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Contract Clinical Research Associate Jobs in Decatur, GA

Actalent

Clinical Research Coordinator

Atlanta, GA · On-site

$22 - $25/hr

This contract role focuses on patient-facing coordination, data entry, and logistical support for ... Clinical research experience, including at least one year in a clinical research setting; academic ...

CVAUSA

Clinical Research Coordinator

Tucker, GA · On-site

$60 - $80/hr

Clinical Research Coordinator Location: Tucker, Ga Job Type: Full-time This is an onsite position ... Associates of America (CVAUSA) is a rapidly growing leader in cardiovascular care, committed to ...

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Alcanza

Clinical Research Coordinator

Decatur, GA

$23.75 - $31.50/hr

A Medical Assistant diploma, LPN/LVN, EMT credential OR Associate's degree AND a minimum of 1 year of clinical research or clinical experience, OR an equivalent combination of education and ...

Alcanza

Clinical Research Coordinator

Decatur, GA

$23.75 - $31.50/hr

A Medical Assistant diploma, LPN/LVN, EMT credential OR Associate's degree AND a minimum of 1 year of clinical research or clinical experience, OR an equivalent combination of education and ...

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All JobsContract Clinical Research Associate JobsContract Clinical Research Associate Jobs in Decatur, GA

Contract Clinical Research Associate information

See Decatur, GA salary details

$10

$34

$59

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

As of Sep 3, 2026, the average hourly pay for contract clinical research associate in Decatur, GA is $34.85, according to ZipRecruiter salary data. Most workers in this role earn between $24.42 and $44.62 per hour, depending on experience, location, and employer.

What is a contract clinical research associate?

Contract Clinical Research Associates (CRAs) are professionals who monitor clinical trials on behalf of pharmaceutical companies, contract research organizations (CROs), or other sponsors, but work on a contract or freelance basis rather than as permanent employees. Their primary responsibilities include ensuring that trials are conducted according to regulatory guidelines, monitoring data accuracy, and verifying that patient rights and safety are protected. Contract CRAs may work on multiple projects for different clients and often enjoy more flexibility in their schedules and work locations. This role requires strong organizational skills, knowledge of Good Clinical Practice (GCP), and the ability to travel to clinical sites.

What are some of the unique challenges faced by contract clinical research associates compared to permanent employees?

Contract Clinical Research Associates often need to quickly adapt to new study protocols, sponsor requirements, and team dynamics since they may work on multiple projects for different organizations. This can mean a faster onboarding process and the need to build rapport with new colleagues and site staff efficiently. Additionally, contract CRAs must be highly organized to manage shifting assignments and maintain compliance across different trial sites, as well as keep up with varying documentation standards. While this variety can be rewarding, it can also present challenges in terms of consistency and long-term project ownership.

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

To thrive as a Contract Clinical Research Associate, you need a solid understanding of clinical trial protocols, regulatory guidelines (such as GCP and ICH), and typically a degree in life sciences or related field. Familiarity with electronic data capture (EDC) systems, clinical trial management systems (CTMS), and certifications like ACRP or SOCRA are highly valued. Strong attention to detail, organizational skills, and effective communication help build productive site relationships and ensure compliance. These skills are crucial for maintaining data integrity, ensuring regulatory adherence, and supporting successful clinical trial outcomes.

What is the difference between Contract Clinical Research Associate vs Clinical Research Associate?

AspectContract Clinical Research AssociateClinical Research Associate
CredentialsTypically requires a degree in life sciences and relevant certificationsSame as Contract CRA, often with additional experience
Work EnvironmentTemporary, project-based assignments often with multiple sponsorsFull-time employment with a single organization or sponsor
Employer & Industry UsageUsed by CROs and pharma companies for short-term projectsCommonly employed directly by pharmaceutical companies or CROs
Search & Comparison IntentOften compared for flexibility and contract work benefitsViewed as a permanent role with career growth

In summary, Contract Clinical Research Associates work on temporary, project-specific basis, often with multiple sponsors, offering flexibility. Clinical Research Associates typically hold full-time roles within a single organization, providing stability and career development opportunities.

What are popular job titles related to Contract Clinical Research Associate jobs in Decatur, GA?

For Contract Clinical Research Associate jobs in Decatur, GA, the most frequently searched job titles are:

What job categories do people searching Contract Clinical Research Associate jobs in Decatur, GA look for?

The top searched job categories for Contract Clinical Research Associate jobs in Decatur, GA are:

What cities near Decatur, GA are hiring for Contract Clinical Research Associate jobs?

Cities near Decatur, GA with the most Contract Clinical Research Associate job openings:

Contract Clinical Research Associate jobs near you
Infographic showing various Contract Clinical Research Associate job openings in Decatur, GA as of August 2026, with employment types broken down into 1% As Needed, 68% Full Time, 29% Part Time, 1% Temporary, and 1% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $83,517 per year, or $40.2 per hour.

Clinical Research Coordinator

Cardiovascular Associates of America

Tucker, GA • On-site

$22.75 - $30.50/hr

Full-time

Posted 9 days ago

Job description

Clinical Research Coordinator
Location: Tucker, Ga
Job Type: Full-time
This is an onsite position in Tucker, Georgia
About CVAUSA
Cardiovascular Associates of America (CVAUSA) is a rapidly growing leader in cardiovascular care, committed to advancing medical research and improving patient outcomes. As part of our expansion, we are increasing our clinical trial operations and are seeking dynamic, results-driven professionals to join our team in Tucker, Ga.
At CVAUSA, we are focused on innovation and excellence in cardiovascular research, and we believe the best results come from individuals who are passionate about making a difference.
We are hiring a Clinical Research Coordinator for the Tucker, Ga. office. The Clinical Research Coordinator will be responsible for supporting the growth and development of the research program while collaborating with clinic staff on existing and new clinical trials. As part of CVAUSA's national network, this role offers the opportunity to collaborate with teams across the country and make an impact both locally and nationwide.
Position Overview
As a Clinical Research Coordinator, you will play a key role in coordinating and overseeing clinical trials and supporting site operations. You will have the opportunity to manage your studies with a high degree of autonomy while working closely with investigators, sponsors, and site staff. This is an excellent opportunity for a motivated, detail-oriented individual who thrives in a fast-paced environment.
Key Responsibilities
Clinical Trial Coordination
Coordinate all aspects of clinical trials, including patient recruitment, screening, enrollment, and follow-up visits. Ensure study protocols are followed accurately and consistently.
Site Operations
Support day-to-day research site operations while ensuring compliance with regulatory requirements and study protocols.
Data Management
Collect, verify, and maintain clinical trial data, ensuring accuracy, completeness, and timely entry.
Communication & Reporting
Serve as a primary point of contact for study sponsors, participants, and research stakeholders. Provide regular study updates and assist with reporting requirements.
Regulatory Compliance
Maintain up-to-date study documentation, regulatory binders, and patient records in compliance with GCP, ICH guidelines, and applicable regulations.
Process Improvement
Assist with identifying opportunities to improve research workflows and enhance study performance.
What We're Looking For
Detail-Oriented & Organized
Able to manage multiple priorities while maintaining a high level of accuracy and quality.
Strong Communicator
Effectively communicates with sponsors, investigators, site staff, and participants.
Collaborative Team Player
Works well independently and as part of a multidisciplinary team.
Adaptable & Results-Oriented
Thrives in a dynamic environment and remains focused on achieving study goals.
Experience & Qualifications
  • Clinical experience in cardiovascular medicine in a licensed role (e.g., RN, technologist, medical assistant, etc.)
  • Bachelor's degree in a relevant field (life sciences, healthcare, or clinical research) preferred
  • Minimum of 1-2 years of clinical research experience, including patient enrollment and study coordination
  • Strong organizational and time management skills
  • Clinical research certification (e.g., CCRP) preferred
  • Knowledge of GCP, ICH guidelines, and regulatory requirements
  • Experience with electronic data capture systems and regulatory documentation preferred
Why CVAUSA?
At CVAUSA, we believe in the power of innovation and are looking for professionals eager to make an impact in cardiovascular research. As part of our growing organization, you'll be at the forefront of cutting-edge clinical trials.

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