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

Alcanza

Clinical Research Coordinator

Decatur, GA

$23.75 - $31.50/hr

The Clinical Research Coordinator (CRC) works to ensure the execution of assigned studies in ... studies. Minimum Qualifications : A Medical Assistant diploma, LPN/LVN, EMT credential OR Associate ...

ICON

Senior Clinical Research Associate

Atlanta, GA · On-site +1

Senior Clinical Research Associate - Cardio (Smartpulse A-fib) - All Regions ICON is a global ... A well-executed plan for communication with the study teams and sites. * Well-versed in clinical ...

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How much do clinical study associate jobs pay per hour?

As of May 30, 2026, the average hourly pay for clinical study associate in Decatur, GA is $30.79, according to ZipRecruiter salary data. Most workers in this role earn between $20.67 and $40.62 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Clinical Study Associate, and why are they important?

To thrive as a Clinical Study Associate, you need a strong understanding of clinical research processes, regulatory requirements, and typically a life sciences degree. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and GCP certification are commonly required. Attention to detail, organizational skills, and effective communication set top performers apart in this role. These competencies ensure accurate study documentation, regulatory compliance, and smooth coordination across research teams.

What are some common challenges Clinical Study Associates face when managing multiple clinical trials simultaneously?

Clinical Study Associates often juggle several clinical trials at once, which can present challenges such as prioritizing competing deadlines, maintaining accurate documentation for each study, and ensuring consistent communication with cross-functional teams. Staying organized and proactive is essential, as unforeseen protocol amendments or site issues can arise. Building strong relationships with site staff and utilizing effective project management tools can help CSAs navigate these complexities and deliver high-quality results.

What are Clinical Study Associates?

Clinical Study Associates (CSAs) are professionals who support the planning, execution, and monitoring of clinical trials in the pharmaceutical, biotechnology, or medical device industries. They help coordinate study logistics, maintain study documentation, and ensure compliance with regulatory requirements. CSAs often work closely with Clinical Research Associates, study coordinators, and investigators to ensure that trials are conducted according to protocol and timelines. Their role is essential in ensuring the accuracy and integrity of data collected during clinical research.

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

AspectClinical Study AssociateClinical Research Coordinator
CredentialsBachelor's degree, often in life sciences; certifications like CCRP or CCRA beneficialBachelor's degree in health sciences or related field; certifications like CCRP advantageous
Work EnvironmentPharmaceutical companies, CROs, clinical trial sitesHospitals, clinics, research centers
Job FocusMonitoring clinical trials, ensuring protocol compliance, data accuracyManaging daily trial activities, patient recruitment, data collection
Employer & Industry UsageCommonly employed in pharma and CROsPrimarily in healthcare and academic research settings

Both roles involve clinical trial oversight but differ in focus: Clinical Study Associates primarily monitor and ensure compliance during trials, while Clinical Research Coordinators manage daily trial operations and patient interactions. Understanding these distinctions helps in choosing the right career path or job search focus.

What are the most commonly searched types of Clinical Study jobs in Decatur, GA? The most popular types of Clinical Study jobs in Decatur, GA are:
What are popular job titles related to Clinical Study Associate jobs in Decatur, GA? For Clinical Study Associate jobs in Decatur, GA, the most frequently searched job titles are:
What job categories do people searching Clinical Study Associate jobs in Decatur, GA look for? The top searched job categories for Clinical Study Associate jobs in Decatur, GA are:
What cities near Decatur, GA are hiring for Clinical Study Associate jobs? Cities near Decatur, GA with the most Clinical Study Associate job openings:
Clinical Study Associate jobs near you

Clinical Research Assistant

Metro Infectious Disease Consultants

Decatur, GA • On-site

Full-time

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)