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Clinical Trial Jobs in Decatur, GA (NOW HIRING)

IQVIA

Clinical Project Lead, Oncology

Atlanta, GA · Remote

$68K - $232K/yr

You will oversee local trial operations, drive performance, and collaborate cross-functionally to ... This role is ideal for a clinical operations professional who thrives in a fast-paced, large ...

IQVIA

Clinical Project Lead, Oncology

Atlanta, GA · Remote

$68K - $232K/yr

You will oversee local trial operations, drive performance, and collaborate cross-functionally to ... This role is ideal for a clinical operations professional who thrives in a fast-paced, large ...

ICON

Clinical Research Associate

Atlanta, GA · On-site +1

You will contribute to clinical trial monitoring activities, taking responsibility for your deliverables and working collaboratively. Key responsibilities include: * Conducting site qualification ...

VIVEX BIOLOGICS INC

Clinical Project Manager

Atlanta, GA · On-site

... trial designs and endpoints. · Prepares and presents findings of assigned studies to internal and external stakeholders. · Leads and manages the execution of assigned clinical studies. · Oversees ...

CenExel

Clinical Research Coordinator

Decatur, GA · On-site

$23.75 - $31.50/hr

Our world-class PIs, advanced patient engagement strategies, premium data analytics, and integrated operations optimize every step of the clinical trial process. Along with an exceptional work ...

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All JobsClinical Trial JobsClinical Trial Jobs in Decatur, GA

Clinical Trial information

See Decatur, GA salary details

$28

$61

$93

How much do clinical trial jobs pay per hour?

As of Jun 20, 2026, the average hourly pay for clinical trial 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 qualifications do you need to work in clinical trials?

To work in clinical trials, candidates typically need a relevant educational background such as a bachelor's degree in health sciences, biology, or a related field. Additional qualifications may include experience with Good Clinical Practice (GCP) guidelines, strong organizational skills, and sometimes certifications like Certified Clinical Research Professional (CCRP). Specific roles may require advanced degrees or specialized training depending on responsibilities.

What are clinical trials?

Clinical trials are research studies that involve human participants and are designed to evaluate the safety and effectiveness of new medical treatments, drugs, or devices. These trials follow a carefully controlled protocol and are conducted in phases to systematically assess outcomes. Participants may include patients with specific medical conditions or healthy volunteers, depending on the study's goals. The results from clinical trials help inform medical decisions and regulatory approvals for new therapies.

What are the key skills and qualifications needed to thrive in a Clinical Trial role, and why are they important?

To thrive in a Clinical Trial role, you need a solid understanding of clinical research principles, regulatory compliance, and data management, usually supported by a degree in life sciences or a related field. Familiarity with electronic data capture (EDC) systems, Good Clinical Practice (GCP) certification, and clinical trial management software is typically required. Strong attention to detail, organizational abilities, and effective communication skills help professionals coordinate complex processes and collaborate with interdisciplinary teams. These competencies are vital to ensure trials are conducted ethically, efficiently, and in compliance with regulatory standards.

What job makes $10,000 a month without a degree?

In the field of clinical trials, roles such as clinical research coordinators or project managers can earn around $10,000 per month with extensive experience and specialized skills, often without requiring a traditional degree but sometimes needing certifications. These positions typically involve managing trial processes, ensuring compliance, and coordinating between teams, often requiring knowledge of regulatory standards and trial protocols.

What are some common challenges faced by professionals working in clinical trial management, and how can they be addressed?

Professionals in clinical trial management often encounter challenges such as adhering to strict regulatory requirements, managing complex timelines, and ensuring effective communication among multidisciplinary teams. Overcoming these challenges typically involves thorough planning, continuous training on regulatory updates, and the use of project management tools to track progress and coordinate tasks. Building strong relationships with investigators and fostering open communication can also help address issues quickly and maintain trial integrity.

How much money can I make doing clinical trials?

Clinical trial participants can earn anywhere from $50 to $500 per visit, depending on the study's complexity, duration, and location. Compensation varies based on factors such as the type of trial, required procedures, and whether the participant is a healthy volunteer or has a specific condition. Participants often need to meet certain health criteria and may undergo medical assessments before enrollment.

What jobs pay 2000 a day?

In the context of clinical trials, highly specialized roles such as principal investigators, clinical trial consultants, or senior contract research organization (CRO) executives can earn around $2,000 per day, especially for large or complex studies. These positions typically require extensive experience, advanced degrees, and often involve managing trial operations, data analysis, or regulatory compliance.
What are the most commonly searched types of Clinical Trial jobs in Decatur, GA? The most popular types of Clinical Trial jobs in Decatur, GA are:
What are popular job titles related to Clinical Trial jobs in Decatur, GA? For Clinical Trial jobs in Decatur, GA, the most frequently searched job titles are:
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What cities near Decatur, GA are hiring for Clinical Trial jobs? Cities near Decatur, GA with the most Clinical Trial job openings:
Clinical Trial jobs near you
Clinical Trial Assistant

Clinical Trial Assistant

VIVEX BIOLOGICS INC

Atlanta, GA • On-site

Full-time

Posted 10 days ago

Job description

Description:

Job purpose

The Clinical Trial Assistant will provide administrative support to the Clinical team. Responsible for assisting with day-to-day operations of clinical studies. This position requires basic knowledge of clinical trials, excellent organizational skills and the ability to perform at high levels in a fast-paced, dynamic environment.

Duties and responsibilities

  1. Assist team members with designated administrative tasks in support of clinical trial execution and management.
  2. Perform study tracking to ensure that study files are current, accurate and complete with applicable local regulatory requirements and ICH/GCP guidelines.
  3. Assist in generation of study start up materials and support feasibility study activities.
  4. Participate in the design and implementation of case report forms (CRF) and completion guidelines, and database testing.
  5. Maintain clinical study schedules; collaborate with study team on subject tracking to ensure protocol compliance.
  6. Maintain and organize publication library, clinical study documents and reference materials.
  7. Assist Clinical Research Associates (CRA) and management with resolution of issues
  8. Able to review data within the Electronic Data Capture (EDC) and file management systems, perform and collate data downloads, reports, and prepare summaries of data extractions for review.
  9. Collaborate with CRAs, Data Management and vendors on data cleaning, tracking and data analysis quality.
  10. Assist in the production of presentations, etc., as needed for project, departmental, and/or business development presentations.
  11. Actively order and maintain ancillary clinical study supplies required for conduct of clinical trials.
  12. Assist with preparation, shipping, handling, distribution, and/or accountability of clinical trial supplies.
  13. Contribute to the development of clinical trial management best practice processes and Standard Operating Procedures (SOP).
  14. Maintain up-to-date knowledge of current regulations and guidelines to ensure compliance.
  15. Solve routine problems of limited scope and complexity following established policies and procedures.
  16. Work collaboratively with team to solve more complex issues.
  17. Other duties as assigned.


Requirements:

Skills

  1. Proficient in Microsoft Office applications (Word, Excel, and PowerPoint), Adobe and video/web conferencing. Knowledge of relational databases.
  2. Basic knowledge of clinical regulations and guidance including GCPs, and ICH guidelines.
  3. Excellent organizational skills, ability to manage multiple tasks and meticulous attention to detail.

Qualifications

Bachelor’s degree or equivalent and related work experience preferred. Excellent communication, teamwork, organizational, interpersonal, and problem-solving skills.

Working conditions

Office Environment, Laboratory Environment.

May be required to travel up to 15% of the time

Physical requirements

While performing the duties of this job, the employee is regularly required to sit for prolonged periods of time.

The employee may occasionally be required to pull, lift and/or move up to 20 pounds.

Direct reports

Nothing in this job description restricts management’s right to assign or reassign duties and responsibilities to this job any time.