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Cra Clinical Research Associate Jobs in Normal, AL

... research and involvement in Phase I-IV clinical trials gives our patients the opportunity to ... Must hold an Associate's degree in Nursing, Bachelor's preferred. * Must hold an Alabama RN license.

... research and involvement in Phase I-IV clinical trials gives our patients the opportunity to ... Must hold an Associate's degree in Nursing, Bachelor's preferred. * Must hold an Alabama RN license.

... research and involvement in Phase I-IV clinical trials gives our patients the opportunity to ... Must hold an Associate's degree in Nursing, Bachelor's preferred. * Must hold an Alabama RN license.

... research and involvement in Phase I-IV clinical trials gives our patients the opportunity to ... Must hold an Associate's degree in Nursing, Bachelor's preferred. * Must hold an Alabama RN license.

Showing results 41-49

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:

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.

Full-time

Re-posted 13 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 Business Office Generalist will support the daily administrative and financial operations Oncology Specialties, PC. This role is responsible for a wide range of front-end and back-end office functions, including insurance verification, billing support, and customer service.

Essential Job Functions

  • Perform demographic updates and insurance verification.
  • Obtain referrals as required.
  • Collect copayments, deductibles, and outstanding balances in accordance with practice policies.
  • Assist with charge entry, claim submission, and payment posting.
  • Communicate with insurance companies regarding claim status, eligibility, and coverage issues.
  • Respond to patient inquiries related to billing, insurance, and account balances.
  • Maintain accurate and up-to-date patient and financial records in the practice management system.
  • Perform other administrative duties as assigned.

Qualifications

  • Must have knowledge of medical terminology, insurance plans, and billing procedures.
  • Must be able to prioritize and manage time efficiently.
  • Must have strong problem-solving and critical thinking skills.
  • Must be able to collaborate effectively across multiple departments.
  • Must have strong organizational skills and attention to detail.
  • Must have excellent communication and customer service skills.
  • Must have a demonstrated commitment to accuracy and accountability in all aspects of work.
  • Must have the ability to maintain confidentiality and handle sensitive information.

Education/Experience

  • Must have a high school diploma or equivalent required; associate degree in healthcare administration, business, or related field preferred.
  • Must have a minimum of 1-3 years of experience in a medical office required, preferably in oncology or a specialty practice.
  • Must be experienced with electronic health records (EHR) and practice management systems.
  • Familiarity with CPT, ICD-10, and HCPCS coding preferred.

Working conditions:

This position works in the business office of a busy outpatient oncology/hematology clinic. This position does not have direct patient contact.

Physical requirements:

This position requires that the employee be able to work at a desk and on a computer for up to eight hours a day. The employee must be able to work via telephone for several hours a day as well.

Direct reports

This position is not a supervisory position.


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