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Clinical Study Startup Manager Jobs in Georgia (NOW HIRING)

United-Digestive

Clinical Research Manager

Atlanta, GA · On-site

$100 - $125/hr

Demonstrated experience managing study startup, site activation, conduct, monitoring, closeout, and ... Master's degree in clinical research, healthcare administration, public health, nursing, or a ...

Syneos Health

Medical Science Liaison

Atlanta, GA · On-site

$200 - $250/hr

Partner with Clinical Development, Clinical Operations, CRO partners, and investigative sites to support effective study startup, protocol understanding, and trial execution. * Execute nonpromotional ...

Becton, Dickinson and Company

Study & Site Management * Serve as CRA for assigned complex clinical studies, providing expert oversight of site selection, initiation, monitoring, and closeout activities (onsite, virtual, remote)

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How much do clinical study startup manager jobs pay per hour?

As of Sep 7, 2026, the average hourly pay for clinical study startup manager 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 does a clinical study startup manager do?

A Clinical Study Startup Manager oversees the initial phases of clinical trials, ensuring all regulatory, ethical, and site-specific requirements are met before a study begins. They coordinate activities such as site selection, contract negotiation, budget management, and regulatory submissions. Their goal is to streamline the startup process to minimize delays and ensure compliance with industry standards, facilitating a smooth transition to patient enrollment and study execution.

What are the key skills and qualifications needed to thrive as a clinical study startup manager?

A Clinical Study Startup Manager requires expertise in clinical research processes, regulatory compliance, and project management, often 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 typically expected. Strong organizational, communication, and stakeholder management skills help facilitate collaboration and timely study initiation. These skills ensure smooth, compliant, and efficient study startup, which is critical for the overall success and timelines of clinical trials.

What are some common challenges faced by clinical study startup managers during the site activation process?

Clinical Study Startup Managers often encounter challenges such as varying regulatory requirements across regions, delays in site contract negotiations, and managing the collection of essential documents from multiple stakeholders. Coordinating with cross-functional teams—including regulatory affairs, legal, and clinical operations—requires strong project management and communication skills to keep timelines on track. Anticipating potential bottlenecks and proactively addressing site-specific concerns are critical for ensuring a smooth and timely study startup.

What is the difference between Clinical Study Startup Manager vs Clinical Research Coordinator?

AspectClinical Study Startup ManagerClinical Research Coordinator
ResponsibilitiesOversees study initiation, site selection, regulatory submissions, and startup activitiesManages participant recruitment, data collection, and day-to-day study operations at sites
Required CredentialsBachelor's degree, clinical research experience, knowledge of regulationsBachelor's degree, clinical research experience, good clinical practice (GCP) training
Work EnvironmentCorporate or sponsor offices, clinical trial sitesClinical trial sites, hospitals, research centers

The Clinical Study Startup Manager focuses on preparing and initiating clinical trials, ensuring regulatory compliance and site readiness. In contrast, the Clinical Research Coordinator handles the daily operations at trial sites, managing participant interactions and data collection. Both roles require similar credentials and work in related environments, but their core responsibilities differ significantly.

What are the most commonly searched types of Clinical Study Startup jobs in Georgia?

The most popular types of Clinical Study Startup jobs in Georgia are:

What are popular job titles related to Clinical Study Startup Manager jobs in Georgia?

For Clinical Study Startup Manager jobs in Georgia, the most frequently searched job titles are:

What job categories do people searching Clinical Study Startup Manager jobs in Georgia look for?

The top searched job categories for Clinical Study Startup Manager jobs in Georgia are:

What cities in Georgia are hiring for Clinical Study Startup Manager jobs?

Cities in Georgia with the most Clinical Study Startup Manager job openings:

Clinical Study Startup Manager jobs near you
Infographic showing various Clinical Study Startup Manager job openings in Georgia as of August 2026, with employment types broken down into 85% Full Time, 13% Part Time, and 2% Contract. Highlights an 88% Physical, 2% Hybrid, and 10% Remote job distribution, with an average salary of $109,799 per year, or $52.8 per hour.

Clinical Research Manager

United-Digestive

Atlanta, GA • On-site

$100 - $125/hr

Other

Posted 6 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/InternsLead day-to-day multi-site clinical research operations and promote consistent, efficient study executionManage the study lifecycle from feasibility and startup through conduct, monitoring, and closeoutTrack enrollment, timelines, milestones, compliance, and data quality; resolve issues and escalate significant risksServe as the operational liaison among investigators, sponsors, CROs, vendors, staff, and centralized support teamsEnsure regulatory documentation and study activities meet FDA, ICH-GCP, HIPAA, IRB, sponsor, and organizational requirementsConduct quality reviews, implement SOPs and CAPAs, and maintain audit and inspection readinessRecruit, onboard, train, mentor, evaluate, and allocate research staff based on study and site prioritiesSupport research systems, standardized workflows, and practical process improvements across sitesEDUCATION, SKILLS, & EXPERIENCE:Required:Bachelor's degree in nursing, life sciences, public health, healthcare administration, or a related fieldAt 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 workflowsKnowledge of FDA regulations, ICH-GCP, HIPAA, and IRB requirements, with strong project management, people-leadership, communication, and organizational skillsPreferred:Master's degree in clinical research, healthcare administration, public health, nursing, or a related fieldClinical research certification and experience with research systems and process improvementWORK 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.IND123 #J-18808-Ljbffr

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