Clinical Research Manager Jobs in Georgia
Clinical Research Manager jobs in Georgia are in strong demand, concentrated in pharmaceutical research, academic medical centers, and contract research organizations, with openings at every level from coordinator-to-manager transitions through senior and principal positions. Atlanta, Augusta, and Savannah lead hiring activity, anchored by institutions and organizations such as Emory Healthcare, Mercer University, and Piedmont Healthcare. The most sought-after specialties in Georgia right now are oncology trials, cardiovascular research, and regulatory affairs-focused oversight roles. Find a role that fits below and apply directly.
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Showing 5 of 34+ Clinical Research Manager jobs
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 Manager Jobs in Georgia
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Find JobsClinical Research Manager Jobs by City in Georgia
Where Georgia roles are concentrated, by current openings.
Clinical Research Manager 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 manager jobs across Georgia.
- Bachelor's degree in life sciences, nursing, or a related clinical field required
- Minimum two to five years of clinical trial coordination or management experience preferred
- ACRP or SOCRA certification (CCRC, CCRP, or CRC) strongly preferred by Georgia employers
- Demonstrated knowledge of FDA regulations, ICH guidelines, and GCP standards
- Experience with electronic data capture systems such as Medidata Rave or REDCap
- Strong track of managing IRB submissions and regulatory document maintenance in Georgia settings
Clinical Research Manager Jobs in Georgia: Frequently Asked Questions
How do you become a clinical research manager in Georgia?
Most clinical research manager roles in Georgia require a bachelor's degree in a life science, nursing, or health-related field, followed by hands-on experience as a clinical research coordinator. Georgia does not require a state-issued license for this role, but employers consistently prefer candidates who hold a professional certification such as the CCRP from SOCRA or the CCRC from ACRP. Building experience at a Georgia hospital system, academic medical center, or contract research organization is the most direct path.
Which companies hire clinical research managers in Georgia?
Employers hiring clinical research managers 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 organizations means hiring is consistent throughout the year, not limited to seasonal cycles.
Which Georgia cities have the most clinical research manager jobs?
Atlanta, Decatur, and Woodstock have the most clinical research manager openings in Georgia. Atlanta drives the majority of volume as home to major academic medical centers and corporate headquarters, while Augusta's activity reflects the presence of Wellstar MCG Health and active research programs at Augusta University, giving mid-sized markets a meaningful share of openings.
Are there remote clinical research manager jobs in Georgia?
Yes, but they are less common than in purely desk-based fields, since many clinical research manager roles require on-site trial oversight, vendor meetings, and direct staff supervision. About 43% of clinical research manager openings tied to Georgia are remote or hybrid as of August 2026, reflecting selective flexibility. Regulatory affairs oversight, protocol writing, and sponsor-facing communication duties are the parts of the role most likely to be performed remotely.
How can I get hired as a clinical research manager in Georgia with little or no experience?
The most realistic entry path is securing a clinical research coordinator role first, since Georgia's larger employers including Emory University Hospital and Piedmont Healthcare regularly post coordinator positions that serve as a structured step into management. Candidates transitioning from adjacent roles such as research nurse, study monitor, or regulatory affairs associate are well-positioned. Earning a CCRP or CCRC certification before applying, even without managerial experience, signals readiness and improves competitiveness at Georgia academic and community health institutions.
Where can I find and apply to clinical research manager jobs in Georgia?
You can find and apply to clinical research manager jobs in Georgia on Migrate Mate, which lists current Georgia openings updated regularly. Find roles that fit your experience and location, then apply directly to the employer. No account or profile creation is needed to search and apply.
See All 34 Clinical Research Manager Jobs in Georgia
Find roles in Georgia that match your experience and apply in just a few clicks.
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