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

START Research

Director, Study Operations

Atlanta, GA · On-site

$150 - $200/hr

We areseekingaDirector of Study Operations.This role will lead research operations, ensuring all ... Intermittent travel, less than quarterly, to support new site activation Best-in-Class Benefits and ...

Alcanza

Clinical Site Director

Decatur, GA · On-site

$78K - $106K/yr

... study milestones (such as site activation targets, enrollment targets, etc.), meet budgets, and delivery quality data to sponsors. * Reviewing the performance dashboards and other clinical trial ...

Alcanza Clinical Research

Clinical Site Director

Decatur, GA · On-site

$78K - $106K/yr

... study milestones (such as site activation targets, enrollment targets, etc.), meet budgets, and delivery quality data to sponsors. * Reviewing the performance dashboards and other clinical trial ...

Alcanza Clinical Research

Clinical Site Director

Decatur, GA · On-site

$87K - $119K/yr

... study milestones (such as site activation targets, enrollment targets, etc.), meet budgets, and delivery quality data to sponsors. * Reviewing the performance dashboards and other clinical trial ...

Accel Research Sites

Clinical Site Director

Decatur, GA · On-site

$150 - $200/hr

... study milestones (such as site activation targets, enrollment targets, etc.), meet budgets, and delivery quality data to sponsors. * Reviewing the performance dashboards and other clinical trial ...

United-Digestive

Clinical Research Manager

Atlanta, GA · On-site

$100 - $125/hr

Demonstrated experience managing study startup, site activation, conduct, monitoring, closeout, and multi-site operational workflowsKnowledge of FDA regulations, ICH-GCP, HIPAA, and IRB requirements ...

Brasfield & Gorrie, LLC

Energy Marshal

Atlanta, GA · On-site

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. • ...

Brasfield & Gorrie, LLC

Energy Marshal

Atlanta, GA · On-site

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. • ...

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

Site Activation Study information

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How much do site activation study jobs pay per hour?

As of Sep 8, 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 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 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 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 are popular job titles related to Site Activation Study jobs in Decatur, GA?

For Site Activation Study jobs in Decatur, GA, the most frequently searched job titles are:

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

Director, Study Operations

The START Center for Cancer Research

Atlanta, GA • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 11 days ago

Job description

The START Center for Cancer Research ("START") is the world's largest early phase site network, fully dedicated to oncology clinical research. Throughout our history, START has provided hope to cancer patients in global community practices by offering "Hope Through Access" to cutting edge trials throughout the United States and Europe.
We are seeking a Director of Study Operations. This role will lead research operations, ensuring all aspects of study conduct are performed according to START standards, regulatory standards, and with highest quality patient care. This role provides direction and oversight to the Clinical Research Coordinator, Data Coordinator and Medical Records teams with a high degree of autonomy. The Director, Study Operations collaborates closely with the Director, Nursing and Shared Services teams to support overall clinic operations, Study Acquisition / Activation and Quality Assurance activities. In addition, this role will provide direction for: department processes, training, employee recruitment, retention, and supervision for their areas of responsibility.
Work Schedule: Monday-Friday 8:00am-5:00pm
Location: Atlanta, Georgia
Essential Responsibilities:
  • Provide effective, proactive leadership to Clinical Research Coordinator team, Data Coordination team and Medical Records to ensure quality care delivery and ability to meet site specific key performance indicators.
  • Provide effective training and demonstrate competency of staff and management team for respective job roles.
  • Ensure timely and effective data management and communication with monitors and auditors, full compliance with GCP, and training documentation for all data management staff. Uphold all SOPs, including their review and revision as described in the Global QMS program.
  • Support study acquisition and activation functions in collaboration with global shared services team to meet START goals for speedy study start up and network-wide study acquisition functions, including facilitating protocol review meetings and overseeing accurate data collection and documentation in Veeva and any other required systems.
  • Ensure departments are using efficient, effective processes and systems to support patient care workflows and compliant care delivery in the context of clinical research protocols.
  • Use continuous process improvement techniques to proactively identify and address areas of improvement for the good of the patients, team members and the organization as a whole.
  • Review all incoming protocols for feasibility with respect to clinical research operations, specifically research coordinator teams.
  • Ensure effective inter-departmental interaction and communication with other support departments including regulatory, quality, site development, pharmacy and finance to ensure successful care delivery and compliance with all federal, GCP and regulatory agency requirements.
  • Support effective use and implementation of CTMS system, EHR system, and other necessary software to ensure appropriate and accurate documentation and data capture in the departments of responsibility.
  • Collaborate with other department leaders to proactively identify and address areas for process improvement.
  • Collaborate with Director, Nursing to lead site operations and act as a change agent for strategic project efforts both at the local level and regionally.

Required Education and Experience:
  • Bachelor's degree
  • 5 years of leadership experience in an oncology clinical research setting.
  • CITI GCP training.
  • Knowledge of GCP, GDPR and federal clinical research regulations required in US.
  • Must be familiar with Microsoft Office applications and clinical documentation systems.

Preferred Education and Experience:
  • Master's degree in health administration, nursing or other related field
  • BLS/ACLS

Physical and Travel Requirements:
  • Approximately 80% of time is spent sitting.
  • Very fast-paced and ever-changing healthcare environment.
  • Demanding deadlines and time frames.
  • Constant demand for updating knowledge.
  • Works closely with physicians and ancillary personnel in caring for and treating oncology/hematology patients.
  • Intermittent travel, less than quarterly, to support new site activation

Best-in-Class Benefits and Perks
We value the time, talent, and dedication our employees bring to START. Our commitment to your well-being and growth is reflected in a competitive compensation package-based on experience-along with comprehensive benefits designed to support you both personally and professionally:
  • 401(k) retirement savings plan with employer match
  • Eligibility for an annual performance bonus, based on role and company results
  • Generous paid time off and paid holidays
  • Comprehensive medical, dental, and vision coverage and optional insurance options
  • Company paid life and disability insurance for added financial protection
  • Employee Assistance Program (EAP) providing confidential, no -cost support for you and your family from day one
  • Flexible FSA and HSA plans to support your financial wellness
  • Commitment to a supportive environment that values balance, wellbeing, and flexibility
  • We're committed to fostering a collaborative, creative workplace where every team member is encouraged to contribute. At START, you'll join a team that values continuous learning, professional growth, shared ideas, and a culture built on inclusivity and innovation.

More About START
START clinical trial sites have conducted more than 1,000 early-phase clinical trials, including dozens of therapies that were approved by the FDA or EMA. START represents the world's largest roster of early-phase principal investigators across its Network of clinical trial sites. Committed to accelerating passage from trials to treatments, START delivers hope to patients, families, and physicians around the world via our mission of "Hope Through Access".
Learn more atSTARTresearch.com.
Ready to be part of a team changing the future of cancer treatment?
Join us in our mission to conquer cancer, one clinical trial at a time. Your expertise and dedication can help us bring hope and healing to patients worldwide. Please submit your application online.
We are an equal opportunity employer that welcomes and encourages diversity in the workplace. We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law.

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