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Cra Clinical Research Associate Jobs in Normal, AL

OneOncology LLC

EHR Systems Specialist

Huntsville, AL · On-site

... research and involvement in Phase I-IV clinical trials gives our patients the opportunity to ... High school diploma or equivalent required;associate's or bachelor'sdegree in health information ...

OneOncology LLC

Infusion RN

Huntsville, AL · On-site

... research and involvement in Phase I-IV clinical trials gives our patients the opportunity to ... Must have an Associate's degree in Nursing, Bachelor's preferred. * Must have at least (1) year ...

New

OneOncology LLC

Coder

Huntsville, AL · On-site

$18.50 - $24.75/hr

... research and involvement in Phase I-IV clinical trials gives our patients the opportunity to ... Must have an Associate's degree in Medical Coding or a certification from accredited school in ...

OneOncology LLC

Certified Professional Coder

Huntsville, AL · On-site

$22.50 - $29.75/hr

... research and involvement in Phase I-IV clinical trials gives our patients the opportunity to ... Must have an Associate's degree in Medical Coding or a certification from accredited school in ...

OneOncology LLC

Certified Professional Coder

Huntsville, AL · On-site

$22.50 - $29.75/hr

... research and involvement in Phase I-IV clinical trials gives our patients the opportunity to ... Must have an Associate's degree in Medical Coding or a certification from accredited school in ...

OneOncology LLC

Certified Professional Coder

Huntsville, AL · On-site

$22.50 - $29.75/hr

... research and involvement in Phase I-IV clinical trials gives our patients the opportunity to ... Must have an Associate's degree in Medical Coding or a certification from accredited school in ...

OneOncology LLC

Coder

Huntsville, AL · On-site

$18.50 - $24.75/hr

... research and involvement in Phase I-IV clinical trials gives our patients the opportunity to ... Must have an Associate's degree in Medical Coding or a certification from accredited school in ...

OneOncology LLC

Certified Professional Coder

Huntsville, AL · On-site

$22.50 - $29.75/hr

... research and involvement in Phase I-IV clinical trials gives our patients the opportunity to ... Must have an Associate's degree in Medical Coding or a certification from accredited school in ...

OneOncology LLC

PRN CT Technologist

Huntsville, AL · On-site

... research and involvement in Phase I-IV clinical trials gives our patients the opportunity to ... Must have Associate's Degree in Medical Technology or related field. * Must be certified by the ...

OneOncology LLC

PRN CT Technologist

Huntsville, AL · On-site

... research and involvement in Phase I-IV clinical trials gives our patients the opportunity to ... Must have Associate's Degree in Medical Technology or related field. * Must be certified by the ...

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Showing results 21-40

All JobsCra Clinical Research Associate JobsCra Clinical Research Associate Jobs in Normal, AL

Cra Clinical Research Associate information

See Normal, AL salary details

$10

$36

$61

How much do cra clinical research associate jobs pay per hour?

As of Sep 6, 2026, the average hourly pay for cra clinical research associate in Normal, AL is $36.50, according to ZipRecruiter salary data. Most workers in this role earn between $25.58 and $46.73 per hour, depending on experience, location, and employer.

What is a clinical research associate?

CRA Clinical Research Associates are professionals who monitor clinical trials to ensure they are conducted in accordance with regulatory requirements, study protocols, and Good Clinical Practice guidelines. They act as a bridge between the sponsor of a clinical trial and the sites where the trial is conducted, overseeing data collection, patient safety, and compliance. Their responsibilities include site visits, reviewing documentation, and ensuring accurate reporting of study results. CRAs play a critical role in advancing medical research by maintaining the integrity and quality of clinical studies.

What are the key skills and qualifications needed to thrive as a clinical research associate?

To thrive as a Clinical Research Associate (CRA), you need a solid background in life sciences, experience in clinical trial monitoring, and typically a bachelor's degree in a related field. Familiarity with Good Clinical Practice (GCP) guidelines, electronic data capture (EDC) systems, and regulatory requirements is essential, and certifications like ACRP or SOCRA are often advantageous. Strong attention to detail, organizational skills, effective communication, and adaptability help CRAs excel in coordinating studies and collaborating with diverse stakeholders. These skills ensure clinical trials are conducted ethically, efficiently, and in compliance with regulatory standards, safeguarding both data integrity and patient safety.

What are some common challenges faced by clinical research associates when managing multiple clinical trial sites?

CRAs often juggle oversight of multiple clinical trial sites, which can present challenges such as coordinating visits, ensuring consistent protocol adherence, and managing varying site performance. Effective communication and strong organizational skills are crucial, as CRAs need to address site-specific issues, maintain accurate documentation, and ensure timely data collection. Additionally, adapting to diverse team dynamics and staying updated with regulatory requirements across sites are common aspects of the role. Employers typically provide training and support, but successful CRAs proactively develop strategies to manage these complexities.

What is the difference between Cra Clinical Research Associate vs Clinical Trial Coordinator?

AspectCra Clinical Research AssociateClinical Trial Coordinator
CredentialsTypically requires a bachelor's degree in life sciences, nursing, or related field; certifications like CCRP or RAC are commonUsually holds a bachelor's degree in health sciences, nursing, or related field; certifications like CCRP are also beneficial
Work EnvironmentWorks primarily on-site at clinical trial sites, monitoring study progress and complianceCoordinates trial activities, manages schedules, and ensures protocol adherence, often working at trial sites or offices
Employer & IndustryEmployed by pharmaceutical companies, CROs, or research institutions in the clinical research industryEmployed by hospitals, research centers, or pharmaceutical companies to manage trial logistics

While both roles support clinical trials, Cra Clinical Research Associates focus on monitoring and compliance, whereas Clinical Trial Coordinators handle trial logistics and coordination. Both require relevant certifications and work in similar environments within the clinical research industry.

What cities near Normal, AL are hiring for Cra Clinical Research Associate jobs?

Cities near Normal, AL with the most Cra Clinical Research Associate job openings:

Cra Clinical Research Associate jobs near you
Infographic showing various Cra Clinical Research Associate job openings in Normal, AL as of August 2026, with employment types broken down into 3% As Needed, 74% Full Time, 15% Part Time, and 8% Contract. Highlights an 85% Physical, 1% Hybrid, and 14% Remote job distribution, with an average salary of $75,910 per year, or $36.5 per hour.

Medical Laboratory Technician - Float

OneOncology LLC

Huntsville, AL • On-site

Full-time

Re-posted 6 days ago

OneOncology rating

7.9

Company rating: 7.9 out of 10

Based on 18 frontline employees who took The Breakroom Quiz

Job description

Clearview Cancer Institute is north Alabama's leading cancer treatment facility. For over 30 years Clearview Cancer Institute has provided leading-edge treatment and compassionate care to those diagnosed with cancer or blood disorders. Clearview offers every service and amenity needed in an outpatient setting and our dedication to research and involvement in Phase I-IV clinical trials gives our patients the opportunity to receive potentially life-saving treatment options.
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:
Job Purpose
The Medical Laboratory Technician performs moderate and high complexity laboratory procedures to provide clinical information for diagnosis, treatment, and prevention of disease.
Essential Job Functions
Technical:
  • Successfully perform all phases of laboratory testing: pre-analytic, analytic and post-analytics processes
  • Perform specimen processing including verifying proper sample labeling and specimen collection requirements.
  • Know specimen acceptability and rejection criteria for testing and troubleshoot problems relating to specimen analysis.
  • Evaluate results in LIS system and perform delta checks.
  • Process and distribute lab reports to appropriate individuals and institutions.
  • Receive and inventory supplies and reagents according to lab protocol.
  • Detect, troubleshoot, and correct instrument reagent and system failures, perform calibrations and preventative maintenance on equipment.

QA/QC/Regulatory:
  • Report lab results within established turnaround times
  • Document critical values and corrected results in the LIS and notify physician staff.
  • Follow Westgard rules, and recognize shifts/trends occurring on Levy-Jennings charts.
  • Document out of range quality control values and take corrective action.
  • Participate in continuous improvement activities, examine existing processes/procedures, and look for ways to improve them.
  • Complete necessary documentation when specimen variance or adverse events occur
  • Perform competency testing as required.
  • Adhere to all regulatory standards within the clinical laboratory.

Safety/Organizational/Productivity:
  • Follow institution's safety procedures.
  • Follow Universal Precautions, wear PPE.
  • Acts independently and accepts responsibility of the clinical laboratory's policy and procedures.
  • Oversee performance of Laboratory Assistants as needed.
  • Complete 12 hours of continuing education annually.

Communication/Teamwork:
  • Maintain positive working relationship with fellow staff and clinic personnel.
  • Must be able to interact well with patients, employees, physicians and management.
  • Answer questions from patients, physicians, and nursing staff regarding clinical laboratory.

Qualifications
  • Must have excellent organizational skills, be able to prioritize and manage tasks in a timely and effective manner
  • Must have excellent communication skills, both oral and written
  • Willing to adapt to a flexible schedule and work environment

Education
  • Associate's Degree in Laboratory Science with MLT certification from a recognized credentialing agency.
  • Must have (2) years' experience in a clinical laboratory setting.
  • Must have basic computer skills.

Working Conditions
This position works in the clinical laboratory of a busy outpatient oncology/hematology clinic. This person will be required to work closely with coworkers and management. This position requires that the employee handle bodily fluids and chemicals daily.
Physical Requirements
This position requires that the employee be able to stand and walk for long periods of time, up to eight hours a day. This position also requires that the employee be able to perform mild physical labor to complete the tasks at hand.
Direct reports
This position is not a supervisory position.

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