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Clinical Project Associate Jobs in Georgia (NOW HIRING)

Agilent

Clinical Affairs Scientist

Turin, GA · On-site +1

$105K - $197K/yr

... Associates, Quality Assurance, and Regulatory Affairs to assure compliance with internal and ... Exceptional ability to manage multiple projects in a fast-paced environment with changing ...

Northside Hospital Inc.

Research Associate

Atlanta, GA · On-site

... projects, leveraging data from and generating reports out of research systems and through ... Three (3) to (5) years relevant work experience in a Clinical Research setting. * Knowledge of key ...

Northside Hospital Inc.

Research Associate

Atlanta, GA · On-site

... projects, leveraging data from and generating reports out of research systems and through ... Three (3) to (5) years relevant work experience in a Clinical Research setting. * Knowledge of key ...

Northside Hospital Inc.

Research Associate

Atlanta, GA · On-site

... projects, leveraging data from and generating reports out of research systems and through ... Three (3) to (5) years relevant work experience in a Clinical Research setting. * Knowledge of key ...

Northside Hospital Inc.

Research Associate

Atlanta, GA · On-site

... projects, leveraging data from and generating reports out of research systems and through ... Three (3) to (5) years relevant work experience in a Clinical Research setting. * Knowledge of key ...

Compass Group

PROJECT MANAGER -Hybrid

Sandy Springs, GA · On-site

$100K - $110K/yr

Partner with relevant cross-functional teams (culinary, clinical, EVS, retail and marketing) to set ... At Compass, we are committed to treating all Applicants and Associates fairly based on their ...

Compass Group

PROJECT MANAGER -Hybrid

Sandy Springs, GA · Hybrid

$100K - $110K/yr

Partner with relevant cross-functional teams (culinary, clinical, EVS, retail and marketing) to set ... At Compass, we are committed to treating all Applicants and Associates fairly based on their ...

Compass Group

PROJECT MANAGER -Hybrid

Sandy Springs, GA · Hybrid

$100K - $110K/yr

Partner with relevant cross-functional teams (culinary, clinical, EVS, retail and marketing) to set ... At Compass, we are committed to treating all Applicants and Associates fairly based on their ...

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Clinical Project Associate information

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$10

$26

$46

How much do clinical project associate jobs pay per hour?

As of Sep 13, 2026, the average hourly pay for clinical project associate in Georgia is $26.63, according to ZipRecruiter salary data. Most workers in this role earn between $17.88 and $35.10 per hour, depending on experience, location, and employer.

What is a clinical project associate?

A Clinical Project Associate (CPA) is a professional who supports the planning, execution, and management of clinical trials in the pharmaceutical, biotechnology, or medical device industries. Their responsibilities often include coordinating study documentation, assisting with regulatory submissions, tracking project timelines, and facilitating communication among study teams. CPAs play a crucial role in ensuring that clinical trials are conducted efficiently, ethically, and in compliance with regulatory standards. They work closely with clinical project managers, research associates, and other team members to help bring new therapies and treatments to market.

What are the typical responsibilities of a clinical project associate?

As a Clinical Project Associate, you will play a vital role in ensuring the smooth execution of clinical trials by handling administrative and logistical tasks. Your responsibilities often include maintaining study documentation, coordinating meetings, tracking project timelines, and supporting communication between internal teams and external partners such as clinical sites and vendors. You may also assist with regulatory submissions and help monitor compliance with study protocols. This position offers excellent exposure to the clinical research process and can be a stepping stone to more advanced roles within clinical operations.

What are the key skills and qualifications needed to thrive as a clinical project associate?

To thrive as a Clinical Project Associate, you need a background in life sciences or a related field, attention to detail, and strong organizational skills. Familiarity with clinical trial management systems (CTMS), regulatory documentation, and tools like Microsoft Office is typically required. Excellent communication, teamwork, and time management abilities help professionals excel in supporting project coordination. These skills are crucial for ensuring regulatory compliance, smooth project execution, and effective collaboration within clinical research teams.

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

AspectClinical Project AssociateClinical Research Coordinator
CredentialsBachelor's degree often required; certifications like CCRP beneficialBachelor's degree in health or related field; certifications like CCRP common
Work EnvironmentTypically works with project teams, sponsors, and CROs in clinical trial settingsWorks directly with patients, investigators, and site staff at clinical trial sites
Employer & IndustryPharmaceutical companies, CROs, biotech firmsHospitals, clinics, research sites
Search & Comparison IntentHigh overlap in responsibilities and certificationsSimilar roles but more patient-facing

The Clinical Project Associate primarily supports clinical trial management from a project perspective, working with sponsors and CROs. In contrast, the Clinical Research Coordinator focuses on patient interactions and site management. Both roles require similar educational backgrounds and certifications, but their work environments and daily tasks differ significantly.

What are the most commonly searched types of Clinical Project jobs in Georgia?

The most popular types of Clinical Project jobs in Georgia are:

What are popular job titles related to Clinical Project Associate jobs in Georgia?

For Clinical Project Associate jobs in Georgia, the most frequently searched job titles are:

What job categories do people searching Clinical Project Associate jobs in Georgia look for?

The top searched job categories for Clinical Project Associate jobs in Georgia are:

What cities in Georgia are hiring for Clinical Project Associate jobs?

Cities in Georgia with the most Clinical Project Associate job openings:

Clinical Project Associate jobs near you
Infographic showing various Clinical Project Associate job openings in Georgia as of August 2026, with employment types broken down into 2% As Needed, 78% Full Time, 14% Part Time, and 6% Contract. Highlights an 85% Physical, 1% Hybrid, and 14% Remote job distribution, with an average salary of $55,395 per year, or $26.6 per hour.

Clinical Trials Coordinator

Atlanta, GA • On-site

Children's Healthcare of Atlanta
Hospitals • 10K+ employees
Learn more about Children's Healthcare of Atlantaexternal

$23.75 - $31.75/hr

Full-time

Posted 27 days ago

Key responsibilities

  • Coordinates the care of patients and families enrolled in clinical research trials within accepted practices, policies, and philosophy of Children's Healthcare of Atlanta.

  • Coordinates investigator-initiated and other clinical trials, including communication, regulatory, and research aspects.

  • Develops and oversees the conduct of research protocols, including study design, implementation, data collection, and ensuring reporting requirements are met.

Children's Healthcare Of Atlanta rating

7.5

Company rating: 7.5 out of 10

Based on 130 frontline employees who took The Breakroom Quiz

Job description

Note: If you are CURRENTLY employed at Children's and/or have an active badge or network access, STOP here. Submit your application via Workday using the Career App (Find Jobs).
Work Shift
Day
Work Day(s)
Monday-Friday
Shift Start Time
8:30 AM
Shift End Time
5:00 PM
Worker Sub-Type
Regular
Children's is one of the nation's leading children's hospitals. No matter the role, every member of our team is an essential part of our mission to make kids better today and healthier tomorrow. We're committed to putting you first, and that commitment is at the heart of our company culture: People first. Children always. Find your next career opportunity and make a difference doing what you love at Children's.
Job Description
Coordinates the care of patients and families enrolled in clinical research trials within accepted practices, policies, and philosophy of Children's Healthcare of Atlanta. Coordinates investigator-initiated and other clinical trials, including communication, regulatory, and research aspects. Summarizes study accrual, toxicities, and other data to ensure appropriate documentation onsite and by participating outside institutions. Acts as liaison between the Data and Safety Monitoring Board and Principal Investigators to ensure that studies are regulated and reviewed appropriately for the program. Proactively supports efforts that ensure delivery of safe patient care and services and promote a safe environment at Children's Healthcare of Atlanta.
Experience
  • 3 years of clinical experience with knowledge about the conduct of clinical studies/trials, research principles, and methodologies/study design

Preferred Qualifications
  • Master's degree in Business Administration, Healthcare Administration, or a scientific field
  • Experience in creating and negotiating study budgets and contracts
  • Experience in database development and management
  • Experience managing complex projects

Education
  • Bachelor's degree

Certification Summary
  • Association of Clinical Research Professionals (ACRP), Certified Research Administrator (CRA) or Certified Clinical Research Coordinator (CCRC) or Society of Clinical Research Associates (SOCRA), Certified Clinical Research Professional (CCRP) within 1 year of hire
  • Collaborative Institutional Training Initiative (CITI) within 30 days of employment

Knowledge, Skills, and Abilities
  • Broad knowledge of federal regulations and regulatory requirements for conducting research with the ability to mentor
  • Self-directed and motivated to work independently toward short- and long-term goals
  • Good communication, organization, and interpersonal skills

Job Responsibilities
Develops and oversees conduct of research protocols
  • Assists in the study design and implementation of new studies as requested/needed by the investigator
  • Develops, maintains, utilizes, and updates protocols, data collection tools, case report forms, spreadsheets, and databases for assigned studies.
  • Ensures all reporting requirements are met at participating sites.
  • Confirms patient eligibility from participating sites using eligibility checklists that are created for the project.
  • Conducts site initiation visits (SIV), interim monitoring visits (IMV) and close out visits (COV) for multi-centered studies in compliance with protocol requirements

Provides oversight for data and safety monitoring
  • Maintains the agendas and minutes for the Data and Safety Monitoring Board including scheduling ad hoc meetings.
  • Notifies the Data and Safety Monitoring Board chairperson of unexpected serious adverse drug reactions or serious adverse events.
  • Submission to appropriate regulatory bodies as needed.

Manages regulatory and administrative processes related to clinical research activities for multi-centered trials
  • Develops policies and procedures for the management of multi-centered studies.
  • Completes regulatory site accreditation and audit process of participating sites.
  • Oversees participating institutions to ensure that research and protocol activities comply with organizational guidelines and regulatory standards for multi-centered studies.
  • Serves as a resource for facilitating grants, contracts, and financial tasks for multi-centered clinical research projects.
  • Oversees the maintenance of sites' regulatory binders for purposes of Trial Master File (TMF) documentation.
  • Point of contact for participating sites contracts and payment to sites for study start-up, patient enrollment, and other study needs.
  • Works with study teams and investigators to ensure decisions are being met regarding amendments, dose escalation or de-escalation, suspensions/closures, and notification to regulatory agencies and sponsors.
  • Creates and upkeeps lay and web summaries

Completes data management activities
  • Participates in the development of databases to use as the coordinating center.
  • Develops and communicates project status reports and basic demographic and descriptive statistical information to multi-centered trials.

Performs quality and education activities
  • Provides leadership and training for all multi-centered clinical research activities.
  • Trains participating sites on all activities related to the research project such as eligibility criteria, enrollment instructions, reporting requirements, and monitoring plans including conducting Site initiation visits (SIV) and close out visits (COV).
  • Develops educational in-services for Children's Healthcare of Atlanta staff for assigned studies.

Children's Healthcare of Atlanta is an equal opportunity employer committed to providing equal employment opportunities to all qualified applicants and employees without regard to race, color, sex, religion, national origin, citizenship, age, veteran status, disability or any other characteristic covered by applicable law.
Primary Location Address
1575 Northeast Expy NE
Job Family
Research

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