ZipRecruiter

Log In

1

Clinical Research Associate Jobs in Pooler, GA (NOW HIRING)

Javara Inc.

Be Seen First

Clinical Research Coordinator (On-Site)

Savannah, GA · On-site

$25/hr

As a Clinical Research Coordinator/Clinical Trial Navigator I with Javara, you will be responsible ... Associates or Bachelor's Degree in related field or equivalent industry experience. * 1+ years ...

Centricity Research

Clinical Screening Coordinator

Rincon, GA · On-site

$22 - $29.25/hr

Centricity Research is one of the largest clinical research networks in North America. We are a fully centralized Integrated Research Organization (IRO) specializing in conducting Phase I-IV clinical ...

CenExel

Study Startup Specialist I

Savannah, GA · On-site

About Us: CenExel is a leading nationwide clinical research site and patient network serving the life sciences industry. Leading in CNS and early phase studies, our 18 science-led Centers of ...

Javara Inc.

Clinical Trial Navigator I

Savannah, GA · On-site

Inform and educate the research team and healthcare system staff regarding study related procedures ... Associates or Bachelor's Degree in related field or equivalent industry experience. * 1+ years ...

Javara

Clinical Trial Navigator I

Savannah, GA · On-site

Inform and educate the research team and healthcare system staff regarding study related procedures ... Associates or Bachelor's Degree in related field or equivalent industry experience. * 1+ years ...

Javara

Clinical Trial Navigator I

Savannah, GA · On-site

Inform and educate the research team and healthcare system staff regarding study related procedures ... Associates or Bachelor's Degree in related field or equivalent industry experience. * 1+ years ...

Compass Group

Clinical Dietitian

Savannah, GA · On-site

Apply the latest research in alignment with the diet manual, company policies, and facility ... Click here to Learn More about the Compass Story Associates may be eligible for additional paid and ...

Compass Group

Clinical Dietitian

Savannah, GA · On-site

Apply the latest research in alignment with the diet manual, company policies, and facility ... Click here to Learn More about the Compass Story Associates may be eligible for additional paid and ...

Compass Group

Clinical Dietitian

Savannah, GA · On-site

Apply the latest research in alignment with the diet manual, company policies, and facility ... Click here to Learn More about the Compass Story Associates may be eligible for additional paid and ...

Compass Group

Clinical Dietitian

Savannah, GA · On-site

Apply the latest research in alignment with the diet manual, company policies, and facility ... Click here to Learn More about the Compass Story Associates may be eligible for additional paid and ...

Compass Group

Clinical Dietitian

Springfield, GA · On-site

Apply the latest research in alignment with the diet manual, company policies, and facility ... Click here to Learn More about the Compass Story Associates may be eligible for additional paid and ...

Compass Group

Clinical Dietitian

Springfield, GA · On-site

Apply the latest research in alignment with the diet manual, company policies, and facility ... Click here to Learn More about the Compass Story Associates may be eligible for additional paid and ...

Compass Group

Clinical Dietitian

Springfield, GA · On-site

Apply the latest research in alignment with the diet manual, company policies, and facility ... Click here to Learn More about the Compass Story Associates may be eligible for additional paid and ...

Compass Group

Clinical Dietitian

Springfield, GA · On-site

Apply the latest research in alignment with the diet manual, company policies, and facility ... Click here to Learn More about the Compass Story Associates may be eligible for additional paid and ...

next page

Showing results 1-20

All JobsClinical Research Associate JobsClinical Research Associate Jobs in Pooler, GA

Clinical Research Associate information

See Pooler, GA salary details

$10

$37

$63

How much do clinical research associate jobs pay per hour?

As of Aug 7, 2026, the average hourly pay for clinical research associate in Pooler, GA is $37.36, according to ZipRecruiter salary data. Most workers in this role earn between $26.20 and $47.84 per hour, depending on experience, location, and employer.

Is it hard to get a clinical research associate job?

Securing a clinical research associate (CRA) position can be competitive, often requiring a relevant degree such as a life sciences or healthcare-related field, along with experience in clinical trials. Strong organizational skills, knowledge of Good Clinical Practice (GCP), and familiarity with clinical trial management systems can improve job prospects, but entry may be challenging for those without relevant qualifications or experience.

What is a clinical research associate?

Clinical Research Associates (CRAs) are professionals responsible for monitoring and overseeing clinical trials to ensure they are conducted in accordance with regulatory guidelines, protocols, and ethical standards. They play a key role in ensuring the safety of trial participants and the integrity of collected data. CRAs often visit clinical trial sites to verify data accuracy, maintain study documentation, and provide training to site staff. Their work ensures that new drugs, treatments, or medical devices are tested rigorously before they reach the market.

What are the key skills and qualifications needed to thrive as a clinical research associate?

To thrive as a Clinical Research Associate, you need a solid background in life sciences, attention to detail, and experience with clinical trial protocols, often supported by a relevant bachelor's degree. Familiarity with electronic data capture (EDC) systems, Good Clinical Practice (GCP) guidelines, and sometimes certifications like ACRP or SOCRA is typically required. Strong organizational, communication, and problem-solving skills help build effective relationships with research sites and ensure compliance. These skills are vital for maintaining the integrity of clinical trials, ensuring regulatory adherence, and advancing medical research efficiently.

What is the difference between Clinical Research Associate vs Clinical Trial Coordinator?

AspectClinical Research AssociateClinical Trial Coordinator
CredentialsBachelor's degree, often with clinical research certificationsBachelor's degree, often with clinical research or healthcare certifications
Work EnvironmentMonitors clinical sites, reviews data, ensures complianceCoordinates trial activities, manages schedules, and communicates with sites
Employer & IndustryPharmaceutical companies, CROs, biotech firmsHospitals, research institutions, CROs

Both roles are essential in clinical trials, with CRAs focusing on site monitoring and compliance, while Clinical Trial Coordinators handle day-to-day trial management. They often collaborate but have distinct responsibilities within the clinical research process.

Is being a clinical research associate worth it?

A clinical research associate (CRA) monitors clinical trials to ensure compliance with protocols and regulations, often requiring strong organizational and communication skills. The role offers opportunities for career growth, competitive salaries, and the chance to contribute to medical advancements, but it can involve irregular hours and travel. Overall, it can be a rewarding career for those interested in healthcare and research.

What are some common challenges clinical research associates face when monitoring clinical trial sites?

Clinical Research Associates (CRAs) often encounter challenges such as ensuring protocol compliance across multiple sites, managing tight project timelines, and maintaining accurate documentation. Additionally, CRAs must effectively communicate with site staff to resolve issues and ensure data integrity, all while adhering to regulatory guidelines. Balancing frequent travel, adapting to different site environments, and handling unexpected issues such as patient recruitment delays are also typical aspects of the role.
More about Clinical Research Associate jobs
What are the most commonly searched types of Clinical Research jobs in Pooler, GA? The most popular types of Clinical Research jobs in Pooler, GA are:
What job categories do people searching Clinical Research Associate jobs in Pooler, GA look for? The top searched job categories for Clinical Research Associate jobs in Pooler, GA are:
What cities near Pooler, GA are hiring for Clinical Research Associate jobs? Cities near Pooler, GA with the most Clinical Research Associate job openings:
Clinical Research Associate jobs near you
Infographic showing various Clinical Research Associate job openings in Pooler, GA as of August 2026, with employment types broken down into 2% As Needed, 73% Full Time, 18% Part Time, and 7% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $77,717 per year, or $37.4 per hour.

Clinical Research Coordinator - Clinical Research

CenExel

Savannah, GA • On-site

$25 - $29/hr

Full-time

Medical, Dental, Vision, Life, Retirement

Re-posted 21 days ago

CenExel rating

7.5

Company rating: 7.5 out of 10

Based on 6 frontline employees who took The Breakroom Quiz

65th of 120 rated laboratories

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.

What CenExel employees say

Pay

Hours and flexibility

Workplace

Get the full story on Breakroom

Apply