Clinical Research Jobs in Georgia
Clinical Research jobs in Georgia are in strong and growing demand, concentrated in pharmaceutical development, academic medical centers, and biotech, with openings at every level from entry-level research coordinator through principal investigator and clinical operations director. Atlanta, Athens, and Augusta are the primary hiring hubs, anchored by employers such as Emory University, Piedmont Healthcare, and Pfizer's Georgia operations. The most consistently sought specialties in Georgia include oncology trials, cardiovascular research, and regulatory affairs coordination. Find a role that fits below and apply directly.
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Overview
As a temporary Assistant Clinical Trial Navigator with Javara, you will assist with the coordination and administration of clinical trials and report to the Manager of Site Operations and the Principal Investigator or designee. You will participate in achieving and exceeding patient enrollment goals with a dedication to quality and integrity. With a guiding principle of research participant safety, you will assist with implementing and coordinating research study procedures for the successful management of clinical trials.
Responsibilities:
- Seek to improve the patient’s experience, never compromising on safety.
- Provide excellent customer service to patients and participants, healthcare partner and practice stat investigators, sponsors, and vendors.
- Support enrollment goals by contributing to enrollment strategies, striving to provide exceptional experiences for patients, and building relationships with local patient populations.
- Assist with patient identification and recruitment as needed.
- Assist in strengthening efficient working relationships with colleagues, patients, investigators, and other internal and external partners.
- Ensure scientific integrity of data and record source data appropriately and accurately inclusive of patient visit data within source, CTMS, electronic reporting systems, completing the sponsor’s case report form, and timely query resolution.
- Assist with ensuring study documentation is up to date and audit ready.
- Adhere to all Standard Operating Procedures (SOPs), Good Clinical Practices (GCPs), protocols, OSHA, proper PPE usage and other regulatory authority requirements.
- Assist with conducting and documenting the informed consent process.
- Demonstrate continuous commitment to learning and developing skill sets and knowledge base as it relates to clinical trial operations and the patient experience.
- Coordinate and schedule patient visits and conduct visits per protocols.
- Assist with performing clinical and laboratory skills such as therapeutic area specifics, obtaining vitals, EKGs, and collecting, processing, and shipping bodily samples.
- Demonstrate our Core Values such as fostering teamwork and collaboration and cultivating relationships with healthcare system representatives.
- Additional tasks as assigned.
Qualifications:
- Associates or Bachelor’s Degree in related field or equivalent experience highly beneficial.
Work Environment:
The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job.
- This job operates in a professional environment.
- The noise level in this work environment is usually light to moderate.
Physical Demands:
The physical demands described here are representative of those that must be met to successfully perform the essential functions of this position. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of this job.
- The employee will regularly use hands to reach, handle or feel objects, tools, or controls and talk and hear.
- The employee may frequently stand, walk and sit.
- The employee may occasionally lift and/or move up to 25 pounds.
- Specific vision abilities required include close vision, distance vision and the ability to adjust focus.
Travel: This position may require up to 20% travel regionally but may occasionally include travel to other regions or Javara headquarters in Winston-Salem, NC.
Pre-Employment Screening: Drug screen and background check required.
This job description covers the most essential functions of this position and is not designed to contain a comprehensive listing of activities, duties or responsibilities that are required of the employee in this job. Duties, responsibilities, and activities may change at any time with or without notice.
Job Type: Full-time
Pay: From $20.00 per hour
Expected hours: 40.0 per week
Work Location: In person
Overview
As a temporary Assistant Clinical Trial Navigator with Javara, you will assist with the coordination and administration of clinical trials and report to the Manager of Site Operations and the Principal Investigator or designee. You will participate in achieving and exceeding patient enrollment goals with a dedication to quality and integrity. With a guiding principle of research participant safety, you will assist with implementing and coordinating research study procedures for the successful management of clinical trials.
Responsibilities:
- Seek to improve the patient’s experience, never compromising on safety.
- Provide excellent customer service to patients and participants, healthcare partner and practice stat investigators, sponsors, and vendors.
- Support enrollment goals by contributing to enrollment strategies, striving to provide exceptional experiences for patients, and building relationships with local patient populations.
- Assist with patient identification and recruitment as needed.
- Assist in strengthening efficient working relationships with colleagues, patients, investigators, and other internal and external partners.
- Ensure scientific integrity of data and record source data appropriately and accurately inclusive of patient visit data within source, CTMS, electronic reporting systems, completing the sponsor’s case report form, and timely query resolution.
- Assist with ensuring study documentation is up to date and audit ready.
- Adhere to all Standard Operating Procedures (SOPs), Good Clinical Practices (GCPs), protocols, OSHA, proper PPE usage and other regulatory authority requirements.
- Assist with conducting and documenting the informed consent process.
- Demonstrate continuous commitment to learning and developing skill sets and knowledge base as it relates to clinical trial operations and the patient experience.
- Coordinate and schedule patient visits and conduct visits per protocols.
- Assist with performing clinical and laboratory skills such as therapeutic area specifics, obtaining vitals, EKGs, and collecting, processing, and shipping bodily samples.
- Demonstrate our Core Values such as fostering teamwork and collaboration and cultivating relationships with healthcare system representatives.
- Additional tasks as assigned.
Qualifications:
- Associates or Bachelor’s Degree in related field or equivalent experience highly beneficial.
Work Environment:
The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job.
- This job operates in a professional environment.
- The noise level in this work environment is usually light to moderate.
Physical Demands:
The physical demands described here are representative of those that must be met to successfully perform the essential functions of this position. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of this job.
- The employee will regularly use hands to reach, handle or feel objects, tools, or controls and talk and hear.
- The employee may frequently stand, walk and sit.
- The employee may occasionally lift and/or move up to 25 pounds.
- Specific vision abilities required include close vision, distance vision and the ability to adjust focus.
Travel: This position may require up to 20% travel regionally but may occasionally include travel to other regions or Javara headquarters in Winston-Salem, NC.
Pre-Employment Screening: Drug screen and background check required.
This job description covers the most essential functions of this position and is not designed to contain a comprehensive listing of activities, duties or responsibilities that are required of the employee in this job. Duties, responsibilities, and activities may change at any time with or without notice.
Job Type: Full-time
Pay: From $20.00 per hour
Expected hours: 40.0 per week
Work Location: In person
See All 34 Clinical Research Jobs in Georgia
Find roles in Georgia that match your experience and apply in just a few clicks.
Find Clinical Research JobsClinical Research Jobs by City in Georgia
Where Georgia roles are concentrated, by current openings.
Clinical Research Job Market in Georgia
A snapshot from current Georgia openings, updated as new roles post.
Who's Hiring
Top Industries Hiring
- Education
- Healthcare & Medical Services
What Georgia Employers Look For
The qualifications that appear most often in clinical research jobs across Georgia.
- Bachelor's degree in life sciences, nursing, or a related clinical field required
- ACRP or SOCRA certification (CCRC, CCRP) strongly preferred by Georgia employers
- Experience with ICH-GCP guidelines and FDA regulatory requirements for clinical trials
- Proficiency in electronic data capture systems such as Medidata Rave or Oracle Clinical
- Ability to coordinate IRB submissions and maintain study documentation to audit-ready standards
- Strong written communication skills for protocol deviation reporting and sponsor interactions
Clinical Research Jobs in Georgia: Frequently Asked Questions
How do you become a clinical research in Georgia?
The most direct path into clinical research in Georgia is a bachelor's degree in a life sciences, nursing, or health-related field, followed by an entry-level role such as clinical research coordinator. Georgia does not require a state-issued license specific to clinical research, but most Georgia employers expect or strongly prefer certification from the Association of Clinical Research Professionals or the Society of Clinical Research Associates, earned by passing the CCRC or CCRP exam after meeting their experience requirements.
Which companies hire clinical researchs in Georgia?
Employers hiring clinical researchs in Georgia right now include Emory University, Alcanza Clinical Research, and Javara, based on current listings on Migrate Mate as of August 2026. Georgia's concentration of academic health systems and pharmaceutical contract research organizations means hiring is active across both large institutions and specialized CRO sites throughout the state.
Which Georgia cities have the most clinical research jobs?
Atlanta, Decatur, and Woodstock account for the largest share of clinical research openings in Georgia. Atlanta dominates because of its density of academic medical centers, hospital systems, and CRO offices, while Athens and Augusta draw openings through the University of Georgia's research programs and Augusta University's medical campus, which together support a steady pipeline of trial activity outside the metro.
Are there remote clinical research jobs in Georgia?
Yes, but they are less common than in purely desk-based fields, since many clinical research roles require on-site patient contact, facility access, or monitoring visits. About 43% of clinical research openings tied to Georgia are remote or hybrid as of August 2026, reflecting the portion of the field that is administrative or data-focused. Roles most likely to be remote include clinical data management, regulatory submissions, and sponsor-side monitoring coordination.
How can I get hired as a clinical research in Georgia with little or no experience?
The most realistic entry path is applying for a clinical research coordinator I or study coordinator role at one of Georgia's large academic health systems, where Emory Healthcare, Augusta University Health, and Grady Health System regularly hire candidates coming directly from undergraduate life sciences or nursing programs. A completed Good Clinical Practice certification and any hands-on exposure through a clinical internship or as a medical scribe or patient care technician significantly strengthens an application for these new-graduate-level positions.
Where can I find and apply to clinical research jobs in Georgia?
You can find and apply to clinical research jobs in Georgia on Migrate Mate, which lists current Georgia openings across Atlanta, Augusta, Athens, and other locations in the state. Search the listings to find roles that match your experience level and specialty, then apply directly to the ones that fit.
See All 34 Clinical Research Jobs in Georgia
Find roles in Georgia that match your experience and apply in just a few clicks.
Find Clinical Research Jobs