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

As of May 30, 2026, the average hourly pay for cra 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.

What are the key skills and qualifications needed to thrive as a Clinical Research Associate (CRA), and why are they important?

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 (CRAs) 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 are CRA Clinical Research Associates?

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.

Is it hard to get a CRA job?

Securing a CRA (Clinical Research Associate) position can be competitive due to the specialized skills required, such as knowledge of Good Clinical Practice (GCP) and clinical trial processes. Candidates often need relevant education, certifications, and experience in clinical research to improve their chances of obtaining the role.

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 are popular job titles related to Cra Clinical Research Associate jobs in Decatur, GA? For Cra Clinical Research Associate jobs in Decatur, GA, the most frequently searched job titles are:
What job categories do people searching Cra Clinical Research Associate jobs in Decatur, GA look for? The top searched job categories for Cra Clinical Research Associate jobs in Decatur, GA are:
What cities near Decatur, GA are hiring for Cra Clinical Research Associate jobs? Cities near Decatur, GA 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 Decatur, GA as of May 2026, with employment types broken down into 1% As Needed, 63% Full Time, 31% Part Time, and 5% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $83,517 per year, or $40.2 per hour.

Clinical Research Assistant

Metro Infectious Disease Consultants

Decatur, GA • On-site

Other

Medical, Dental, Vision, Life, Retirement, PTO

Posted 3 days ago

Job description

Metro Infusion Center/Metro Infectious Disease Consultants is seeking a Full-Time Clinical Research Assistant who will be responsible for providing non-clinical support in the operations and monitoring of clinical trials. The Research Assistant will analyze and evaluate clinical data gathered during research while ensuring compliance with protocols and overall clinical objectives. Responsibilities assigned to individuals can and will change at any time at the discretion of management or the supervisor

Schedule: Monday-Friday 8:30am-5:00 pm, in-person

Duties:

  • Enter data proficiently and accurately into a data capture system for sponsors and contract research organizations to monitor.
  • Request or acquire the equipment and supplies necessary for each project.
  • Set up, calibrate, and maintain laboratory and/or field research equipment, as specified by the requirements of the study.
  • Assist Clinical Research Associates that are monitoring each study (on and off-site).
  • Invoice for payments associated with the clinical trial budget.
  • Ship lab samples while following regulations and protocols when needed.
  • Attend project meetings and communicate with fellow staff through email and phone calls.
  • Perform ECG's
  • Upload study documents to EMR chart
  • Track specimen shipments
  • Responsibilities may evolve depending on protocol specific requirements

Requirements

  • High school diploma required
  • Bachelor's Degree preferred
  • Proof of current vaccinations, including recommended boosters, commonly required for those working with immunocompromised patients, including measles, mumps, rubella, varicella, hepatitis A & B, influenza.

Requests for accommodations/exceptions will be considered on a case-by-case basis, consistent with applicable laws.

Benefits

  • 401(k)
  • Dental insurance
  • Health insurance
  • Life insurance
  • Paid time off
  • Referral program
  • Vision insurance
  • $50,000-$53,000 ($20/hour + monthly bonus)

Apply