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Computer Vision Research Assistant Jobs in Memphis, TN

Care Access

Clinical Research Coordinator II

Memphis, TN

$23.50 - $31.25/hr

Patient Recruitment * Assist with planning and creation of appropriate recruitment materials ... Strong computer skills with demonstrated abilities using clinical trials database, IVR systems ...

Care Access

Clinical Research Coordinator II

Memphis, TN

$23.50 - $31.25/hr

Patient Recruitment * Assist with planning and creation of appropriate recruitment materials.  ... Strong computer skills with demonstrated abilities using clinical trials database, IVR systems ...

Care Access

Clinical Research Coordinator II

Memphis, TN · On-site

$23.50 - $31.25/hr

Patient Recruitment * Assist with planning and creation of appropriate recruitment materials ... Strong computer skills with demonstrated abilities using clinical trials database, IVR systems ...

Porter-Leath

Administrative Assistant

Memphis, TN · On-site

$15.35 - $18.58/hr

Clerical duties to include typing of letters, memos and reports using a computer; preparation and ... Skill to evaluate given information, research additional information needed, and evaluate and ...

Porter-Leath

Administrative Assistant

Memphis, TN

$15.35 - $18.58/hr

Clerical duties to include typing of letters, memos and reports using a computer; preparation and ... Skill to evaluate given information, research additional information needed, and evaluate and ...

Porter-Leath

Administrative Assistant

Memphis, TN · On-site

$15.35 - $18.58/hr

Clerical duties to include typing of letters, memos and reports using a computer; preparation and ... Skill to evaluate given information, research additional information needed, and evaluate and ...

Accura Engineering

SUE CAD Technician

Memphis, TN · On-site

... * Assist in other related tasks as needed to support project goals and client needs. Education ... Comprehensive health, dental, and vision insurance. * Retirement savings plan with company match.

AutoZone

UX User Experience Research Manager

Memphis, TN · On-site

$113K/yr

... computer science, human-computer interaction (HCI), related field or four years equivalent ... Medical, dental and vision plans * Exclusive discounts and perks, including an AutoZone in-store ...

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All JobsComputer Vision Research JobsComputer Vision Research Assistant JobsComputer Vision Research Assistant Jobs in Memphis, TN

Computer Vision Research Assistant information

See Memphis, TN salary details

$32.5K

$46.9K

$61.7K

How much do computer vision research assistant jobs pay per year?

As of Aug 8, 2026, the average yearly pay for computer vision research assistant in Memphis, TN is $46,920.00, according to ZipRecruiter salary data. Most workers in this role earn between $36,900.00 and $53,900.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a computer vision research assistant?

To thrive as a Computer Vision Research Assistant, you need a strong background in computer science, mathematics, and image processing, often supported by a relevant degree or coursework. Experience with machine learning frameworks (such as TensorFlow or PyTorch), programming languages like Python or C++, and familiarity with computer vision libraries (like OpenCV) are typically required. Critical thinking, problem-solving abilities, and effective communication help distinguish top candidates in collaborative research environments. These skills and qualifications are essential for developing innovative solutions, efficiently analyzing visual data, and contributing to cutting-edge research projects.

What is a computer vision research assistant?

Computer Vision Research Assistants are professionals who support research projects focused on developing algorithms and systems that enable computers to interpret and process visual information from the world, such as images and videos. They assist with tasks like data collection, annotation, running experiments, literature review, and implementing computer vision models. These roles often require knowledge of programming, machine learning, and image processing techniques, and are commonly found in academic labs, tech companies, and research institutions. Their work helps advance the field by contributing to innovations in areas like object recognition, autonomous vehicles, medical imaging, and augmented reality.

What does a computer vision research assistant do?

As a Computer Vision Research Assistant, you can expect to work on tasks such as collecting and annotating image datasets, implementing and testing computer vision algorithms, and assisting with experimental design for research studies. You will frequently collaborate with graduate students, faculty, or senior researchers to analyze data and prepare reports or presentations. Your daily work may involve coding in Python or MATLAB, running experiments, and troubleshooting model performance, all within a collaborative research team environment.
What are the most commonly searched types of Computer Vision Research jobs in Memphis, TN? The most popular types of Computer Vision Research jobs in Memphis, TN are:
What are popular job titles related to Computer Vision Research Assistant jobs in Memphis, TN? For Computer Vision Research Assistant jobs in Memphis, TN, the most frequently searched job titles are:
What job categories do people searching Computer Vision Research Assistant jobs in Memphis, TN look for? The top searched job categories for Computer Vision Research Assistant jobs in Memphis, TN are:
Computer Vision Research Assistant jobs near you
Infographic showing various Computer Vision Research Assistant job openings in Memphis, TN as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 16% Part Time, and 5% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $46,920 per year, or $22.6 per hour.

Clinical Research Coordinator II

Care Access

Memphis, TN

$23.50 - $31.25/hr

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 28 days ago

Job description

How This Role Makes a Difference

The Clinical Research Coordinator's primary responsibilities are to utilize Good Clinical Practices (GCP)s in the process of screening, enrolling and closely monitoring clinical research study subjects while ensuring protocol and regulatory compliance. 

How You'll Make An Impact
  • Patient Coordination 
    • Prioritize activities with specific regard to protocol timelines 
    • Maintain adherence to FDA regulations and ICH guidelines in all aspects of conducting clinical trials. 
    • Maintain effective relationships with study participants and other care Access Research personnel. 
    • Balances protocol needs with patient experience; proactively addresses concerns. 
    • Monitors quality metrics; prevents deviations; resolves queries quickly. 
    • Interact in a positive, professional manner with patients, .representatives, investigators and Care Access Research personnel and management. 
    • Coordinate and attend pre-study site visits, site initiation visits, and monitor visits with clinical staff and Sponsor/CRO representatives. 
    • Mentors CRC I peers; provides onboarding and daytoday guidance. 
    • Identify adverse events (AEs) and Serious Adverse Events (SAEs) and promptly notify Principal Investigator and Sponsor (where appropriate) 
    • Moderate complexity; mixed visit types, active IP and AE/SAE workflows. 
    • Can operate as solo CRC onsite. 
    • Prescreen study candidates 
    • Obtain informed consent per Care Access Research SOP . 
    • Complete visit procedures in accordance with protocol. 
    • Complete basic clinical procedures, such as blood draws, vital signs, ECGs, etc. 
    • Review laboratory results, ECGs, and other test results (e.g., MRIs) for completeness and alert values, ensuring investigator review in a timely fashion. 
    • Discuss study medication, required procedures, eligibility criteria and impact on office flow with Investigator and site staff. 
  • Documentation 
    • Record data legibly and enter in real time on paper or e-source documents 
    • Accurately record study medication inventory, medication dispensation, and patient compliance. 
    • Resolve data management queries and correct source data within sponsor provided timelines 
    • Assist regulatory personnel with completion and filing of regulatory documents. 
    • Assist in the creation and review of source documents. 
  • Patient Recruitment 
    • Assist with planning and creation of appropriate recruitment materials. 
    • Assist in development of recruitment plan and obtain listing of potential candidates to contact from subject database. 
    • Actively work with recruitment team in calling and recruiting subjects 
  • Review and assess protocol (including amendments) for clarity, logistical feasibility 
  • Ensure that all training and study requirements are met prior to trial conduct. 
  • Communicate clearly verbally and in writing. 
  • Anticipates needs; proposes solutions; manages change effectively. 
  • Attend Investigator meetings as required. 
  • Owns studies; prioritizes competing demands; mentors CRC I. 
  • Ensure adequate supplies have arrived on site for protocol initiation (lab kits, study medication, specialized equipment, IVRS/EDC access and passwords) 
The Expertise Required
  • Ability to understand and follow institutional SOPs. 
  • Excellent working knowledge of medical and research terminology 
  • Excellent working knowledge of federal regulations, good clinical practices (GCP) 
  • Operates independently for most study activities; escalates complex issues as needed. 
  • Ability to communicate and work effectively with a diverse team of professionals. 
  • Strong organizational, prioritization and leadership skills and capabilities with a strong attention to detail 
  • Strong computer skills with demonstrated abilities using clinical trials database, IVR systems, electronic data capture, MS word and excel. 
  • Critical thinker and problem solver 
  • Friendly, outgoing personality; maintain a positive attitude under pressure. 
  • High level of self-motivation and energy 
  • Excellent professional writing and communication skills 
  • Manages stakeholder communications; facilitates visits and meetings. 
  • Ability to work independently in a fast-paced environment with minimal supervision. 
Certifications/Licenses, Education, and Experience:
  • Minimum Education:
    • Bachelor's Degree preferred, or equivalent combination of education, training and experience. 
  • Minimum Experience:
    • 3 years prior Clinical Research Coordinator experience required 
    • Prefer 1 year of experience as a Care Access Research Clinical Research Coordinator    
    • Recent phlebotomy experience required
How We Work Together
  • Location: This is an on-site position with regional commute requirements
    • Travel: This role requires up to 10% travel requirements further explained below. Length of travel will depend upon study requirements, staff needs, and company initiatives. 
      • Type of travel required: Regional (within 100 miles) 
    • Physical demands associated with this position Include: The ability to use keyboards and other computer equipment.
      • Walking, Standing, Sitting, Lifting (up to 25lbs and overhead), Driving - 20%

The expected pay range for this role is $60,000 - $90,000 USD per year for full time team members.

Benefits & Perks (US Full Time Employees)
  • Paid Time Off (PTO) and Company Paid Holidays
  • 100% Employer paid medical, dental, and vision insurance plan options
  • Health Savings Account and Flexible Spending Accounts
  • Bi-weekly HSA employer contribution
  • Company paid Short-Term Disability and Long-Term Disability
  • 401(k) Retirement Plan, with Company Match 
  • Relocation Support Provided  

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