science Center —Memphis, TN
- $4,182.12 - $5,000.00 a month
- Weekends as needed
- Anatomy knowledge
- Management
- Mid-level
TCSEPP Fatherhood Program Coordinator (West TN): Social Work Research and Public Service - UTK
University of Tennessee - Knoxville —Memphis, TN
- $50,000 a year
- Full-time
- Remote
- Customer service
- Mid-level
- Driver's License
Research Project Coordinator-Preventive Medicine
University of Tennessee Health Science Center —Memphis, TN
- $4,182.12 - $4,583.33 a month
- Weekends as needed
- Mid-level
- Master's degree
- Bachelor's degree
Program Coordinator-Medicine
University of Tennessee Health Science Center —Memphis, TN
- $22.77 an hour
- Weekends as needed
- Primary Care
- Mid-level
- Analysis skills
Research Project Coordinator-Preventive Medicine
University of Tennessee - Knoxville —Memphis, TN
- $4,182.12 - $4,583.33 a month
- Weekends as needed
- Mid-level
- Master's degree
- Bachelor's degree
Program Coordinator-Medicine
University of Tennessee - Knoxville —Memphis, TN
- $22.77 an hour
- Weekends as needed
- Primary Care
- Mid-level
- Analysis skills
Research Study Coordinator-Psychiatry
University of Tennessee Health Science Center —Memphis, TN
- $21.69 an hour
- Full-time
- Psychiatry
- Driver's License
- Bachelor's degree
9d
Research Study Coordinator 2-Obstetrics and Gynecology
University of Tennessee - Knoxville —Memphis, TN
- $4,182.12 - $5,000.00 a month
- Weekends as needed
- Anatomy knowledge
- Management
- Mid-level
Clinical Research Coordinator II
Iterative Health —Southaven, MS
- Full-time
- Vital signs
- Mid-level
- 3 years
Quick Apply
Research Study Coordinator-Psychiatry
University of Tennessee - Knoxville —Memphis, TN
- $21.69 an hour
- Full-time
- Psychiatry
- Driver's License
- Bachelor's degree
9d

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Clinical Research Assistant
The Specialty Alliance —Germantown, TN
Knowledge of health care field; medical practice clinical and administrative systems, departments, and practices, including clinical financial policies and…
$27 - $29 an hour
Quick Apply
Administrative Associate 2-Nursing Research Programs
University of Tennessee Health Science Center —Memphis, TN
JOB SUMMARY/ESSENTIAL JOB FUNCTIONS: The Administrative Associate 2 supports the successful implementation of a one-year, part-time project focused on cancer…
$18.54 an hour

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Clinical Research Coordinator I
Nationwide Children's Hospital —Columbus, OH
Recruits, consents and enrolls subjects according to ICH/GCP regulations, and subjects’ rights through institutional IRB, federal and state regulations; answers…
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Nationwide Children's Hospital —Columbus, OH
Recruits, consents and enrolls subjects according to ICH/GCP regulations, and subjects’ rights through institutional IRB, federal and state regulations; answers…

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Clinical Research Coordinator

The Specialty Alliance -
Germantown, TN

Quick Apply

Job Details

Full-time
$50,000 - $75,000 a year

Qualifications

Managing scientific research projects
Computer operation
Management
Phone communication
Practice management software
Patient management software
Implementing research protocols
Telephone systems
Multi-line phone systems
Patient interaction
Clinical quality assurance standards
Training
Clinical trial support in drug product development
Medical terminology

Full Job Description

POSITION SUMMARY: Experienced Research Coordinator that builds and leads a newly growing research department. Will have the opportunity to help create a premier research facility. Will be provided with the necessary support, budget, staff, etc. This position works closely with PI and Sub-Is on the various studies. Will be working in highly motivated large private practice urology group.

JOB RELATIONSHIPS:

Reports to the Clinical Research Director, Vice President of Research, Market President, and the physicians at the local Market Clinic
Collaborates with experienced patient navigators, IT, and data management.

ROLE QUALIFICATIONS: (experience, education, and skills)

Able to handle a high volume of coordinating work, including managing multiple studies at a time of varying indications.
Acts as an experienced resource for Clinical Research Coordinators I and Research Assistants during new hire training, newly initiated trials, and trial transitions

. • Demonstrate the ability to successfully oversee complex trials.

• Demonstrate the ability to understand and navigate Urology Austin and the various roles of stakeholders to ensure continuity of patient care. • Must have knowledge of and experience with relevant federal and state regulatory guidelines.

Must have > 2 yrs previous experience conducting clinical trials.
Urology based clinical experience preferred. Willingness to perform urology required procedures to conduct urology research.
Experience with evaluating and implementing study protocols.
Certification via ACRP or the equivalent preferred.
Proficiency in computer software use, including Microsoft Office, EMR and Practice Management systems.
Effective time management and the ability to prioritize work.
Excellent communication skills and the ability to interact with all levels of management, staff, and physicians.

ESSENTIAL JOB RESPONSIBLITIES:

Leads the recruitment of studies, protocol conduction, and communication with study sponsors.
Maintain certifications in, and continually update knowledge of, FDA, GCP, ICH, federal and state regulations, etc.
Obtain and maintain consent of patients with the highest ethical standards.
Work directly with patients to conduct all study visits. Ex: screen, consent, take medical history, complete necessary procedures including EKG, blood draw, vitals, etc.

Communicate with and support patients end to end during trial participation and their families as necessary. • Work with the EMR and data management systems to complete all data and source requirements for visits.

Must have or gain knowledge of relevant software/programs, including the CTMS.
Have a basic and working knowledge of trial design, statistical methods, etc.
Triage, record, and report adverse events. Record and report any protocol deviations.
Work closely with IRB and study sponsors, PIs and Sub-Is. Attend necessary meetings and calls.

• Directly work with the Regional Manager and Research Director to assist overseeing all daily operations and implementation of policies and procedures in the department. • Maintain HIPAA compliant communication and confidentiality, at all times.

Participate in site visits, SIVs, monitoring, etc.
Complete necessary study close-out steps and documentation.
Conduct blood draws and laboratory procedures as required per study.

• Manage IP accountability and perform drug dosing and instillations per study requirements. • Assist with other duties assigned. PERFORMANCE

REQUIREMENTS: Knowledge

Knowledge of health care field; medical practice clinical and administrative systems, departments, and practices.
Understanding of medical terminology. Skills
Ability to use multi-line phone systems and basic computer systems.
Interpersonal and communication both with internal staff and external customers. Clinical Research Coordinator II Updated 11.2025 Abilities
Skill in reading medical chart terminology.

. • Phlebotomy.

Ability to communicate effectively with patients, staff, and external contacts via phone, in person, and through electronic mail.
Elicit appropriate information for patients to clinic staff.
Ability to read and understand information and ideas presented in writing.
Ability to apply general rules to specific problems to produce answers that make sense – deductive reasoning

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Refine Your Search

research coordinator jobs in memphis tn

Clinical Research Coordinator

Program Coordinator - Cancer Predisposition

TCSEPP Fatherhood Program Coordinator (West TN): Social Work Research and Public Service - UTK

Clinical Research Coordinator I

Research Study Coordinator 2-Obstetrics and Gynecology

TCSEPP Fatherhood Program Coordinator (West TN): Social Work Research and Public Service - UTK

Research Project Coordinator-Preventive Medicine

Program Coordinator-Medicine

Research Project Coordinator-Preventive Medicine

Program Coordinator-Medicine

Research Study Coordinator-Psychiatry

Research Study Coordinator 2-Obstetrics and Gynecology

Clinical Research Coordinator II

Research Study Coordinator-Psychiatry

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