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Clinical Research Operations Manager Jobs in Georgia

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 ...

New

Clinical Research Nurse

Decatur, GA · On-site

$55 - $75/hr

Operations Employment Type: Full Time Location: Accel Research Sites - Decatur, GA Reporting To ... Under the direction of the Site Manager/Director and the Principal/Sub Investigators, conducts the ...

New

The RA performs clinical, lab, and administrative tasks as needed for the successful operation of ... Under the direction of the Site Manager/Director and the Principal/Sub Investigators, assists the ...

Clinical Research Coordinator The Clinical Research Coordinator will support a post-market ... study operations. * Experience with pre-screening patients and managing patient enrollment ...

Showing results 41-60

Clinical Research Operations Manager information

See Georgia salary details

$29.6K

$82.8K

$157.5K

How much do clinical research operations manager jobs pay per year?

As of Sep 3, 2026, the average yearly pay for clinical research operations manager in Georgia is $82,782.00, according to ZipRecruiter salary data. Most workers in this role earn between $61,200.00 and $95,800.00 per year, depending on experience, location, and employer.

What does a clinical research operations manager do?

A Clinical Research Operations Manager oversees the daily operations of clinical trials to ensure they are conducted efficiently, ethically, and in compliance with regulatory standards. They coordinate between research staff, sponsors, and regulatory bodies, manage budgets and timelines, and ensure proper documentation and reporting. Their role is essential in maintaining the quality and integrity of clinical studies from start to finish.

How does a clinical research operations manager collaborate with cross-functional teams during a study?

As a Clinical Research Operations Manager, you will work closely with cross-functional teams including clinical trial coordinators, data managers, regulatory affairs specialists, and principal investigators. Your role involves facilitating clear communication between departments, ensuring that study milestones are met, and resolving operational issues as they arise. Regular meetings and status updates are common, and you'll often act as a liaison to keep all stakeholders aligned on study objectives, timelines, and compliance requirements. This collaborative approach is crucial for maintaining study integrity and ensuring successful trial outcomes.

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

To thrive as a Clinical Research Operations Manager, you need a solid background in clinical research, regulatory compliance, and project management, often supported by a degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), Good Clinical Practice (GCP) guidelines, and certifications such as ACRP or SOCRA are highly valuable. Leadership, problem-solving, and excellent organizational and communication skills help you manage teams and collaborate effectively with stakeholders. These skills and qualities are crucial for ensuring the successful execution of clinical trials while maintaining regulatory standards and operational efficiency.

What are popular job titles related to Clinical Research Operations Manager jobs in Georgia?

For Clinical Research Operations Manager jobs in Georgia, the most frequently searched job titles are:

What cities in Georgia are hiring for Clinical Research Operations Manager jobs?

Cities in Georgia with the most Clinical Research Operations Manager job openings:

Infographic showing various Clinical Research Operations Manager job openings in Georgia as of August 2026, with employment types broken down into 88% Full Time, 11% Part Time, and 1% Contract. Highlights an 93% Physical, 3% Hybrid, and 4% Remote job distribution, with an average salary of $82,782 per year, or $39.8 per hour.

Clinical Research Coordinator - Oncology Gordon and Redmond

Adventhealth

Gordon, GA • On-site

$42K - $79K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 16 days ago


AdventHealth rating

7.4

Company rating: 7.4 out of 10

Based on 1,279 frontline employees who took The Breakroom Quiz

266th of 898 rated healthcare providers


Job description

Our promise to you:

Joining AdventHealth is about being part of something bigger. It's about belonging to a community that believes in the wholeness of each person, and serves to uplift others in body, mind and spirit. AdventHealth is a place where you can thrive professionally, and grow spiritually, by Extending the Healing Ministry of Christ. Where you will be valued for who you are and the unique experiences you bring to our purpose-minded team. All while understanding that together we are even better.

All the benefits and perks you need for you and your family:

  • Benefits from Day One: Medical, Dental, Vision Insurance, Life Insurance, Disability Insurance

  • Paid Time Off from Day One

  • 403-B Retirement Plan

  • 4 Weeks 100% Paid Parental Leave

  • Career Development

  • Whole Person Well-being Resources

  • Mental Health Resources and Support

  • Pet Benefits

Schedule:

Full time

Shift:

Day (United States of America)

Address:

1035 RED BUD RD NE

City:

CALHOUN

State:

Georgia

Postal Code:

30701

Job Description:

Work Schedule: Monday - Friday, no call no weekends.

  • Manages end-to-end clinical research activities, including patient screening, eligibility, enrollment, and follow-up care.
  • Serves as the primary liaison for participants, investigators, and internal/external research partners.
  • Ensures compliance with clinical research standards, protocols, and AHRI procedures across all patient-facing activities.
  • Coordinates biospecimen collection and maintains HIPAA-compliant databases linking patient data to research samples.
  • Supports research operations through data collection, chart review, and collaboration with clinical, lab, and regulatory teams.

Knowledge, Skills, and Abilities:
Ability to work independently in a fast-paced clinical or research environment, handling multiple tasks simultaneously, effectively, and in an organized and timely manner. [Required]
Knowledge of HIPAA data protection and patient advocacy or similar awareness of ethical treatment of participants in research. [Required]
Ability to communicate effectively with research participants, investigators, research staff, and external partners. [Required]
Ability to apply an analytical approach to problem solving, obtain and analyze facts, and apply sound judgement. [Required]
Ability to accept direction and respond to the changing needs of clinical research units. [Required]
Working knowledge of Microsoft Office applications, such as Word, Excel, Access, Outlook, and Internet knowledge and skills. [Required]
Proficient in the ability to navigate through various electronic data transfer portals and systems. [Required]
Excellent organizational, multi-tasking, and problem-solving skills with extreme attention to detail. [Required]
Strong interpersonal skills to interact and maintain good relationships with a broad spectrum of healthcare disciplines and the public. [Required]
Excellent understanding of project management concepts in order to ensure protocol compliance. [Required]
Specialized knowledge of the unique needs of patients in the assigned therapeutic areas undergoing treatment. [Required]
One to two years skill in human life sciences/biomedical research; physiological, cellular, biochemical, or molecular biology. [Required]
Clinical Trials Management System (or equivalent) and/or Electronic Data Capture (EDC) exposure. [Required]
Advanced computer skills. [Required]
Knowledge of clinical research and research regulatory environment. [Required]
Education:
Bachelors [Required]
Master's [Preferred]
Field of Study:
in a health related
Work Experience:
2+ years of direct clinical research experience or administrative/professional experience working with data or medical information to include duties such as data collection, management and verification [Preferred]
Healthcare experience (medical assistant, allied health care professional, etc.) within an office or hospital setting. [Preferred]
Additional Information:
An equivalent combination of education and relevant work experience may be considered in lieu of the stated degree requirement:

-Bachelor's degree in healthcare or related field AND 0+ research experience OR
-Bachelor's degree in any field AND research experience OR
-Associate's degree in healthcare or related field AND 2+ years of clinical research or healthcare experience OR
-Graduate of an accredited allied health certificate program AND 4+ years of clinical research or healthcare experience
Other certification as applicable to clinical degree or program (i.e., medical assistant, medical technician, phlebotomy) [Preferred]
Licenses and Certifications:
Certified Clinical Research Coordinator (CCRC) [Required]OR Certified Clinical Research Professional (SOCRA) (CCRP) [Required]
Basic Life Support - CPR Cert (BLS) [Preferred]

Pay Range:

$42,839.79 - $79,674.53

This facility is an equal opportunity employer and complies with federal, state and local anti-discrimination laws, regulations and ordinances.


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