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Entry Level Clinical Research Associate Jobs in Decatur, GA

Alcanza Clinical Research

Part-time Pharm Tech

Decatur, GA · On-site

$17 - $20.75/hr

Adrienne Hilliard Description Alcanza is a growing multi-site, multi-phase clinical research ... An associate's degree and 1+ years' related experience, OR an equivalent combination of education ...

Alcanza Clinical Research

Part-time Pharm Tech

Decatur, GA · On-site

$17 - $20.75/hr

Adrienne Hilliard Description Alcanza is a growing multi-site, multi-phase clinical research ... An associate's degree and 1+ years' related experience, OR an equivalent combination of education ...

Georgia Institute of Technology

Research Assistant

Atlanta, GA · On-site

$18.50 - $25.50/hr

... clinical trial research. OR Associate's degree from an accredited college or university in chemistry, biology, biochemistry, cell biology, social sciences, natural sciences, life, health care, or ...

5 Legal

Health Care Associate

Atlanta, GA · On-site

... clinical research, and/or internal investigations, is preferred. The candidate must be used to and comfortable with working in a team atmosphere and must have excellent academic credentials.

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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.

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

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

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

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

Entry Level Clinical Research Associate jobs near you
Infographic showing various Entry Level 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.

Part-time Pharm Tech

Alcanza Clinical Research

Decatur, GA • On-site

Part-time

Medical, Dental, Vision, Life, Retirement

Posted 20 days ago

Job description

Description
Alcanza is a growing multi-site, multi-phase clinical research company with a network of locations in AL, AZ, FL, GA, IL, MA, MI, MO, NV, VA, SC, TN, TX and Puerto Rico. We have established a strong presence across Phase I-IV studies and several therapeutic areas including vaccine, neurology, dermatology, psychiatry, and general medicine. Join us as we continue to grow.
The Investigational Product Coordinator is responsible for preparing and dispensing study drug, providing drug-related information to subjects and staff in compliance with GCP, ICH, HIPAA, FDA, USP 797, USP 800, state Boards of Pharmacy, and company SOPs.  

Key Responsibilities
Essential Job Duties: 
Under the direction of the Lead Research Pharmacist (or similar) and the Principal/Sub Investigators, conducts the following according to study protocol, company processes & procedures, and in compliance with GCP, ICH, HIPPA, FDA, USP 797, USP 800, state Boards of Pharmacy and company SOPs:
  •  Integration of investigational medication use, pharmacy workflow, subject medication safety activities and regulatory standards;
  •  Coordinating, and advising site staff on drug distribution services for investigational medications;
  •  Identify and justify needs for additional resources, or redeploying resources in new ways to meet needs;
  •  Prepares, labels (if required) and dispenses investigational medications, and provides drug-related information and education for subjects and site staff;
  •  Dispenses controlled substances as part of a research study.  Maintains appropriate inventory records, documentation of receipt and ensures proper storage conditions 
  • Ensures safety and care for all research subjects as it relates to investigational medication preparation and dispensing;
  • Promotes individual professional growth and development by meeting requirements for mandatory/continuing education and skills competency; supports department-based goals which contribute to the success of the organization; serves as mentor and resource to less experienced staff
  • Other duties as assigned.

Skills, Knowledge and Expertise
Minimum Qualifications:  An associate’s degree and 1+ years’ related experience, OR an equivalent combination of education and experience, is required.   Certified Pharmacy Technician (CPhT) credential is required.  Bi-lingual (English / Spanish) proficiency is a plus. 

 Required Skills: 
  • Proficiency with computer applications such as Microsoft applications, email, web applications, 
  • Strong organizational skills and attention to detail.
  • Well-developed interpersonal and listening skills and the ability to work well independently as well as with co-workers, subjects, management, and external customers.
  • Well-developed written and verbal communication skills. 
  • Ability to effectively handle multiple tasks and adapt to changes in workloads and priorities.
  • Must be professional, respectful of others, self-motivated, and have a strong work ethic.
  • Must possess a high degree of integrity and dependability.
  • Ability to work under minimal supervision, identify problems and implement solutions.
  • Ability to handle highly sensitive information in a confidential and professional manner, and in compliance with HIPAA guidelines.

Benefits
  • Full-time employees regularly scheduled to work at least 30 hours per week are benefits-eligible, with coverage starting on the first day of the month following date of hire. 
  • Medical, dental, vision, life insurance, short and long-term disability insurance, health savings accounts, supplemental insurances, and a 401k plan with a safe harbor match are offered.