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Seasonal Clinical Study Startup Jobs in Decatur, GA

Syneos Health

Medical Science Liaison

Atlanta, GA · On-site

$190 - $210/hr

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

Syneos Health, Inc.

Medical Science Liaison

Atlanta, GA · On-site

$190 - $210/hr

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

Amgen

Imaging Specialist Manager

Atlanta, GA · On-site +1

... clinical trials across all phases from study start-up to close-out. Responsabilities: * Provide oversight and expertise for imaging setup and startup activities * Maintain the quality and scientific ...

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All JobsClinical Study Startup JobsSeasonal Clinical Study Startup JobsSeasonal Clinical Study Startup Jobs in Decatur, GA

Seasonal Clinical Study Startup information

See Decatur, GA salary details

$21.5K

$122.3K

$201.1K

How much do seasonal clinical study startup jobs pay per year?

As of Aug 29, 2026, the average yearly pay for seasonal clinical study startup in Decatur, GA is $122,325.00, according to ZipRecruiter salary data. Most workers in this role earn between $83,000.00 and $153,300.00 per year, depending on experience, location, and employer.

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

AspectSeasonal Clinical Study StartupClinical Research Coordinator
CredentialsTypically requires a bachelor's degree in health sciences or related field; certifications like CCRP are a plusRequires a bachelor's degree; certifications like CCRP or CCRC are common
Work EnvironmentPrimarily in clinical trial sites, hospitals, or research centers during specific seasonsIn clinical settings, hospitals, or research facilities year-round
Employer & Industry UsageUsed by pharmaceutical companies, CROs, and research institutions for seasonal trial phasesCommonly employed by research sites, hospitals, and academic institutions

Seasonal Clinical Study Startup focuses on preparing and initiating clinical trials during specific periods, often involving planning, regulatory submissions, and site readiness. In contrast, a Clinical Research Coordinator manages ongoing clinical trials, ensuring protocol adherence, patient recruitment, and data collection throughout the study duration. Both roles require similar credentials but differ mainly in scope and timing of responsibilities.

What job categories do people searching Seasonal Clinical Study Startup jobs in Decatur, GA look for?

The top searched job categories for Seasonal Clinical Study Startup jobs in Decatur, GA are:

What cities near Decatur, GA are hiring for Seasonal Clinical Study Startup jobs?

Cities near Decatur, GA with the most Seasonal Clinical Study Startup job openings:

Seasonal Clinical Study Startup jobs near you
Infographic showing various Seasonal Clinical Study Startup job openings in Decatur, GA as of August 2026, with employment types broken down into 2% As Needed, 74% Full Time, 18% Part Time, and 6% Contract. Highlights an 85% Physical, 1% Hybrid, and 14% Remote job distribution, with an average salary of $122,325 per year, or $58.8 per hour.

Clinical Research Manager (68740)

ATLANTA GASTRO

Atlanta, GA • On-site

Full-time

Posted 21 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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