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Ctm Jobs in Georgia (NOW HIRING)

Coca-Cola

Senior Director, Trade Finance

Atlanta, GA · On-site

Maintain financial controls and financial reporting for CTM (Cooperative Trade Marketing), GTM (Go To Market Funds), and SMF (Special Marketing Funds). * Responsible for the global key customer ...

Burger King

District Manager of Burger King

Atlanta, GA · On-site

$70K - $75K/yr

High school diploma or equivalent and demonstrated 1+ years "above store" restaurant management in operations -or- 2+ years' experience as CTM and 2+ years' experience in restaurant operations as ...

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$24

$52

$81

How much do ctm jobs pay per hour?

As of Aug 23, 2026, the average hourly pay for ctm in Georgia is $52.79, according to ZipRecruiter salary data. Most workers in this role earn between $42.84 and $59.47 per hour, depending on experience, location, and employer.

What is a Clinical Trial Manager?

Clinical Trial Managers (CTMs) are professionals responsible for overseeing and coordinating the planning, implementation, and management of clinical trials. They ensure that trials are conducted according to regulatory guidelines, study protocols, and timelines, while maintaining high standards for patient safety and data integrity. CTMs manage teams, budgets, site selection, and communications between sponsors, investigators, and regulatory bodies throughout the course of a clinical study.

What are some common challenges faced by Clinical Trial Managers when overseeing multi-site studies, and how can these be addressed?

Clinical Trial Managers often encounter challenges such as maintaining consistent communication across multiple sites, ensuring protocol adherence, and managing timelines. These challenges can be addressed by establishing clear lines of communication, utilizing centralized project management tools, and holding regular meetings with site coordinators. Developing strong relationships with site staff and proactively identifying potential issues can also help CTMs keep studies on track and maintain data quality.

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 strong background in life sciences or a related field, extensive knowledge of clinical trial processes, and experience with regulatory compliance, often supported by a relevant degree. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and certifications like GCP (Good Clinical Practice) are typically required. Excellent organizational, leadership, and communication skills are vital for effectively managing teams and collaborating with stakeholders. These skills and qualifications ensure the successful planning, execution, and oversight of clinical trials while maintaining regulatory standards and patient safety.

What is the difference between Ctm vs Construction Project Coordinator?

AspectCtmConstruction Project Coordinator
Required CredentialsTypically requires certifications like OSHA, OSHA 30-hour, or specific trade licensesOften requires certifications such as OSHA, PMP, or related project management credentials
Work EnvironmentOn-site construction sites, industrial settings, or manufacturing facilitiesConstruction sites, offices, and project management offices
Employer & Industry UsageUsed mainly in manufacturing, industrial, or construction sectorsCommonly employed in construction firms, engineering companies, and project management firms

The main difference between a Ctm and a Construction Project Coordinator lies in their focus areas. Ctm roles often emphasize technical and safety certifications within industrial or manufacturing environments, while Construction Project Coordinators focus on managing project timelines, budgets, and coordination within construction projects. Both roles require safety knowledge and some project management skills, but their day-to-day responsibilities and industry contexts differ.

How much does a CTM make?

A CTM (Clinical Trial Manager) typically earns between $80,000 and $130,000 annually, depending on experience, location, and the size of the organization. They oversee clinical trial operations, requiring strong project management skills and knowledge of regulatory requirements.

How to become a CTM?

To become a CTM (Certified Transportation Manager) or similar role, candidates typically need relevant experience in transportation or logistics, often requiring a background in supply chain management. Earning industry certifications such as the Certified Transportation Manager (CTM) credential and developing skills in operations, compliance, and safety are important steps. A bachelor's degree in logistics, business, or a related field can also enhance prospects.

What are popular job titles related to Ctm jobs in Georgia?

For Ctm jobs in Georgia, the most frequently searched job titles are:

What job categories do people searching Ctm jobs in Georgia look for?

The top searched job categories for Ctm jobs in Georgia are:

Ctm jobs near you
Infographic showing various Ctm job openings in Georgia as of August 2026, with employment types broken down into 87% Full Time, 6% Part Time, and 7% Contract. Highlights an 72% Physical, 5% Hybrid, and 23% Remote job distribution, with an average salary of $109,799 per year, or $52.8 per hour.

Clinical Research Coordinator

ClinLab Solutions Group

Savannah, GA • On-site

$22.50 - $30/hr

Other

Posted 3 days ago

New

Job description

Essential Responsibilities and Duties:

  • Coordinates patient-related activities for complex and/or multiple studies under supervision, from study startup through close-out.
  • Maintains and organizes clinical trial research documentation.
  • Monitors study subjects and supports data analysis and reporting.
  • Coordinates the timing and collection of study data.
  • Identifies, documents, and reports adverse events, protocol deviations, and other unanticipated problems through the appropriate channels.
  • Tracks and reports research data to uphold quality and regulatory compliance.
  • Completes study-related administrative and regulatory tasks as needed.
  • Contributes to protocol development activities.
  • Confirms the site receives accurate information and materials from sponsors (e.g., source documents, protocol, scales, supplies, approvals, contacts).
  • Explains protocol-specific requirements and expectations to prospective participants and their caregivers.
  • Conducts protocol-required safety and efficacy assessments (vital signs, EKGs, blood draws, and other assigned procedures).
  • Supports the Clinical Trial Manager (CTM) in overseeing vendors, accounting, regulatory matters, client satisfaction, recruitment, quality, and trial outcomes.
  • Assists the CTM with planning, process development, staff training, and team development.
  • Takes on additional duties as assigned. The responsibilities above describe the general level and nature of work for this role and are not intended to be all-inclusive.


Education / Experience / Skills:

  • Proven experience and demonstrated proficiency as a Clinical Research Coordinator.
  • High school diploma or equivalent required; Bachelor's degree preferred.
  • CCRC certification preferred.
  • 2–3 years of experience in the medical field preferred.
  • Working knowledge of federal regulations governing the protection of human research subjects and the conduct of clinical trials.
  • Strong leadership and mentorship abilities.
  • Skilled at building and maintaining effective working relationships across all levels of the organization, as well as with sponsors and vendors.
  • Sound crisis management and problem-solving skills, with the ability to stay calm and effective under pressure.
  • Works well both independently and as part of a team.
  • Strong verbal and written communication skills.


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