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Clinical Trial Manager Jobs in Decatur, GA (NOW HIRING)

Incredible Health

Nurse Manager - Oncology

Marietta, GA · On-site

$59K - $100K/yr

Assistant Nurse Manager, BMT, CNO, Charge, Chemo or oncology certified, Chemotherapy/Biotherapy provider card, Chemotherapy/Immunotherapy certification, Clinical Nurse Coordinator, Clinical trial ...

Incredible Health

Nurse Manager - Oncology

Marietta, GA · On-site

$59K - $100K/yr

Assistant Nurse Manager, BMT, CNO, Charge, Chemo or oncology certified, Chemotherapy/Biotherapy provider card, Chemotherapy/Immunotherapy certification, Clinical Nurse Coordinator, Clinical trial ...

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Clinical Trial Manager information

See Decatur, GA salary details

$28

$61

$93

How much do clinical trial manager jobs pay per hour?

As of Aug 20, 2026, the average hourly pay for clinical trial manager in Decatur, GA is $61.04, according to ZipRecruiter salary data. Most workers in this role earn between $49.52 and $68.75 per hour, depending on experience, location, and employer.

What does a clinical trial manager do?

A clinical trial manager, or CTM, oversees research and each phase of clinical drug tests at a hospital. They work closely with both the doctors and clinicians who are performing the trial, as well as the sponsor of the study, which is typically a pharmaceutical company or other health care organization. As a CTM, duties and responsibilities include planning and managing the trial, making sure that the test meets all government standards, and determining if it was successful. Clinical trial managers also hire, train, and evaluate the members of the clinical team.

What does a clinical trial manager do?

A Clinical Trial Manager oversees the planning, coordination, and execution of clinical trials for new drugs, medical devices, or treatments. They ensure that trials are conducted in compliance with regulatory guidelines, company protocols, and ethical standards. Their responsibilities include managing budgets, timelines, and teams, as well as monitoring data quality and safety throughout the study. Clinical Trial Managers also work closely with investigators, sponsors, and regulatory agencies to ensure successful trial outcomes.

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

To thrive as a Clinical Trial Manager, you need a solid background in life sciences, clinical research experience, and often a relevant bachelor's or master's degree. Familiarity with clinical trial management systems (CTMS), regulatory requirements like GCP, and certifications such as ACRP or SOCRA are highly beneficial. Strong organizational skills, attention to detail, leadership, and effective communication are critical soft skills for managing teams and stakeholders. These skills ensure trials are conducted ethically, efficiently, and compliantly, leading to successful study outcomes.

What are some common challenges clinical trial managers face when coordinating multi-site studies?

Clinical Trial Managers often encounter challenges such as ensuring consistent protocol implementation across different sites, managing timelines in the face of site-specific delays, and maintaining clear communication among diverse teams. They must also navigate regulatory differences between regions and address unforeseen issues like patient recruitment shortfalls or data discrepancies. Success in this role requires strong organizational skills, adaptability, and proactive problem-solving to keep studies on track and compliant.

How much does a clinical trial manager earn?

A clinical trial manager's salary varies based on experience, location, and the size of the organization, but typically ranges from $80,000 to $130,000 annually. Senior managers or those with specialized skills and certifications can earn higher salaries, often exceeding $150,000. The role often requires knowledge of regulatory requirements and project management tools.

What qualifications do you need to be a clinical trial manager?

A clinical trial manager typically needs a bachelor's degree in life sciences, healthcare, or a related field, along with experience in clinical research or project management. Many roles also require knowledge of Good Clinical Practice (GCP) guidelines and proficiency with trial management software. Advanced degrees or certifications such as the Certified Clinical Research Professional (CCRP) can enhance job prospects.
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What cities near Decatur, GA are hiring for Clinical Trial Manager jobs?

Cities near Decatur, GA with the most Clinical Trial Manager job openings:

Clinical Trial Manager jobs near you
Infographic showing various Clinical Trial Manager job openings in Decatur, GA as of August 2026, with employment types broken down into 84% Full Time, 15% Part Time, and 1% Contract. Highlights an 81% Physical, 2% Hybrid, and 17% Remote job distribution, with an average salary of $126,957 per year, or $61 per hour.

Manager- Clinical Research Operations

Northside Hospital Inc.

Atlanta, GA • On-site

Full-time

Re-posted 13 days ago

Northside Hospital rating

7.3

Company rating: 7.3 out of 10

Based on 443 frontline employees who took The Breakroom Quiz

306th of 889 rated healthcare providers

Job description

Overview

Northside Hospital is award-winning, state-of-the-art, and continually growing. Constantly expanding the quality and reach of our care to our patients and communities creates even more opportunity for the best healthcare professionals in Atlanta and beyond. Discover all the possibilities of a career at Northside today.

Responsibilities

PRIMARY DUTIES AND RESPONSIBILITIES

  • Manage research projects assigned by the Research Program Director
  • Manage assigned departments/staff
  • Support Research Program with the development of appropriate goals, metrics and required documentation of project activities.
  • Identify collaborative opportunities across project teams, practices, and hospital departments.
  • Coordinate and lead meetings with NSH departments analyzing the feasibility of new research projects.
  • Ensure the quality and integrity of research.
  • Serve as a point of contact for Monitor visits from CROs, SMOs, and sponsors to help coordinate the visits with CRCs and CRNs and the availability of all necessary information to ensure accuracy and compliance.
  • Monitors all research activity and maintains awareness of all clinical research projects.
  • Provides compliance oversight for day-to-day operations
  • Develops, maintains, and evaluates the SOPs for administering clinical research
  • Conducts training on GCP, FDA, NIH, Human Subject Protection and necessary regulations. 
    • ADDITIONAL DUTIES AND RESPONSIBILITIES
  • Resolve research conflicts during the normal course of business
  • Maintain professional knowledge and skills, particularly in the areas of Good Clinical Practice guidelines and other research regulations
  • Participate in the review, development and maintenance of automated processes and information technology for clinical research related activities
  • Develop, maintain, and deliver education and training programs for the NSH research community, protection of human subjects, the research life cycle, protocol development, monitoring visits, and others.
  • Other duties as assigned
    • Qualifications

    KNOWLEDGE SKILLS AND ABILITIES/LICENSE OR CERTIFICATION REQUIRED

  • Bachelor's degree in a relevant field.  MBA preferred.
  • Minimum of 5 years' experience in a clinical research setting
  • Ability to correctly interpret laws, regulations and policies related to research compliance
  • Excellent organizational and project management skills with the ability to manage multiple tasks simultaneously
  • Knowledge of clinical trial policies and regulations and Good Clinical Practice (GCP)
  • Established interpersonal skills combined with the ability to be highly motivated and work independently
  • Demonstrated analytical and problem solving skills
  • Ability to work independently and as part of a team
  • Ability to manage teams of varying sizes
  • Knowledge of information technology systems supporting regulatory affairs, IRB and compliance research administration

    • KNOWLEDGE SKILLS AND ABILITIES/LICENSE OR CERTIFICATION PREFERRED

  • Certification relative to the position
    • Work Hours:8:00AM-5:00PMWeekend Requirements:NoOn-Call Requirements:NoEmployment Type: FULL_TIME

    What Northside Hospital employees say

    Pay

    Benefits

    Hours and flexibility

    Workplace

    Get the full story on Breakroom

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    About Northside Hospital

    Sourced by ZipRecruiter

    * 288-bed hospital, offering a full range of services including comprehensive and interventional stroke care, preventative and corrective cardiac care, full-service orthopedic and spine treatment, an ER 24/7®, and general surgery * As one of the first hospitals in the area to achieve Atrial Fibrillation Certification (SCPC), our technologically advanced hospital allows our highly skilled physicians, nursing and caregivers to serve our growing community * Northside Hospital was the first nationally recognized Comprehensive Stroke Center in Pinellas County and nationally recognized for quality and safety by earning an 'A' rating from the Leapfrog Group

    Industry

    Hospitals

    Company size

    10,000+ Employees

    Headquarters location

    Atlanta, GA, US

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