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Clinical Study Startup Jobs in Georgia (NOW HIRING)

JobRx, Inc.

Medical Science Liaison

Atlanta, GA · On-site

$180 - $187.50/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

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 ...

IQVIA

CRA 1, IQVIA Biotech

Marietta, GA

$71K - $145K/yr

... clinical research studies by performing site monitoring and site management activities. In this ... startup activities based on study needs. Accurate and timely documentation is critical. The CRA I ...

IQVIA

CRA 1, IQVIA Biotech

Marietta, GA · On-site

$71K - $145K/yr

... clinical research studies by performing site monitoring and site management activities. In this ... startup activities based on study needs. Accurate and timely documentation is critical. The CRA I ...

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How much do clinical study startup jobs pay per hour?

As of Aug 18, 2026, the average hourly pay for clinical study startup 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 is a clinical study startup?

A Clinical Study Startup job involves managing the initial phases of a clinical trial, ensuring all regulatory, ethical, and logistical requirements are met before patient enrollment begins. Responsibilities typically include submitting regulatory documents, coordinating with ethics committees, negotiating contracts, and ensuring trial sites are fully prepared. This role requires strong knowledge of clinical research regulations, timelines, and collaboration with internal and external stakeholders. Effective study startup is crucial for minimizing delays and ensuring compliance with industry standards.

What are the typical responsibilities of someone working in clinical study startup?

Professionals in Clinical Study Startup are primarily responsible for coordinating and executing study initiation activities, including regulatory document collection, ethics submissions, site contracting, and start-up logistics. They work closely with investigators, sponsors, and cross-functional teams to ensure all regulatory and site requirements are met before the clinical trial begins. This role often involves tight deadlines and frequent communication with stakeholders both internally and externally. It's a fast-paced position that is ideal for individuals who enjoy detail-oriented work and project coordination in a collaborative environment.

What are the key skills and qualifications needed to thrive in clinical study startup, and why are they important?

Success in a Clinical Study Startup role requires a strong understanding of clinical research processes, regulatory requirements, project management, and often a life sciences degree or related field. Familiarity with clinical trial management systems (CTMS), electronic trial master files (eTMF), and regulatory submission platforms is essential, along with certifications like GCP (Good Clinical Practice) being advantageous. Attention to detail, proactive problem-solving, and excellent organizational and communication skills help candidates excel. These qualifications ensure smooth study initiation, regulatory compliance, and effective cross-functional collaboration within demanding timelines.

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 jobs in Georgia?

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

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

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

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

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

Clinical Study Startup jobs near you
Infographic showing various Clinical Study Startup job openings in Georgia as of August 2026, with employment types broken down into 100% Full Time. Highlights an 72% In-person, 14% Hybrid, and 14% Remote job distribution, with an average salary of $109,799 per year, or $52.8 per hour.

Clinical Research Manager (68740)

ATLANTA GASTRO

Atlanta, GA • On-site

Full-time

Posted 11 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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