ZipRecruiter

Log In

1

Senior Clinical Research Associate Jobs in Decatur, GA

Denali Health

Clinical Research Nurse

Atlanta, GA · On-site

We are seeking an experienced Clinical Research Nurse to join our Atlanta team on a PRN basis. This position offers flexible scheduling while providing critical support to our clinical trial ...

Denali Health

Clinical Research Nurse

Atlanta, GA · On-site

We are seeking an experienced Clinical Research Nurse to join our Atlanta team on a PRN basis. This position offers flexible scheduling while providing critical support to our clinical trial ...

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 ...

Actalent

Clinical Research Coordinator

Atlanta, GA

$22 - $25/hr

Clinical Research Coordinator The Clinical Research Coordinator will support a post-market respiratory testing study consisting of single study visits of approximately one hour. This contract role ...

previous pagenext page

Showing results 21-40

All JobsClinical Research Associate JobsSenior Clinical Research Associate JobsSenior Clinical Research Associate Jobs in Decatur, GA

Senior Clinical Research Associate information

See Decatur, GA salary details

$35.1K

$92.1K

$140.1K

How much do senior clinical research associate jobs pay per year?

As of Aug 28, 2026, the average yearly pay for senior clinical research associate in Decatur, GA is $92,082.00, according to ZipRecruiter salary data. Most workers in this role earn between $61,000.00 and $125,000.00 per year, depending on experience, location, and employer.

What does a senior clinical research associate do?

A senior clinical research associate (CRA) monitors clinical trials and manages team members. Your duties include leading project team meetings, running experiments, making observations, tracking results, and analyzing data. You also ensure experiments meet all clinical practice and safety standards. Qualifications for this career are a bachelor of science in a biomedical field or a bachelor of science in nursing (BSN), along with professional experience in a medical or research setting. You must have strong communication, interpersonal, leadership, and technical writing skills.

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

To thrive as a Senior Clinical Research Associate, you need a solid background in clinical research, regulatory compliance, and often a degree in life sciences or a related field. Familiarity with electronic data capture (EDC) systems, Good Clinical Practice (GCP) guidelines, and relevant certifications such as ACRP or SOCRA are typically required. Strong organizational skills, attention to detail, and the ability to communicate effectively with diverse stakeholders make someone stand out in this position. These skills and qualities are vital for ensuring studies are conducted ethically, accurately, and in compliance with regulatory standards.

What are some typical challenges faced by senior clinical research associates when overseeing multiple clinical trials?

Senior Clinical Research Associates (SCRAs) often manage several studies at once, which requires balancing competing deadlines, ensuring protocol compliance, and maintaining strong communication with site staff. A common challenge is ensuring consistent data quality and regulatory adherence across diverse sites, especially when trials are geographically dispersed. Effective time management, attention to detail, and proactive problem-solving are crucial for success in this role. Collaboration with project managers, investigators, and regulatory teams is also essential to ensure trials progress smoothly and meet all regulatory requirements.
More about Senior Clinical Research Associate jobs

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

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

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

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

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

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

Senior Clinical Research Associate jobs near you
Infographic showing various Senior Clinical Research Associate job openings in Decatur, GA as of August 2026, with employment types broken down into 2% As Needed, 74% Full Time, 18% Part Time, and 6% Contract. Highlights an 85% Physical, 1% Hybrid, and 14% Remote job distribution, with an average salary of $92,082 per year, or $44.3 per hour.

Clinical Research Coordinator

Cardiovascular Associates of America

Tucker, GA • On-site

$22.75 - $30.50/hr

Full-time

Posted 2 days ago

New

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 ResponsibilitiesClinical 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 ForDetail-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.

Powered by JazzHR

hJTD0Xgm1t