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Site Activation Study Jobs in Decatur, GA (NOW HIRING)

IQVIA

Clinical Project Lead, Oncology

Atlanta, GA · Remote

$68K - $232K/yr

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 ...

IQVIA

Clinical Project Lead, Oncology

Atlanta, GA · Remote

$68K - $232K/yr

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 ...

Brasfield & Gorrie, LLC

Energy Marshal

Atlanta, GA

Full-time, project-based, 100% on-site. • Energy Control Plan: Lead and coordinate the site ... activations with MEP subcontractors, commissioning agents, and owner operations teams. • ...

Cleanwater1, Inc

Process Engineer

Norcross, GA · On-site

$75K - $90K/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

... site hypochlorite generation equipment, polymer activation systems, chemical feed systems, air ... Perform time studies, bottleneck analyses, and KPI-based evaluations to drive process improvements ...

Cleanwater1, Inc.

Process Engineer

Norcross, GA · On-site

$75K - $90K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

... site hypochlorite generation equipment, polymer activation systems, chemical feed systems, air ... Perform time studies, bottleneck analyses, and KPI-based evaluations to drive process improvements ...

All JobsSite Activation Study JobsSite Activation Study Jobs in Decatur, GA

Site Activation Study information

See Decatur, GA salary details

$9

$17

$22

How much do site activation study jobs pay per hour?

As of Aug 16, 2026, the average hourly pay for site activation study in Decatur, GA is $17.46, according to ZipRecruiter salary data. Most workers in this role earn between $15.96 and $18.80 per hour, depending on experience, location, and employer.

What is a site activation study?

Site Activation Study professionals are responsible for overseeing and managing the process of initiating clinical trial sites. Their main tasks include coordinating regulatory document collection, ensuring sites comply with study protocols, and facilitating the start-up activities necessary for clinical trials. They work closely with investigators, site staff, and sponsors to guarantee that all requirements are met for a trial to begin at each site. Their role is crucial for ensuring timely and efficient study launches while maintaining regulatory compliance.

What are common challenges faced in site activation study roles, and how can they be overcome?

Professionals in Site Activation Study roles often encounter challenges such as tight timelines for site initiation, navigating varying regulatory requirements across regions, and coordinating with multiple stakeholders. Successfully overcoming these challenges requires strong organizational skills, clear communication, and a proactive approach to problem-solving. Building collaborative relationships with clinical sites and staying updated on regulatory changes can also help streamline activation processes and minimize delays.

What are the key skills and qualifications needed for site activation study roles?

To thrive in a Site Activation Study role, you need a solid understanding of clinical research processes, regulatory requirements, and project management, typically supported by a degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), regulatory submission platforms, and Good Clinical Practice (GCP) certification is often required. Strong attention to detail, excellent organizational skills, and effective communication abilities are vital for coordinating with multiple stakeholders and ensuring timely site activation. These skills and qualifications are essential to efficiently navigate complex regulatory environments and to ensure clinical trials start on schedule.

What is the difference between Site Activation Study vs Site Coordinator?

AspectSite Activation StudySite Coordinator
Primary RolePlanning and overseeing the setup of clinical trial sitesManaging daily site operations and participant coordination
Required CredentialsClinical research experience, sometimes certificationsExperience in clinical settings, organizational skills
Work EnvironmentResearch sites, clinical trial settingsClinical sites, hospitals, research facilities
Industry UsageUsed during trial startup phaseOngoing site management during trials

While both roles are involved in clinical trials, the Site Activation Study focuses on preparing and initiating trial sites, whereas the Site Coordinator manages daily operations once the site is active. Understanding these differences helps in selecting the right role for your career or hiring needs.

What job categories do people searching Site Activation Study jobs in Decatur, GA look for?

The top searched job categories for Site Activation Study jobs in Decatur, GA are:

What cities near Decatur, GA are hiring for Site Activation Study jobs?

Cities near Decatur, GA with the most Site Activation Study job openings:

Site Activation Study jobs near you

Clinical Research Manager (68740)

ATLANTA GASTRO

Atlanta, GA • On-site

Full-time

Posted 8 days ago

Job description

GENERAL SUMMARY OF DUTIES: Leads day-to-day multi-site clinical research operations, staff, and study execution from feasibility through closeout in alignment with the Director's strategy.
Exceptional candidates with experience beyond the posted level are encouraged to apply. Based on qualifications, experience, and organizational needs, consideration may be given to placement at a higher level.
RESPONSIBILITIES:
Duties include but are not limited to:
  • Supervise and provide leadership to Clinical Research Coordinators and Research Assistants/Interns
  • Lead day-to-day multi-site clinical research operations and promote consistent, efficient study execution
  • Manage the study lifecycle from feasibility and startup through conduct, monitoring, and closeout
  • Track enrollment, timelines, milestones, compliance, and data quality; resolve issues and escalate significant risks
  • Serve as the operational liaison among investigators, sponsors, CROs, vendors, staff, and centralized support teams
  • Ensure regulatory documentation and study activities meet FDA, ICH-GCP, HIPAA, IRB, sponsor, and organizational requirements
  • Conduct quality reviews, implement SOPs and CAPAs, and maintain audit and inspection readiness
  • Recruit, onboard, train, mentor, evaluate, and allocate research staff based on study and site priorities
  • Support research systems, standardized workflows, and practical process improvements across sites

EDUCATION, SKILLS, & EXPERIENCE:
  • Required:
    • Bachelor's degree in nursing, life sciences, public health, healthcare administration, or a related field
    • At least five years of clinical research experience, including study coordination or site management and direct supervision of research personnel.
    • Demonstrated experience managing study startup, site activation, conduct, monitoring, closeout, and multi-site operational workflows
    • Knowledge of FDA regulations, ICH-GCP, HIPAA, and IRB requirements, with strong project management, people-leadership, communication, and organizational skills
  • Preferred:
    • Master's degree in clinical research, healthcare administration, public health, nursing, or a related field
    • Clinical research certification and experience with research systems and process improvement

WORK ENVIRONMENT:
Requires sitting and standing associated with a normal office environment. Travel required as business needs dictate.
DRUG FREE WORKPLACE:
United Digestive is a drug-free workplace. All offers of employment are contingent upon passing a pre-employment drug screening.
EQUAL OPPORTUNITY EMPLOYER:
United Digestive is an equal opportunity employer and will not tolerate discrimination in employment on the basis of race, color, age, sex, sexual orientation, gender identity or expression, religion, disability, ethnicity, national origin, marital status, veteran status, genetic information or any other legally protected classification or status.
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