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Ctms Jobs in Georgia (NOW HIRING)

IQVIA

Clinical Project Lead, Oncology

Atlanta, GA · Remote

$68K - $232K/yr

Ensure inspection readiness through complete and accurate trial documentation (CTMS, eTMF) * Oversee patient safety reporting (AEs/SAEs) within required timelines Financial & Vendor Management

IQVIA

Clinical Project Lead, Oncology

Atlanta, GA · Remote

$68K - $232K/yr

Ensure inspection readiness through complete and accurate trial documentation (CTMS, eTMF) * Oversee patient safety reporting (AEs/SAEs) within required timelines Financial & Vendor Management

Zimmer Biomet

$13.50 - $18/hr

... CTMS). How You'll Create Impact * Assist in testing and maintaining clinical software applications under the guidance of experienced developers and analysts. * Support the documentation of technical ...

Zimmer Biomet

$14 - $18.50/hr

... CTMS). How You'll Create Impact * Assist in testing and maintaining clinical software applications under the guidance of experienced developers and analysts. * Support the documentation of technical ...

Zimmer Biomet

2025 Fall Intern, Clinical Applications

Athens, GA · On-site

$12.50 - $16.75/hr

... CTMS). How You'll Create Impact * Assist in testing and maintaining clinical software applications under the guidance of experienced developers and analysts. * Support the documentation of technical ...

Zimmer Biomet

$13.75 - $18.25/hr

... CTMS). How You'll Create Impact * Assist in testing and maintaining clinical software applications under the guidance of experienced developers and analysts. * Support the documentation of technical ...

Zimmer Biomet

$13.75 - $18.50/hr

... CTMS). How You'll Create Impact * Assist in testing and maintaining clinical software applications under the guidance of experienced developers and analysts. * Support the documentation of technical ...

Zimmer Biomet

2025 Fall Intern, Clinical Applications

Macon, GA · On-site

$14.50 - $19.25/hr

... CTMS). How You'll Create Impact * Assist in testing and maintaining clinical software applications under the guidance of experienced developers and analysts. * Support the documentation of technical ...

Centricity Research

Clinical Screening Coordinator

Rincon, GA · On-site

$22 - $29.25/hr

Feel confident using everyday computer tools like spreadsheets, databases, and email, and are open to learning systems like CTMS or EMR * Bring experience from a healthcare, research, or customer ...

Javara Inc.

Clinical Trial Navigator I

Thomasville, GA · On-site

Ensure scientific integrity of data and record source data appropriately and accurately inclusive of patient visit data within source, CTMS, electronic reporting systems, completing the sponsor ...

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Ctms information

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How much do ctms jobs pay per hour?

As of Aug 18, 2026, the average hourly pay for ctms in Georgia is $12.33, according to ZipRecruiter salary data. Most workers in this role earn between $12.16 and $12.79 per hour, depending on experience, location, and employer.

What is a CTMS?

A CTMS (Clinical Trial Management System) job typically involves managing and maintaining software used to track clinical trials. Professionals in this role ensure that study data, timelines, budgets, and regulatory compliance are properly documented and maintained. They may work in pharmaceutical companies, contract research organizations (CROs), or healthcare institutions, collaborating with clinical teams to streamline trial operations. The role often requires knowledge of clinical trial processes, data management, and regulatory requirements.

What are the typical responsibilities of someone working in a CTMS-related role?

Professionals working with Clinical Trial Management Systems are responsible for maintaining and updating study data, overseeing trial documentation, and ensuring alignment with regulatory requirements. They often coordinate with clinical research teams, data managers, and regulatory authorities to secure timely and accurate trial progress. Common challenges include balancing multiple studies simultaneously and ensuring data integrity across all phases. The role offers opportunities to develop expertise in clinical operations and can be a strong stepping stone toward advanced positions in clinical project management. Daily responsibilities often involve system troubleshooting, user support, and facilitating communication between different departments.

What are the key skills and qualifications needed to thrive in the CTMS position, and why are they important?

To thrive in a CTMS (Clinical Trial Management System) role, you need a solid understanding of clinical research processes, data management, and regulatory compliance, generally supported by a degree in life sciences or related fields. Proficiency with CTMS software such as Medidata, Oracle Siebel, or Veeva Vault, along with familiarity with GCP (Good Clinical Practice) guidelines, is essential. Excellent organizational skills, attention to detail, and strong communication abilities distinguish outstanding candidates in this position. These skills ensure accurate trial documentation, streamlined workflows, and regulatory compliance in the complex field of clinical research.

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

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

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

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

What cities in Georgia are hiring for Ctms jobs?

Cities in Georgia with the most Ctms job openings:

Ctms jobs near you
Infographic showing various Ctms job openings in Georgia as of August 2026, with employment types broken down into 89% Full Time, 4% Part Time, and 7% Contract. Highlights an 74% Physical, 4% Hybrid, and 22% Remote job distribution, with an average salary of $25,645 per year, or $12.3 per hour.

Clinical Project Lead, Oncology

IQVIA

Atlanta, GA • Remote

$68K - $232K/yr

Full-time

Re-posted 22 days ago

IQVIA rating

8.1

Company rating: 8.1 out of 10

Based on 53 frontline employees who took The Breakroom Quiz

62nd of 224 rated it services

Job description

In this remote role you will serve as the primary country-level leader for clinical trial delivery, ensuring studies are executed efficiently from start-up through closeout. You will oversee local trial operations, drive performance, and collaborate cross-functionally to deliver high-quality data aligned with regulatory requirements and sponsor expectations.

This role is ideal for a clinical operations professional who thrives in a fast-paced, large matrixed environment and is passionate about improving patient outcomes through clinical research.

Key Responsibilities

Clinical Trial Delivery & Oversight

  • Lead end-to-end country-level trial management, from study start-up through database lock and closeout
  • Serve as the primary contact for assigned clinical trials within your country
  • Ensure delivery of high-quality, compliant data and documentation aligned with ICH-GCP, SOPs, and regulatory standards
  • Contribute to site level recruitment strategy and contingency planning and implementation in partnership with other functional areas to achieve clinical research target

Site & Stakeholder Management

  • Partner with CRA's, Global Project Leads, and cross-functional teams to ensure successful study execution
  • Lead site feasibility, selection, and activation processes
  • Drive investigator engagement and site performance, including recruitment and retention strategies

Operational Excellence & Compliance

  • Monitor study progress through systems and reports; implement corrective and preventive actions (CAPA) when needed
  • Ensure inspection readiness through complete and accurate trial documentation (CTMS, eTMF)
  • Oversee patient safety reporting (AEs/SAEs) within required timelines

Financial & Vendor Management

  • Manage country-level budgets, forecasting, and financial tracking
  • Oversee local vendors and site payments, ensuring timely and accurate processing

Regulatory & Quality Assurance

  • Coordinate ethics and regulatory submissions/approvals in collaboration with start-up teams
  • Ensure compliance with local regulations and global standards (ICH-GCP)

What You Bring

Required Qualifications

  • Bachelor's degree in life sciences, healthcare, or related field
  • Strong knowledge of ICH-GCP, regulatory requirements, and clinical trial processes
  • Excellent communication and stakeholder management skills
  • Proficiency in clinical systems (e.g., CTMS, eTMF)
  • 3-5+ years of total trial management experience
  • Experience managing complex or early-phase trials
  • Demonstrated ability to lead cross-functional teams and drive performance

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more athttps://jobs.iqvia.com

IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

The potential base pay range for this role, when annualized, is $68,400.00 - $232,800.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

What IQVIA employees say

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Benefits

Hours and flexibility

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About IQVIA

Sourced by ZipRecruiter

At IQVIA, we are passionate about helping customers and partners improve results and patient outcomes. Everything we do contributes to this vision for creating a healthier world. In today’s healthcare environment, it’s not only about how much data, information, and technology you have at your fingertips – it’s what you do with it. IQVIA is focused on making intelligent connections for customers across the entire healthcare ecosystem to help you drive healthcare forward. Whether that means partnering with novel technology companies to boost patient engagement, leveraging AI & machine learning to accelerate results, or using decentralized trials to reach the right patients wherever they are – we are always looking for smarter ways to move you forward.

Industry

Health care and social assistance

Company size

10,000+ Employees

Headquarters location

Durham, NC, US

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