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Clinical Research Associate information

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$10

$36

$62

How much do clinical research associate jobs pay per hour?

As of Aug 29, 2026, the average hourly pay for clinical research associate in Madison, AL is $36.85, according to ZipRecruiter salary data. Most workers in this role earn between $25.87 and $47.16 per hour, depending on experience, location, and employer.

What is a clinical research associate?

Clinical Research Associates (CRAs) are professionals responsible for monitoring and overseeing clinical trials to ensure they are conducted in accordance with regulatory guidelines, protocols, and ethical standards. They play a key role in ensuring the safety of trial participants and the integrity of collected data. CRAs often visit clinical trial sites to verify data accuracy, maintain study documentation, and provide training to site staff. Their work ensures that new drugs, treatments, or medical devices are tested rigorously before they reach the market.

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

To thrive as a Clinical Research Associate, you need a solid background in life sciences, attention to detail, and experience with clinical trial protocols, often supported by a relevant bachelor's degree. Familiarity with electronic data capture (EDC) systems, Good Clinical Practice (GCP) guidelines, and sometimes certifications like ACRP or SOCRA is typically required. Strong organizational, communication, and problem-solving skills help build effective relationships with research sites and ensure compliance. These skills are vital for maintaining the integrity of clinical trials, ensuring regulatory adherence, and advancing medical research efficiently.

What are some common challenges clinical research associates face when monitoring clinical trial sites?

Clinical Research Associates (CRAs) often encounter challenges such as ensuring protocol compliance across multiple sites, managing tight project timelines, and maintaining accurate documentation. Additionally, CRAs must effectively communicate with site staff to resolve issues and ensure data integrity, all while adhering to regulatory guidelines. Balancing frequent travel, adapting to different site environments, and handling unexpected issues such as patient recruitment delays are also typical aspects of the role.

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

AspectClinical Research AssociateClinical Trial Coordinator
CredentialsBachelor's degree, often with clinical research certificationsBachelor's degree, often with clinical research or healthcare certifications
Work EnvironmentMonitors clinical sites, reviews data, ensures complianceCoordinates trial activities, manages schedules, and communicates with sites
Employer & IndustryPharmaceutical companies, CROs, biotech firmsHospitals, research institutions, CROs

Both roles are essential in clinical trials, with CRAs focusing on site monitoring and compliance, while Clinical Trial Coordinators handle day-to-day trial management. They often collaborate but have distinct responsibilities within the clinical research process.

Is being a clinical research associate worth it?

A clinical research associate (CRA) monitors clinical trials to ensure compliance with protocols and regulations, often requiring strong organizational and communication skills. The role offers opportunities for career growth, competitive salaries, and work in the healthcare or pharmaceutical industries, but it can involve irregular hours and travel. Overall, it can be a rewarding career for those interested in medical research and patient safety.

Is it hard to get a clinical research associate job?

Securing a clinical research associate (CRA) position can be competitive, often requiring a relevant degree in life sciences or healthcare, along with experience in clinical trials. Strong organizational skills, knowledge of Good Clinical Practice (GCP), and familiarity with trial management tools can improve job prospects, but entry-level roles may be easier to obtain with relevant internships or certifications.
More about Clinical Research Associate jobs

What are the most commonly searched types of Clinical Research jobs in Madison, AL?

The most popular types of Clinical Research jobs in Madison, AL are:

What job categories do people searching Clinical Research Associate jobs in Madison, AL look for?

The top searched job categories for Clinical Research Associate jobs in Madison, AL are:

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

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

Clinical Research Associate jobs near you
Infographic showing various Clinical Research Associate job openings in Madison, AL as of August 2026, with employment types broken down into 100% Full Time. Highlights an 91% In-person, and 9% Remote job distribution, with an average salary of $76,643 per year, or $36.8 per hour.

Clinical Research Assistant

Medovation Clinical Research LLC

Huntsville, AL • On-site

$20/hr

Full-time

Re-posted 27 days ago

Job description

Full-Time | Huntsville, AL

Launch Your Career in Clinical Research

Medovation Clinical Research is seeking an experienced, motivated Clinical Research Assistant to join our growing team in Huntsville, Alabama. This position offers the opportunity to work alongside physicians and research professionals conducting cutting-edge clinical trials that improve patient care and advance medicine.
Position Summary
The Clinical Research Assistant supports the successful execution of clinical trials by assisting with patient visits, study procedures, data collection, regulatory documentation, and participant recruitment while ensuring compliance with FDA regulations and Good Clinical Practice (GCP).
Responsibilities
  • Assist research coordinators and investigators with clinical trial visits
  • Recruit, schedule, and follow up with study participants
  • Collect and accurately document clinical research data
  • Maintain study files and regulatory documentation
  • Prepare study materials and laboratory specimens
  • Ensure compliance with study protocols and GCP guidelines
Qualifications
  • Minimum of 1 year of clinical research experience preferred
  • Bachelor's degree or healthcare-related experience preferred - premed and gap year med students encouraged
  • Strong organizational, communication, and computer skills
  • Ability to work independently in a fast-paced clinical environment
  • Experience with electronic medical records and research documentation is a plus
Why Join Medovation?
  • Competitive salary and benefits
  • Opportunity for career advancement
  • Work directly with experienced investigators and research professionals
  • Be part of a growing, mission-driven organization dedicated to bringing innovative therapies to patients
  • Support a collaborative team committed to excellence in clinical research
If you are detail-oriented, patient-focused, and passionate about advancing healthcare through clinical research, we'd love to hear from you.