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Clinical Research Associate Jobs in Decatur, GA (NOW HIRING)

Clinical Research Coordinator III

Atlanta, GA · On-site

$23.25 - $31/hr

Denali Health is a fast-growing clinical research organization dedicated to improving patient outcomes through innovative, high-quality clinical trials. We partner with leading physicians and ...

Clinical Research RN Each of CenExel's research sites specialize in Phase I to Phase IV clinical trials. Our Centers of Excellence comprise some of the most well respected and long-standing research ...

Clinical Research RN Each of CenExel's research sites specialize in Phase I to Phase IV clinical trials. Our Centers of Excellence comprise some of the most well respected and long-standing research ...

Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements. * Proven ability to manage multiple sites and projects ...

... of clinical studies. In over just 30 years, Eurofins has grown from one laboratory in Nantes ... Descripcion del empleo La principal mision del Research Associate sera la de cooperar en un ...

Each of CenExel's research sites specialize in Phase I to Phase IV clinical trials. Our Centers of Excellence comprise some of the most well respected and long-standing research facilities in the ...

Each of CenExel's research sites specialize in Phase I to Phase IV clinical trials. Our Centers of Excellence comprise some of the most well respected and long-standing research facilities in the ...

Each of CenExel's research sites specialize in Phase I to Phase IV clinical trials. Our Centers of Excellence comprise some of the most well respected and long-standing research facilities in the ...

The Clinical Research Coordinator III leads the clinical research program at the site level: effectively recruiting and enrolling research patients under the clinical direction of the principal ...

Clinical Research Coordinator

Morrow, GA · On-site

$23 - $30.75/hr

... clinical research Analytical mindset Attention to detail Exceptional interpersonal skills Superior verbal and written communication skills Understanding of laboratory procedures and equipment ...

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Clinical Research Associate information

See Decatur, GA salary details

$11

$40

$68

How much do clinical research associate jobs pay per hour?

As of Jul 11, 2026, the average hourly pay for clinical research associate in Decatur, GA is $40.15, according to ZipRecruiter salary data. Most workers in this role earn between $28.17 and $51.39 per hour, depending on experience, location, and employer.

Is it hard to get a CRA job?

Securing a Clinical Research Associate (CRA) position can be competitive, often requiring relevant education such as a degree in life sciences or healthcare, along with experience in clinical trials. Strong organizational skills, knowledge of Good Clinical Practice (GCP), and certifications like CCRP can improve job prospects, but entry may still be challenging for those without prior experience or specialized training.

What are Clinical Research Associates?

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, and why are they important?

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.

What is the work of clinical research associate?

A clinical research associate (CRA) monitors clinical trials to ensure they are conducted according to protocols, regulations, and Good Clinical Practice standards. They coordinate with investigators, review trial data, and ensure compliance, often using clinical trial management systems. CRAs typically require knowledge of regulatory requirements and may need certification or training in clinical research.

Is CRA an entry level job?

A Clinical Research Associate (CRA) is typically an entry-level to mid-level position in clinical research, often requiring a bachelor's degree in a related field and some experience or training in clinical trials. Entry-level CRAs may need to complete training on Good Clinical Practice (GCP) and may start as clinical trial assistants or coordinators before advancing to CRA roles.

How do you become a clinical research associate?

To become a clinical research associate (CRA), candidates typically need a bachelor's degree in a health-related field such as life sciences, nursing, or pharmacy. Relevant experience in clinical trials, knowledge of Good Clinical Practice (GCP), and certification from organizations like the Association of Clinical Research Professionals (ACRP) or Society of Clinical Research Associates (SoCRA) can enhance job prospects. CRAs often undergo on-the-job training and may pursue additional certifications to advance their careers.

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 Decatur, GA? The most popular types of Clinical Research jobs in Decatur, GA are:
What are popular job titles related to Clinical Research Associate jobs in Decatur, GA? For Clinical Research Associate jobs in Decatur, GA, the most frequently searched job titles are:
What cities near Decatur, GA are hiring for Clinical Research Associate jobs? Cities near Decatur, GA with the most Clinical Research Associate job openings:

Clinical Research Coordinator III

Denali Health

Atlanta, GA • On-site

$23.25 - $31/hr

Full-time

Medical

Posted 10 days ago


Job description

About Denali Health:
Denali Health is a fast-growing clinical research organization dedicated to improving patient outcomes through innovative, high-quality clinical trials. We partner with leading physicians and sponsors to accelerate breakthrough treatments and foster greater access to research opportunities across diverse communities.
Position Summary:
The Clinical Research Coordinator III (CRC III) is responsible for leading the coordination and execution of complex clinical research studies, ensuring compliance with study protocols, regulatory requirements, and institutional guidelines. The ideal candidate is a proactive professional with strong organizational and leadership skills, capable of managing multiple studies and mentoring junior coordinators.
Key Responsibilities:
  • Coordination of Clinical Trials:
  • Oversee all aspects of assigned clinical studies, including start-up, recruitment, informed consent, data collection, and study close-out. Serve as the primary liaison between investigators, sponsors, CROs, and regulatory agencies.
  • Study Management:
  • Ensure that study activities are conducted in accordance with GCP, IRB guidelines, and sponsor requirements. Maintain accurate and up-to-date source documentation and regulatory binders.
  • Participant Coordination:
  • Schedule and coordinate participant visits, assessments, and follow-ups while maintaining excellent communication and care for study participants.
  • Regulatory and Compliance Oversight:
  • Prepare and submit IRB documents, safety reports, and study updates. Ensure audit readiness at all times.
  • Data Management:
  • Enter, review, and verify data in EDC systems and ensure timely query resolution.
  • Team Coordination & Leadership:
  • Mentor and support CRC I and II staff, ensuring consistent application of best practices and promoting a culture of quality and accountability.
  • Communication & Reporting:
  • Coordinate communication among multidisciplinary teams to ensure efficient trial operations and timely reporting of progress and outcomes.

Qualifications:
  • Bachelor's degree in health sciences, nursing, or a related field (advanced degree preferred).
  • Minimum 3-5 years of experience in clinical research coordination.
  • Strong understanding of GCP, ICH, and FDA regulations.
  • Exceptional coordination, multitasking, and communication skills.
  • Experience with EDC systems and clinical trial management software preferred.
  • CCRC/CCRP certification a plus.

Why Join Denali Health:
  • Work with a mission-driven team advancing clinical research accessibility.
  • Competitive salary and comprehensive benefits package.
  • Professional growth and leadership opportunities.
  • Collaborative environment focused on innovation and patient care.