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Clinical Research Lab Jobs (NOW HIRING)

$23.50 - $31.25/hr

The Clinical Research Coordinator under the direction of the Site Manager/Director and the ... May perform basic lab procedures per protocol, such as: blood specimen collection, centrifuge ...

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Clinical Research Lab information

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$49K

$107.3K

$189K

How much do clinical research lab jobs pay per year?

As of Jun 19, 2026, the average yearly pay for clinical research lab in the United States is $107,336.00, according to ZipRecruiter salary data. Most workers in this role earn between $81,000.00 and $122,500.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in a Clinical Research Lab, and why are they important?

To thrive in a Clinical Research Lab, you need a solid background in biological sciences or related fields, experience with laboratory techniques, and often at least a bachelor’s degree in science. Familiarity with laboratory information management systems (LIMS), data analysis software, and regulatory compliance certifications such as Good Clinical Practice (GCP) is typically required. Strong attention to detail, effective teamwork, and clear communication skills are essential soft skills in this environment. These competencies ensure accurate data collection, regulatory adherence, and successful collaboration on research projects.

What is the highest paying clinical research job?

In clinical research, senior roles such as Clinical Research Director or Principal Investigator tend to have the highest salaries, often exceeding six figures annually. These positions typically require extensive experience, advanced degrees, and leadership skills, and may involve overseeing multiple studies or teams.

What qualifications are needed for clinical research?

Clinical research professionals typically need a bachelor's degree in a health-related field such as biology, nursing, or pharmacy. Relevant skills include attention to detail, good communication, and knowledge of Good Clinical Practice (GCP) guidelines. Some roles may require certification, such as the Certified Clinical Research Professional (CCRP).

What is a clinical research lab?

A clinical research lab is a specialized facility where scientific studies involving human participants are conducted to evaluate the safety and effectiveness of medications, medical devices, diagnostics, or treatment protocols. These labs play a crucial role in advancing medical knowledge by generating data that supports regulatory approvals and clinical practice guidelines. The work in such labs is highly regulated to ensure the integrity of the research and the safety of participants. Clinical research labs often collaborate with hospitals, universities, and pharmaceutical companies to conduct these studies.

Can you be a CRA with no experience?

Entering a Clinical Research Associate (CRA) role typically requires some background in clinical trials, healthcare, or related fields, but entry-level positions may be available for candidates with strong organizational skills and relevant certifications such as GCP training. Most employers prefer candidates with some related experience or education, but training programs and internships can provide a pathway for those without prior CRA experience.

Which is better, CRC or CRA?

A Clinical Research Coordinator (CRC) manages daily clinical trial activities at research sites, while a Clinical Research Associate (CRA) monitors trials remotely or on-site to ensure compliance and data quality. Both roles require knowledge of Good Clinical Practice (GCP) and may involve different certifications; the choice depends on whether you prefer site management or trial oversight.

What is the difference between Clinical Research Lab vs Clinical Research Coordinator?

AspectClinical Research LabClinical Research Coordinator
CredentialsTypically requires laboratory science degrees or certificationsRequires clinical research certifications and healthcare-related degrees
Work EnvironmentLaboratories, research facilitiesClinics, hospitals, research sites
Employer & IndustryResearch institutions, biotech companiesHospitals, clinical trial sites
Job FocusLaboratory testing, sample analysisParticipant management, study coordination

While both roles are essential in clinical research, a Clinical Research Lab focuses on laboratory testing and analysis, whereas a Clinical Research Coordinator manages participant recruitment and study logistics. Understanding these differences helps in choosing the right career path or job search focus.

What are some common challenges faced by professionals working in a clinical research lab, and how can they be addressed?

Professionals in a clinical research lab often encounter challenges such as strict regulatory requirements, tight project timelines, and the need for meticulous attention to detail. Maintaining accurate documentation and adhering to protocols is crucial, which can be demanding under pressure. Effective communication within multidisciplinary teams—such as clinicians, data managers, and laboratory technicians—is essential for smooth workflow. Proactively seeking mentorship, staying updated on regulatory changes, and participating in team meetings can help mitigate these challenges and foster a collaborative environment.
More about Clinical Research Lab jobs
What cities are hiring for Clinical Research Lab jobs? Cities with the most Clinical Research Lab job openings:
What states have the most Clinical Research Lab jobs? States with the most job openings for Clinical Research Lab jobs include:
Infographic showing various Clinical Research Lab job openings in the United States as of June 2026, with employment types broken down into 6% As Needed, 83% Full Time, 5% Part Time, and 6% Contract. Highlights an 89% Physical, 3% Hybrid, and 8% Remote job distribution, with an average salary of $107,336 per year, or $51.6 per hour.
Research Lab Assistant

Research Lab Assistant

Tennessee Oncology

Nashville, TN • On-site

Full-time

Posted 10 days ago


Tennessee Oncology rating

6.4

Company rating: 6.4 out of 10

Based on 26 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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