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Clinical Research Associate Jobs in Alabama (NOW HIRING)

Actalent

Part-Time Clinical Research Nurse

Mobile, AL · On-site

$35 - $40/hr

Clinical Research Nurse (Oncology) - Part-Time, Mobile, AL This part-time Clinical Research Nurse position supports an oncology clinical trial at a dedicated research site in Mobile, AL. The nurse ...

MSD

Actively develops and expands the territory for clinical research, finding and developing new sites ... Associate's degree, certificate or equivalent in a scientific / healthcare discipline together with ...

Merck & Co.

Actively develops and expands the territory for clinical research, finding and developing new sites ... Associate's degree, certificate or equivalent in a scientific / healthcare discipline together with ...

Merck & Co.

Actively develops and expands the territory for clinical research, finding and developing new sites ... Associate's degree, certificate or equivalent in a scientific / healthcare discipline together with ...

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All JobsClinical Research Associate JobsClinical Research Associate Jobs in Alabama

Clinical Research Associate information

See Alabama salary details

$10

$37

$63

How much do clinical research associate jobs pay per hour?

As of Aug 14, 2026, the average hourly pay for clinical research associate in Alabama is $37.28, according to ZipRecruiter salary data. Most workers in this role earn between $26.15 and $47.69 per hour, depending on experience, location, and employer.

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 such as a life sciences or healthcare-related field, along with experience in clinical trials. Strong organizational skills, knowledge of Good Clinical Practice (GCP), and familiarity with clinical trial management systems can improve job prospects, but entry may be challenging for those without relevant qualifications or experience.

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 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 the chance to contribute to medical advancements, but it can involve irregular hours and travel. Overall, it can be a rewarding career for those interested in healthcare and research.

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.
More about Clinical Research Associate jobs

What are the most commonly searched types of Clinical Research jobs in Alabama?

The most popular types of Clinical Research jobs in Alabama are:

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For Clinical Research Associate jobs in Alabama, the most frequently searched job titles are:

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The top searched job categories for Clinical Research Associate jobs in Alabama are:

What cities in Alabama are hiring for Clinical Research Associate jobs?

Cities in Alabama with the most Clinical Research Associate job openings:

Clinical Research Associate jobs near you
Infographic showing various Clinical Research Associate job openings in Alabama as of August 2026, with employment types broken down into 77% Full Time, 13% Part Time, and 10% Contract. Highlights an 62% In-person, 6% Hybrid, and 32% Remote job distribution, with an average salary of $77,534 per year, or $37.3 per hour.

Clinical Research Coordinator

No-Resistance Consulting Group

Tuscaloosa, AL • On-site

$22.50 - $25/hr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 2 days ago

New

Job description

Job Location:
Tuscaloosa, AL
Expected Start Date:
October
Company Description:
Headquartered in Birmingham, No Resistance is a clinical trial site management organization that performs clinical trials in urgent care centers throughout the north and southeast. We focus on sample collection and testing trials for lab device manufacturers with the purpose of collecting data to support the device's 510(k) or emergency use approval by the FDA. Notably, the trials we have participated in have directly led to the FDA EUA approval of three separate COVID-19 PCR testing platforms.
No clinical trial experience is required. No Resistance will train the right candidate(s). Hours are Monday-Friday 8:30 am to 5:00 pm with no weekend requirements. Hours may vary based on clinic hours and studies.
Job Description:
No Resistance is seeking motivated individuals to join our team! In this role, you'll play a pivotal part in the implementation and execution of clinical research projects, ensuring the successful attainment of quality, safety, regulatory, and financial objectives.
Job Duties:
  • Maintaining regulatory binders, inventory of study-specific and clinical supplies.
  • Recruiting, and enrolling study subjects.
  • Obtaining informed consent.
  • Collecting nasal swab samples.
  • Testing samples on investigational laboratory PCR analyzers.
  • Data collection and entry.
  • Query resolution.
  • Assuring protocol compliance and efficient workflow including organizing clinical work areas, tracking and ordering study supplies and shipping materials, checking and replacing expired items, etc.

Key Success Factors:
  • Ability to work independently.
  • Desire to work in a clinical environment with direct patient contact.
  • Genuine interest in research.
  • Timely in all communications.
  • Superior attention to detail.

While not a requirement, senior pre-medical students who hope to gain experience in clinical research or recent graduates who have a "gap" year before they start medical school are encouraged to apply. This position offers an exceptional opportunity to earn a competitive income while gaining invaluable experience highly regarded by medical school admission committees.
Job Type: Full-time
Pay:$22.50-$25.00 per hour
Expected hours: 40 per week
Benefits:
  • 401(k)
  • Dental Insurance
  • Health Insurance
  • Paid time off
  • Vision Insurance

Schedule:
  • Monday to Friday

Work Location: In person

Apply