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Clinical Study Assistant Jobs in Georgia (NOW HIRING)

Sunrise Systems

Clinical Specialist I

Alpharetta, GA · On-site

Maintaining clinical study documents / binder * Scheduling patient appointments * Performing data ... Ability to assist study participants during vision testing procedures. * Ability to lift and move ...

Syneos Health

CRC II (Onsite) - Marietta, GA

Marietta, GA · On-site

$23 - $30.50/hr

... clinical study or federal regulation updates. * Collect and enter study data into the appropriate system. * Coordinate and monitor screening activities; provides support as required. * Assist with ...

MMS

Senior Medical Writer (Remote)

Atlanta, GA · On-site

... that will assist our clients in developing and marketing life-changing therapies to positively ... Substantial clinical study protocol experience, as lead author, required * Experience leading and ...

Peachtree Orthopedics

Clinical Assistant

Duluth, GA · On-site

Clinical Assistant Department: Clinical Services/Practice Operations Reports To: Clinic Manager ... Schedule diagnostic studies and/or surgery; schedule pre- and post-operative appointments.

Peachtree Orthopedics

Clinical Assistant

Cumming, GA · On-site

Clinical Assistant Department: Clinical Services/Practice Operations Reports To: Clinic Manager ... Schedule diagnostic studies and/or surgery; schedule pre- and post-operative appointments.

Artivion

Senior Medical Writer

Kennesaw, GA · On-site

Writing clinical regulatory documents including annual reports, study summaries, and other study ... Support preparation of product IFUs and assist with labeling and labeling changes (including ...

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Clinical Study Assistant information

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How much do clinical study assistant jobs pay per hour?

As of Aug 8, 2026, the average hourly pay for clinical study assistant in Georgia is $17.08, according to ZipRecruiter salary data. Most workers in this role earn between $13.99 and $19.71 per hour, depending on experience, location, and employer.

What are the main challenges a clinical study assistant might face when supporting clinical trial operations?

A Clinical Study Assistant often encounters challenges such as managing multiple tasks under tight deadlines, ensuring accurate documentation, and coordinating communication between research teams, sponsors, and regulatory bodies. Additionally, adapting to evolving study protocols and maintaining compliance with strict regulatory requirements can be demanding. Strong organizational skills, attention to detail, and proactive communication are essential for navigating these challenges successfully.

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

AspectClinical Study AssistantClinical Research Coordinator
CredentialsTypically requires a bachelor's degree in health sciences or related fieldUsually requires a bachelor's degree, often with additional certifications in clinical research
Work EnvironmentSupports clinical trials in hospitals, research centers, or pharmaceutical companiesManages entire clinical studies, coordinating between sites, staff, and sponsors
Employer & IndustryHospitals, research institutions, pharmaceutical companiesAcademic medical centers, hospitals, research organizations
Search & Comparison IntentOften compared for entry-level roles supporting clinical trialsCompared for roles with broader responsibilities in clinical study management

The Clinical Study Assistant primarily supports clinical trial activities by assisting with data collection and documentation, while the Clinical Research Coordinator manages the overall conduct of the study, including patient recruitment and compliance. Both roles require similar educational backgrounds but differ in scope and responsibilities within the clinical research process.

What is a clinical study assistant?

Clinical Study Assistants are professionals who support the conduct of clinical trials by handling administrative tasks, maintaining study documentation, and ensuring regulatory compliance. They work closely with clinical research teams to coordinate schedules, communicate with study sites, and help manage trial materials. Their role is crucial in ensuring that clinical studies run smoothly, efficiently, and according to protocols and regulatory guidelines.

What are the key skills and qualifications needed to thrive as a clinical study assistant?

To thrive as a Clinical Study Assistant, you need strong organizational skills, attention to detail, and a background in life sciences or related fields, often supported by a bachelor's degree. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and regulatory documentation processes is typically required. Effective communication, teamwork, and problem-solving skills help you navigate complex study protocols and collaborate with diverse stakeholders. These abilities are crucial for ensuring the accuracy, compliance, and smooth operation of clinical research studies.
What are the most commonly searched types of Clinical Study jobs in Georgia? The most popular types of Clinical Study jobs in Georgia are:
What cities in Georgia are hiring for Clinical Study Assistant jobs? Cities in Georgia with the most Clinical Study Assistant job openings:
Clinical Study Assistant jobs near you
Infographic showing various Clinical Study Assistant job openings in Georgia as of July 2026, with employment types broken down into 2% As Needed, 75% Full Time, 15% Part Time, 1% Temporary, 6% Contract, and 1% Nights. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $35,531 per year, or $17.1 per hour.

Clinical Research Assistant

Metro Infectious Disease Consultants

Decatur, GA

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 14 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