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From Home Clinical Research Rater Jobs in Georgia

Denali Health

Clinical Research Nurse

Atlanta, GA · On-site

Competitive PRN hourly rate * Flexible scheduling to accommodate your availability * Opportunity to work on cutting-edge clinical research * Exposure to diverse therapeutic areas and study phases

Denali Health

Clinical Research Nurse

Atlanta, GA · On-site

Competitive PRN hourly rate * Flexible scheduling to accommodate your availability * Opportunity to work on cutting-edge clinical research * Exposure to diverse therapeutic areas and study phases

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All JobsClinical Research Rater JobsFrom Home Clinical Research Rater JobsFrom Home Clinical Research Rater Jobs in Georgia

From Home Clinical Research Rater information

What is the difference between From Home Clinical Research Rater vs From Home Clinical Trial Coordinator?

AspectFrom Home Clinical Research RaterFrom Home Clinical Trial Coordinator
CredentialsTypically requires a high school diploma or equivalent; some roles prefer healthcare or research experienceRequires a bachelor's degree in health sciences, nursing, or related fields; certification may be preferred
Work EnvironmentRemote, primarily computer-based, evaluating patient data and reportsPrimarily remote or hybrid; involves coordinating trial activities, communicating with sites and sponsors
Employer & Industry UsageUsed by research organizations, pharmaceutical companies, and CROs for data evaluationUsed by clinical research sites, pharmaceutical companies, and CROs for trial management

While both roles are involved in clinical research, From Home Clinical Research Raters focus on evaluating patient data remotely, whereas From Home Clinical Trial Coordinators manage trial logistics and communication. Understanding these differences helps job seekers identify the right position based on their skills and credentials.

What are the most commonly searched types of Clinical Research Rater jobs in Georgia?

The most popular types of Clinical Research Rater jobs in Georgia are:

What are popular job titles related to From Home Clinical Research Rater jobs in Georgia?

For From Home Clinical Research Rater jobs in Georgia, the most frequently searched job titles are:

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The top searched job categories for From Home Clinical Research Rater jobs in Georgia are:

What cities in Georgia are hiring for From Home Clinical Research Rater jobs?

Cities in Georgia with the most From Home Clinical Research Rater job openings:

From Home Clinical Research Rater jobs near you
Infographic showing various From Home Clinical Research Rater job openings in Georgia as of August 2026, with employment types broken down into 67% Full Time, and 33% Part Time. Highlights an 100% In-person job distribution.

Clinical Research Coordinator - Clinical Research

Savannah, GA • On-site

CenExel
Scientific Research and Development Services • 1 - 10 employees

7.5

Company rating: 7.5 out of 10

Based on 6 frontline employees who took The Breakroom Quiz

64th of 120 rated laboratories

Good employer

Uninterrupted breaks

Learn more about CenExelexternal

$25 - $29/hr

Full-time

Medical, Dental, Vision, Life, Retirement

Re-posted 10 days ago

Job description

About Us:
Each of CenExel's research sites specialize in Phase I to Phase IV clinical trials. Our Centers of Excellence comprise some of the most well respected and long-standing research facilities in the country. Specialty areas of research across our sites include Psychiatry, Acute Post Op Pain, Asian Bridging, Dermatology, GI, and Neurology. Each of our Centers of Excellence has tremendous experience and expertise in complex early phase trials, and all our sites have in-patient capability. We focus on quality people, teamwork, and highly experienced clinical research managers with a history of success.
Along with an exceptional work environment that promotes teamwork, positive leadership, and optimal work-life balance, CenExel Clinical Research also provides highly competitive compensation and a generous benefits package to full time employees after 30 days of employment including Health Insurance, Dental, Vision, LTD, STD, Life Ins, and 401k.
Schedule: Monday - Friday (08:00 AM - 4:30)
Hourly Rate: $25.00 - $29.00/hr (depending on education, experience, and skillset)
Job Summary:
Responsible for coordinating all aspects of clinical trials with the strictest adherence to ICH (International Conference on Harmonization), GCP (Good Clinical Practices), protocol, and company guidelines, regulations, and policies.
Essential Responsibilities and Duties:
  • Under supervision, coordinates aspects of patient involvement for complex and/or multiple studies from study initiation until study completion.
  • Organizes research information for clinical trials.
  • Observes subjects and assists with data analysis and reporting.
  • Schedules the collection of data.
  • Reviews, and reports adverse events, protocol deviations, and other unanticipated problems appropriately.
  • Monitors, and reports research data to maintain quality and compliance.
  • Performs administrative and regulatory duties related to the study as appropriate.
  • Participates in other protocol development activities.
  • Ensures site receives accurate information and supplies from sponsors (i.e.: source, protocol, scales, supplies, approvals, contacts, etc.)
  • Educates potential participants and caregivers on protocol specific details and expectations.
  • Performs safety and efficacy assessments per protocol (vital signs, EKGs, blood draws and other assessments as assigned).
  • Assists Clinical Trial Manager (CTM) with oversight of vendors, accounting, regulatory, client satisfaction, recruitment, quality, and trial outcomes.
  • Assists the CTM in planning, creating processes, trainings and development of staff.
  • Assumes other duties and responsibilities as assigned. The above responsibilities are a general description of the level and nature of the work assigned to this classification and are not to be considered as all inclusive.

Education/Experience/Skills:
  • Must have experience and demonstrate mastery of a Clinical Research Coordinator position.
  • High school graduate or equivalent; Bachelors Degree, preferred
  • CCRC certification preferred
  • 2-3 years of experience in the medical field, preferred
  • Knowledge and understanding of Federal regulations protecting human subjects in research and that govern the conduct of clinical trials.
  • Strong leadership and mentorship skills.
  • Developing and maintaining effective working relationships at all levels of the organization, along with those at the sponsor and vendor level.
  • Crisis management and problem solving skills; ability to react calmly and effectively in emergent situations.
  • Works independently as well as functioning as part of a team.
  • Must be able to effectively communicate verbally and in writing.

Working Conditions
  1. Indoor, Office environment.
  2. Shift work, depending on location.
  3. Essential physical requirements include sitting, typing, standing, and walking.
  4. Lightly active position, occasional lifting of up to 20 pounds.
  5. Reporting to work, as scheduled, is essential.
  6. Overnight travel may be required for training and/or investigative meetings.

CenExel Clinical Research is an Equal Opportunity Employer. All applicants will be considered for employment without regards to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran, or status.
Equal Opportunity Employer
This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor.

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