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Clinical Research Associate Monitor Jobs in Decatur, GA

Alcanza

Clinical Research Coordinator

Decatur, GA

$23.75 - $31.50/hr

Conducting monitoring visits and resolves issues as needed in a timely manner; * Ensuring study ... A Medical Assistant diploma, LPN/LVN, EMT credential OR Associate's degree AND a minimum of 1 year ...

CenExel

Clinical Research Coordinator

Decatur, GA · On-site

$23.75 - $31.50/hr

Monitors, and reports research data to maintain quality and compliance. * Performs administrative ... Assists Clinical Trial Manager (CTM) with oversight of vendors, accounting, regulatory, client ...

Care Access

Clinical Research Coordinator II

Decatur, GA

$23.75 - $31.50/hr

Monitors quality metrics; prevents deviations; resolves queries quickly. * Interact in a positive ... A minimum of 3 years prior Clinical Research Coordinator experience required * Prefer 1 year of ...

CenExel

Clinical Research RN

Decatur, GA · On-site

... monitoring of vitals, blood sugar, vital signs, lab tests, etc. * Reviews and executes clinical ... research protocols. * Completes and maintains study documents in accordance with sponsor and site ...

CenExel

Clinical Research RN

Decatur, GA · On-site

... monitoring of vitals, blood sugar, vital signs, lab tests, etc. * Reviews and executes clinical ... research protocols. * Completes and maintains study documents in accordance with sponsor and site ...

Care Access

Clinical Research Coordinator II

Decatur, GA

$23.75 - $31.50/hr

Monitors quality metrics; prevents deviations; resolves queries quickly. * Interact in a positive ... A minimum of 3 years prior Clinical Research Coordinator experience required  * Prefer 1 year of ...

CenExel

Clinical Research RN

Decatur, GA

... monitoring of vitals, blood sugar, vital signs, lab tests, etc. * Reviews and executes clinical ... research protocols. * Completes and maintains study documents in accordance with sponsor and site ...

Care Access

Clinical Research Coordinator II

Decatur, GA · On-site

$23.75 - $31.50/hr

Monitors quality metrics; prevents deviations; resolves queries quickly. * Interact in a positive ... A minimum of 3 years prior Clinical Research Coordinator experience required * Prefer 1 year of ...

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How much do clinical research associate monitor jobs pay per hour?

As of May 31, 2026, the average hourly pay for clinical research associate monitor in Decatur, GA is $40.15, according to ZipRecruiter salary data. Most workers in this role earn between $28.17 and $51.39 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Clinical Research Associate Monitor, and why are they important?

To thrive as a Clinical Research Associate Monitor, you need a solid understanding of clinical trial protocols, regulatory guidelines (such as GCP and FDA regulations), and often a degree in life sciences or a related field. Familiarity with electronic data capture (EDC) systems, clinical trial management systems (CTMS), and certifications like ACRP or SOCRA are typically required. Excellent attention to detail, strong organizational skills, and effective communication are crucial soft skills for liaising with site staff and ensuring protocol compliance. These competencies ensure that clinical trials are conducted ethically, accurately, and in adherence to regulatory standards, safeguarding data integrity and patient safety.

What are some common challenges Clinical Research Associate Monitors face when overseeing multiple clinical trial sites?

Clinical Research Associate Monitors often manage several clinical trial sites simultaneously, which can present challenges such as coordinating schedules, ensuring consistent protocol adherence, and managing documentation across diverse teams. Effective communication and strong organizational skills are crucial to address site-specific issues promptly and maintain regulatory compliance. Additionally, frequent travel and adapting to varying site cultures are common aspects of the role, and building strong relationships with site staff can greatly enhance trial success.

What is a Clinical Research Associate Monitor?

A Clinical Research Associate Monitor is a professional responsible for overseeing clinical trials to ensure they are conducted in accordance with regulatory requirements, Good Clinical Practice (GCP) guidelines, and study protocols. They monitor trial sites, review documentation, verify data accuracy, and ensure the safety and rights of study participants. Their work is crucial in maintaining the integrity of clinical research and facilitating the development of new medical treatments.
What job categories do people searching Clinical Research Associate Monitor jobs in Decatur, GA look for? The top searched job categories for Clinical Research Associate Monitor jobs in Decatur, GA are:
What cities near Decatur, GA are hiring for Clinical Research Associate Monitor jobs? Cities near Decatur, GA with the most Clinical Research Associate Monitor job openings:
Clinical Research Associate Monitor jobs near you
Clinical Research Assistant

Clinical Research Assistant

EyeSouth Partners LLC

Marietta, GA

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 4 days ago

EyeSouth Partners rating

6.2

Company rating: 6.2 out of 10

Based on 19 frontline employees who took The Breakroom Quiz

Job description

Georgia Retina, one of the largest retina-only medical practices in the Southeast, continues to provide patients with the most advanced medical treatments available for retinal diseases and disorders. With over 200 years of combined experience, Georgia Retina’s board-certified ophthalmologists offer world-class expertise and a personalized approach to patient care in 13 Metro Atlanta area locations.


We are now hiring for a Clinical Research Assistant that will support a high-volume Research Department within an ophthalmic practice that focuses on providing quality and compassionate care to each patient needing complete eye care services.


A CRA is responsible for performing procedures and coordinating the execution of clinical trials in accordance with research protocols.


• Recruit and screen subjects to participate in trials
• Coordinate patient visits and perform procedures related to research
• Collect accurate data obtained from research visits
• Monitor research participants to ensure adherence to study protocol
• Adhere to Good Clinical Practice (GCP) guidelines including regulatory and ethical standards
• Maintain relationships with site staff, study subjects, and sponsor delegates
• Perform other related duties as assigned by the Clinical Research Coordinator
• Maintain compliance with all research Standard Operating Procedures (SOPs)


EXPERIENCED 2-3 years in Clinical Research


• 2+ years in healthcare, preferably ophthalmology, but not necessarily in clinical research
• Analytical mindset
• Attention to detail
• Exceptional interpersonal skills
• Superior verbal and written communication skills
• Understanding of laboratory procedures and equipment
• Proficiency in MS Office – Word, Excel and Outlook
• High school diploma or equivalent GED


We offer a competitive benefits package to our employees:

• Medical
• Dental
• Vision
• 401k w/ Match
• HSA/FSA
• Telemedicine (100% company paid)
• EAP (100% company paid)
• Group Life/AD&D (100% company paid)
• STD (100% company paid)
• LTD (100% company paid)
• Generous PTO Package
• 7.5 Paid Holidays
• Flexible Scheduling
• Employee Discounts and Perks
We are an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.

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