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Clinical Trials Associate Jobs in Georgia (NOW HIRING)

Emory University

Pediatric BMT Clinician

Atlanta, GA

$165K - $214K/yr

Rank of assistant or associate professor will depend on experience and accomplishments. About the ... Aflac is a member of the COG Pediatric Early Phase Clinical Trials Network (PEP-CTN), NANT, TACL ...

Emory University

Pediatric BMT Clinician

Atlanta, GA · On-site

$165K - $214K/yr

Rank of assistant or associate professor will depend on experience and accomplishments. About the ... Aflac is a member of the COG Pediatric Early Phase Clinical Trials Network (PEP-CTN), NANT, TACL ...

Emory University

Pediatric BMT Clinician

Atlanta, GA · On-site

$165K - $214K/yr

Rank of assistant or associate professor will depend on experience and accomplishments. About the ... Aflac is a member of the COG Pediatric Early Phase Clinical Trials Network (PEP-CTN), NANT, TACL ...

SOMPI: BMT

Job Pediatric BMT Clinician

Atlanta, GA · On-site

Rank of assistant or associate professor will depend on experience and accomplishments. About the ... Aflac is a member of the COG Pediatric Early Phase Clinical Trials Network (PEP-CTN), NANT, TACL ...

Becton, Dickinson and Company

The clinical trials may be of moderate scope and complexity. Use programming knowledge to develop ... At BD, we are committed to supporting our associates' well-being, development, and success through ...

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Clinical Trials Associate information

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$14

$33

$59

How much do clinical trials associate jobs pay per hour?

As of Aug 12, 2026, the average hourly pay for clinical trials associate in Georgia is $33.76, according to ZipRecruiter salary data. Most workers in this role earn between $27.21 and $37.16 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a clinical trials associate, and why are they important?

To thrive as a Clinical Trials Associate, you need a solid understanding of clinical research protocols, regulatory compliance, and data management, typically supported by a life sciences degree. Familiarity with systems such as electronic data capture (EDC), clinical trial management systems (CTMS), and knowledge of Good Clinical Practice (GCP) guidelines or related certifications is important. Strong organizational skills, attention to detail, and effective communication help you excel in coordinating study activities and collaborating with diverse teams. These skills ensure accurate trial execution, regulatory adherence, and successful study outcomes.

What do I need to be a clinical trials associate?

To become a clinical trials associate, candidates typically need a bachelor's degree in life sciences, healthcare, or a related field. Relevant skills include knowledge of Good Clinical Practice (GCP), attention to detail, and experience with clinical trial management systems; certifications like CCRP can be advantageous.

What are some common challenges faced by clinical trials associates, and how can they be managed effectively?

Clinical Trials Associates often face challenges such as coordinating with multiple stakeholders, managing tight deadlines, and ensuring strict compliance with regulatory guidelines. Balancing administrative tasks with participant communication requires strong organizational skills and attention to detail. Staying proactive in communication, utilizing project management tools, and seeking guidance from senior team members can help manage these challenges effectively while fostering a collaborative team environment.

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

AspectClinical Trials AssociateClinical Research Coordinator
CredentialsBachelor's degree, often in life sciences; certifications like ACRP or SOCRA are commonBachelor's degree in health sciences or related field; certifications like CCRP are advantageous
Work EnvironmentTypically works in clinical trial sites, pharmaceutical companies, or CROsWorks directly at clinical sites, hospitals, or research centers
Job FocusSupports trial setup, data entry, and regulatory complianceManages patient recruitment, scheduling, and data collection

While both roles support clinical research, Clinical Trials Associates primarily focus on trial logistics and compliance, whereas Clinical Research Coordinators handle patient interactions and site management. Both positions require similar educational backgrounds and certifications, often working in the same environments, but their daily responsibilities differ.

What is a clinical trials associate?

Clinical Trials Associates (CTAs) are professionals who support the planning, coordination, and administration of clinical research studies, often working under the supervision of Clinical Research Coordinators or Managers. Their responsibilities typically include maintaining study documentation, ensuring regulatory compliance, assisting with data collection, and communicating with study sites. CTAs play a critical role in ensuring that clinical trials run smoothly and adhere to strict protocols and guidelines. Their work helps bring new medical treatments and therapies to market safely and efficiently.
What are the most commonly searched types of Clinical Trials jobs in Georgia? The most popular types of Clinical Trials jobs in Georgia are:
What cities in Georgia are hiring for Clinical Trials Associate jobs? Cities in Georgia with the most Clinical Trials Associate job openings:
Clinical Trials Associate jobs near you
Infographic showing various Clinical Trials Associate job openings in Georgia as of August 2026, with employment types broken down into 2% As Needed, 72% Full Time, 18% Part Time, 1% Temporary, and 7% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $70,227 per year, or $33.8 per hour.

Clinical Research Quality Control Associate

CenExel

Decatur, GA • On-site

Full-time

Medical, Dental, Vision, Life, Retirement

Re-posted 17 days ago

CenExel rating

7.5

Company rating: 7.5 out of 10

Based on 6 frontline employees who took The Breakroom Quiz

64th of 120 rated laboratories

Job description

About Us:
CenExel is a leading nationwide clinical research site and patient network serving the life sciences industry. Leading in CNS and early phase studies, our 18 science-led Centers of Excellence deliver the right patients, at the right time, in the right place. Recently acquired by BayPine Capital Partners, our research sites provide unparalleled medical and scientific support in the design and execution of clinical trials. Our world-class PIs, advanced patient engagement strategies, premium data analytics, and integrated operations optimize every step of the clinical trial process.
Along with an exceptional work environment that promotes teamwork, positive leadership, and optimal work-life balance, CenExel Clinical Research also provides highly competitive compensation and a generous benefits package to full time employees after 30 days of employment including Health Insurance, Dental, Vision, LTD, STD, Life Ins, and 401k.
Job Summary:
The Clinical Research Quality Control (QC) Associate is responsible for ensuring the accuracy, consistency, and integrity of clinical trial documentation and processes. Working closely with clinical operations, data management, and regulatory teams, the QC Associate reviews essential trial documents and clinical data to verify compliance with GCP (Good Clinical Practice), ICH guidelines, regulatory requirements, and internal SOPs.
Essential Responsibilities and Duties:
  • Performs quality control reviews of clinical trial documents (e.g., informed consent forms, case report forms, regulatory binders, monitoring visit reports) to ensure accuracy, completeness, and consistency.
  • Identifies discrepancies, deviations, or data entry errors and follow up with appropriate teams for resolution.
  • Supports the preparation and QC of Trial Master File (TMF) documents (paper and/or electronic).
  • Assists in internal audits and inspection readiness activities.
  • Collaborates with cross-functional teams (clinical operations, data management, regulatory affairs) to maintain high standards in documentation practices.
  • Maintains and tracks QC metrics and contribute to quality improvement initiatives.
  • Ensures that all clinical documentation complies with GCP, ICH, FDA, EMA, and company SOPs.
  • Assists with SOP development and updates related to quality control activities.
  • Supports and ensures strictest adherence to best practices, FDA Code of Federal Regulations, ICH (International Conference on Harmonization), GCP (Good Clinical Practices), CenExel standard operating procedures, site working Practices, protocol, and company guidelines and policies.
  • Assumes other duties and responsibilities as assigned. The above responsibilities are a general description of the level and nature of the work assigned to this classification and are not to be considered as all inclusive.

Education/Experience/Skills:
  • Must be able to effectively communicate verbally and in writing.
  • Bachelor's degree in life sciences, healthcare, or a related field required. Advanced degree preferred.
  • 1-3 years of experience in clinical research, with at least 1 year in a QC, QA, or documentation review role.
  • Familiarity with clinical trial processes and regulatory requirements (GCP, ICH, FDA, EMA).
  • Experience with electronic systems such as eTMF, EDC, and CTMS preferred.
  • Strong attention to detail and organizational skills.
  • Excellent written and verbal communication.
  • Ability to work independently and in a team-oriented environment.
  • Proficiency in Microsoft Office (Word, Excel, Outlook, PowerPoint).
  • Certification in clinical research (e.g., ACRP, SOCRA) is a plus.
  • Experience in Phase I-IV trials or in a CRO environment.

Working Conditions
  1. Indoor, Office environment.
  2. Indoor, Clinic environment.
  3. Essential physical requirements include sitting, typing, standing, and walking.
  4. Lightly active position, occasional lifting of up to 20 pounds.
  5. Reporting to work, as scheduled, is essential.
  6. Occasional travel may be required (e.g., for audits or training).

CenExel Clinical Research is an Equal Opportunity Employer. All applicants will be considered for employment without regards to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran, or status.
Equal Opportunity Employer
This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor.

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