ZipRecruiter

Log In

1

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

Alcanza

Clinical Research Coordinator

Decatur, GA · On-site

$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 ...

Eurofins Scientific

RESEARCH ASSOCIATE

Atlanta, GA

... 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 ...

DelRicht Research

Clinical Research Coordinator

Atlanta, GA

$23.25 - $31/hr

... study execution across our clinics, ensuring: * Patients have a positive, professional, and ... Bachelor's or Associate's degree from an accredited college or university. * Preferred: Active RMA ...

New

DelRicht Research

Clinical Research Coordinator

Decatur, GA

$23.25 - $30.75/hr

... study execution across our clinics, ensuring: * Patients have a positive, professional, and ... Bachelor's or Associate's degree from an accredited college or university. * Preferred: Active RMA ...

New

next page

Showing results 1-20

All JobsClinical Study Associate JobsClinical Study Associate Jobs in Decatur, GA

Clinical Study Associate information

See Decatur, GA salary details

$12

$30

$53

How much do clinical study associate jobs pay per hour?

As of Jul 13, 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 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 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 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 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
Infographic showing various Clinical Study Associate job openings in Decatur, GA as of July 2026, with employment types broken down into 1% As Needed, 66% Full Time, 29% Part Time, 2% Temporary, and 2% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $64,051 per year, or $30.8 per hour.
Ophthalmic Research Assistant - Vision Care (278429)

Ophthalmic Research Assistant - Vision Care (278429)

ASK Consulting

Johns Creek, GA • On-site

$25 - $30/hr

Contractor

This job post has expired today. Applications are no longer accepted.

Job description

"All candidates must be directly contracted by ASK Consulting on their payroll and cannot be subcontracted. We are unable to provide sponsorship at this moment".


Job Title: Ophthalmic Research Assistant - Vision Care

Location: Johns Creek, GA 30097 (onsite)

Duration: 12 months

Pay Rate : $25 -$30/hr.

Interviews: 2

Important Notes: 

  • Can work up to 40 hours a week (typical hours will range between 25-30 hours)
  • Schedule: 9:00 AM 5:00 PM EST
  • Rotating days possible and contingent upon subject availability


Job Description:

  • This position is responsible for conducting data collection to support ongoing research studies.
  • Additional duties include scheduling appointments, managing research data and records, and collaborating closely with the Vision Scientist to prepare qualification documents for new ophthalmic devices.


Essential Duties and Responsibilities:

The essential functions of this role include, but are not limited to:

  • Collecting data from human subjects for research purposes
  • Maintaining clinical study documents / binder
  • Scheduling patient appointments
  • Performing data entry into computer systems
  • Managing recruitment and follow-up of research participants
  • Maintaining an organized and clean research laboratory workspace
  • Assisting the team in the preparation of qualification and validation documentation for new ophthalmic devices
  • Tracking progress and providing weekly communication updates and feedback to the manager to ensure swift and prompt resolution of any issues


Minimum Qualifications (Knowledge, Skills and Abilities:

  • High School Diploma required
  • Experience with patient-facing interaction preferred
  • Proficiency in basic computer skills and data entry


Preferred Qualifications:

  • Preferred experience with fundamental ophthalmic tests
  • Visual acuity (VA)
  • Contrast sensitivity (CSF)
  • Refraction and over-refraction
  • Binocular vision testing
  • Color vision assessments
  • Preferred experience in preparing documentation such as qualifications, user manuals, and operating procedures for new ophthalmic devices


Physical Requirements:

  • Ability to sit, stand, and operate laboratory equipment for extended periods.
  • Ability to assist study participants during vision testing procedures.
  • Ability to lift and move equipment weighing up to 25pounds.


About ASK: ASK Consulting is an award-winning technology and professional services recruiting firm servicing Fortune 500 organizations nationally. With 5 nationwide offices, two global delivery centers, and employees in 42 states-ASK Consulting connects people with amazing opportunities

ASK Consulting is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all associates.