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Entry Level Clinical Research Associate Jobs in Decatur, GA

CVAUSA

Clinical Research Coordinator

Tucker, GA · On-site

$22.75 - $30.50/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 ...

Alcanza

Clinical Research Coordinator

Decatur, GA · On-site

$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 · On-site

$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 ...

Eurofins Scientific

RESEARCH ASSOCIATE

Atlanta, GA · On-site

... 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 ...

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Entry Level Clinical Research Associate information

What is an entry level clinical research associate?

An Entry Level Clinical Research Associate (CRA) is responsible for monitoring clinical trials to ensure compliance with regulatory requirements, ethical guidelines, and study protocols. They assist in site selection, data collection, and verifying that study procedures are properly followed. Entry-level CRAs typically work under the supervision of senior CRAs and may travel to different clinical sites. Strong attention to detail, knowledge of Good Clinical Practice (GCP) guidelines, and organizational skills are essential. This role is a starting point for a career in clinical research, with opportunities for growth into senior CRA or project management positions.

What are the typical daily responsibilities of an entry level clinical research associate?

As an Entry Level Clinical Research Associate, your day-to-day work generally involves assisting with monitoring clinical trial sites, reviewing study documentation, and ensuring adherence to protocol and regulatory requirements. You may support more senior team members in conducting on-site or remote visits, tracking patient recruitment, and managing data collection. Additionally, you’ll communicate regularly with site staff and other stakeholders to resolve issues and ensure data quality. This hands-on experience is essential for building expertise in clinical research processes and advancing toward more senior CRA roles.

What are the key skills and qualifications needed to thrive as an entry level clinical research associate?

To thrive as an Entry Level Clinical Research Associate, you typically need a bachelor's degree in life sciences or a related field, a solid understanding of clinical trial protocols, and attention to detail. Familiarity with Good Clinical Practice (GCP) guidelines, electronic data capture (EDC) systems, and regulatory documentation is often required. Strong communication, organization, and problem-solving abilities help you effectively collaborate with study sites and team members. These skills are critical to ensure the accuracy, compliance, and successful progression of clinical studies.

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

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Entry Level Clinical Research Associate jobs near you
Infographic showing various Entry Level Clinical Research Associate job openings in Decatur, GA as of September 2026, with employment types broken down into 3% As Needed, 74% Full Time, 15% Part Time, and 8% Contract. Highlights an 87% Physical, 1% Hybrid, and 12% Remote job distribution.

Clinical Research Coordinator

Tucker, GA • On-site

Cardiovascular Associates of America
Health Care and Social Assistance • 51 - 200 employees
Learn more about Cardiovascular Associates of Americaexternal

$22.75 - $30.50/hr

Full-time

Posted 18 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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