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Entry Level Clinical Research Associate Jobs in Cleveland, TN

In partnership with our Medtech client, we are building a team of Associate Territory Manager ... clinical research services, commercial insights and healthcare intelligence to the life sciences ...

In partnership with our Medtech client, we are building a team of Associate Territory Manager ... clinical research services, commercial insights and healthcare intelligence to the life sciences ...

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... entry-level professional staff. * Ensure high levels of customer and client satisfaction by ... Promote best practices by staying current with nutrition research, trends, policies, and ...

... entry-level professional staff. * Ensure high levels of customer and client satisfaction by ... Promote best practices by staying current with nutrition research, trends, policies, and ...

... entry-level professional staff. * Ensure high levels of customer and client satisfaction by ... Promote best practices by staying current with nutrition research, trends, policies, and ...

... entry-level professional staff. * Ensure high levels of customer and client satisfaction by ... Promote best practices by staying current with nutrition research, trends, policies, and ...

... entry-level professional staff. * Ensure high levels of customer and client satisfaction by ... Promote best practices by staying current with nutrition research, trends, policies, and ...

Research information in catalogs, specifications, corporate standards, or other reference material ... Associates degree in Drafting & Design or equivalent certification is preferred. * Experience in ...

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Entry Level Clinical Research Associate information

What is an entry level clinical research associate?

An Entry Level Clinical Research Associate (CRA) is responsible for monitoring clinical trials to ensure compliance with regulatory requirements, ethical guidelines, and study protocols. They assist in site selection, data collection, and verifying that study procedures are properly followed. Entry-level CRAs typically work under the supervision of senior CRAs and may travel to different clinical sites. Strong attention to detail, knowledge of Good Clinical Practice (GCP) guidelines, and organizational skills are essential. This role is a starting point for a career in clinical research, with opportunities for growth into senior CRA or project management positions.

What are the typical daily responsibilities of an entry level clinical research associate?

As an Entry Level Clinical Research Associate, your day-to-day work generally involves assisting with monitoring clinical trial sites, reviewing study documentation, and ensuring adherence to protocol and regulatory requirements. You may support more senior team members in conducting on-site or remote visits, tracking patient recruitment, and managing data collection. Additionally, you’ll communicate regularly with site staff and other stakeholders to resolve issues and ensure data quality. This hands-on experience is essential for building expertise in clinical research processes and advancing toward more senior CRA roles.

What are the key skills and qualifications needed to thrive as an entry level clinical research associate?

To thrive as an Entry Level Clinical Research Associate, you typically need a bachelor's degree in life sciences or a related field, a solid understanding of clinical trial protocols, and attention to detail. Familiarity with Good Clinical Practice (GCP) guidelines, electronic data capture (EDC) systems, and regulatory documentation is often required. Strong communication, organization, and problem-solving abilities help you effectively collaborate with study sites and team members. These skills are critical to ensure the accuracy, compliance, and successful progression of clinical studies.

What job categories do people searching Entry Level Clinical Research Associate jobs in Cleveland, TN look for?

The top searched job categories for Entry Level Clinical Research Associate jobs in Cleveland, TN are:

What cities near Cleveland, TN are hiring for Entry Level Clinical Research Associate jobs?

Cities near Cleveland, TN with the most Entry Level Clinical Research Associate job openings:

Infographic showing various Entry Level Clinical Research Associate job openings in Cleveland, TN as of August 2026, with employment types broken down into 2% As Needed, 73% Full Time, 18% Part Time, and 7% Contract. Highlights an 84% Physical, 1% Hybrid, and 15% Remote job distribution.

Research Lab Assistant

Tennessee Oncology

Chattanooga, TN • On-site

Full-time

Re-posted 12 days ago


Key responsibilities

  • Collect and process human biological specimens such as blood, urine, and tissue following established protocols.

  • Maintain accurate records of samples, manage specimen storage and shipment, and document clinical data in compliance with protocols.

  • Assist with laboratory operations including specimen labeling, sorting, inventory management, equipment maintenance, and ensuring a safe and sterile environment.


Tennessee Oncology rating

6.8

Company rating: 6.8 out of 10

Based on 27 frontline employees who took The Breakroom Quiz


Job description

Tennessee Oncology, one of the nation's largest, community-based cancer care specialists, is home to one of the leading clinical trial networks in the country. Established 1976 in Nashville, Tennessee Oncology's mission remains unchanged: To provide access to high-quality cancer care and the expertise of clinical research for all patients, at convenient locations within their community and close to their home. Our growing network of physicians and locations is based on this mission. Tennessee Oncology is committed to advancing both the science of detection and targeted treatments, and to making these advances available to every patient. We believe caring for cancer patients is a privilege.
Why Join Us? We are looking for talented and highly-motivated individuals who demonstrate a natural desire to support the meaningful work of community oncologists and the patients we serve.
Job Description:
This position will play an essential role in biological specimen collection, processing, storage, and shipment for clinical research studies conducted at Tennessee Oncology clinics.
ESSENTIAL FUNCTIONS:
  • Collecting & Processing Human Biological Specimens
    • May perform phlebotomy and other biological specimen collection and point of care testing, as needed, following established procedures and protocols, ensuring study participant comfort and safety
    • May serve as an assistant to investigator during dissections or surgery. Provides research support of tissue collection, processing and specimen distribution for research studies and clinical trials in outpatient clinics.
    • Maintain knowledge of specimen collection devices and tubes.
    • Maintains laboratory and surgical areas with proper aseptic techniques.
    • Label, receive and process samples (blood, urine, tissue etc.) for clinical trials per specific protocol guidelines to include logging samples into and out of the department.
    • Will require travel to location where specimen is being collected to obtain specimens from various sites in. Travel mileage to be reimbursed with properly filled out expense form.
  • Data and Outside Specimen Management
    • Request, receive and return tissue samples from outside pathology facilities.
    • Send tissue blocks to vendor to have slides cut and ship slides to the appropriate study's lab
    • Document study participant information and clinical data following stringent data management protocols, while maintaining patient confidentiality
    • Maintain clear and accurate records, both written and electronic, of laboratory data. Data must be readily accessible by Research Laboratory Manager
  • Laboratory Operations:
    • Organizes work by matching protocol requirements with lab kit supply/inventory management, specimen collection; labeling; sorting specimens; logging specimens; storage, shipment, and tracking as required
    • Maintain accurate records of all collected samples, ensuring their correct labeling and secure storage
    • Collaborate with the multidisciplinary team, including researchers, clinicians, and pathologists, to ensure efficient operations and high-quality research output
    • Receives and directs specimens for send-out testing.
    • Helps with administrative duties including, completing proficiency testing, Quality control checks, etc. as needed.
    • Monitors laboratory temperatures including ambient room, refrigerator and freezer temperatures and troubleshoots appropriate deviations.
    • Follow strict safety protocols, maintaining a clean and safe environment in the lab and during sample collection and processing
    • Practice safe work practices by using PPE appropriately.
    • Maintain equipment, keep lab and ancillary clinics stocked with adequate research lab manuals, kits, and supplies
    • Prepare and perform paperwork and clerical duties as necessary including answering phones, computer entry, etc.
    • Assist clinical research teams, study sponsors, and central/local laboratories with data collection, sample tracking, and query resolution
  • Other duties as may be assigned.

KNOWLEDGE, SKILLS & ABILITIES:
  • Ability to make independent decisions, process information accurately, manage multiple projects simultaneously and be organized.
  • Ability to accurately pipette and maintain sterile conditions as required.
  • Effective oral and written communication skills and excellent interpersonal skills required.
  • Strong computer skills especially with Excel and Word spreadsheets.

EDUCATION & EXPERIENCE:
  • High School Diploma or Equivalent
  • Valid Driver's License required
  • Training and/or certification as a Laboratory Technician, Lab Technician, Phlebotomist, or Medical Assistant per state/local requirements 1 year experience in the medical field
  • Minimum of 2 year experience in a clinic, medical or laboratory setting.
  • Associate degree or higher preferred
  • Clinical research or oncology experience is highly preferred.

PHYSICIAL REQUIREMENTS:
  • Must be willing and able to lift up to 25 pounds.
  • Must be willing and able to travel to satellite clinics & biopsy facilities when necessary.

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