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Clinical Operations Associate Jobs in Georgia (NOW HIRING)

Agilent

Sr. Clinical Trials Manager

Turin, GA · On-site

The CTM will report to a Clinical Operations Manager, Senior Manager, or Director,depending on ... Associates (CRAs) to ensure propersite training and management, provide ongoing oversight of ...

Amedisys, Inc.

RN Clinical Manager Home Health

Macon, GA · On-site

$100K/yr

Organizes clinical operations for the care center. * Reviews requests for services and determines ... Associate or bachelor's degree in nursing. * Current RN license, specific to the state(s) you are ...

Amedisys, Inc.

RN Clinical Manager Home Health

Athens, GA · On-site

$20K/yr

Organizes clinical operations for the care center. * Reviews requests for services and determines ... Associate or bachelor's degree in nursing. * Current RN license, specific to the state(s) you are ...

Amedisys, Inc.

RN Clinical Manager Home Health

Tucker, GA · On-site

$20K/yr

Organizes clinical operations for the care center. * Reviews requests for services and determines ... Associate or bachelor's degree in nursing. * Current RN license, specific to the state(s) you are ...

Amedisys, Inc.

RN Clinical Manager Home Health

Athens, GA · On-site

$20K/yr

Organizes clinical operations for the care center. * Reviews requests for services and determines ... Associate or bachelor's degree in nursing. * Current RN license, specific to the state(s) you are ...

Amedisys, Inc.

Clinical Manager Hospice RN

Athens, GA · On-site

Organizes clinical operations for the care center. * Reviews requests for services and determines ... Associate or bachelors degree in nursing. * One year of clinical RN experience in home health or ...

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Clinical Operations Associate information

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How much do clinical operations associate jobs pay per hour?

As of Jun 16, 2026, the average hourly pay for clinical operations associate in Georgia is $22.16, according to ZipRecruiter salary data. Most workers in this role earn between $15.00 and $25.58 per hour, depending on experience, location, and employer.

What is a Clinical Operations Associate job?

A Clinical Operations Associate supports the planning, execution, and management of clinical trials to ensure compliance with regulatory guidelines and company protocols. They assist in coordinating trial logistics, managing documentation, and communicating with study sites and stakeholders. Their role helps ensure studies run efficiently, meet regulatory requirements, and generate reliable data for drug development and approvals.

What do we mean by clinical?

In the context of a Clinical Operations Associate role, 'clinical' refers to activities related to the development, management, and oversight of clinical trials involving human participants. This includes tasks such as protocol adherence, data collection, and ensuring compliance with regulatory standards like GCP and FDA requirements.

What does very clinical mean?

In the context of a Clinical Operations Associate role, 'very clinical' typically refers to a work environment that is highly focused on medical, scientific, and regulatory aspects of clinical trials. It involves detailed knowledge of protocols, patient safety, and compliance with industry standards, often requiring familiarity with clinical software and certifications. This environment emphasizes precision, documentation, and adherence to strict procedures.

What are the key skills and qualifications needed to thrive in the Clinical Operations Associate position, and why are they important?

To thrive as a Clinical Operations Associate, you need a solid background in clinical research processes, project management, and regulatory compliance, often supported by a degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and Good Clinical Practice (GCP) certification is highly valued. Attention to detail, strong organizational skills, and effective communication are important soft skills that help manage complex studies and collaborate with cross-functional teams. These abilities are crucial for ensuring that clinical trials run smoothly, meet regulatory standards, and maintain participant safety.

What are the typical responsibilities and team dynamics for a Clinical Operations Associate?

As a Clinical Operations Associate, your typical responsibilities include coordinating study activities, maintaining trial documentation, supporting regulatory submissions, and ensuring adherence to protocols and timelines. You will often work as part of a multi-disciplinary team that includes clinical research coordinators, data managers, and study monitors, frequently communicating with internal and external stakeholders to keep the study on track. Collaboration and adaptability are key, as priorities can shift based on site needs or regulatory updates. This role offers valuable exposure to the operations side of clinical research and can serve as a springboard to more senior roles such as Clinical Project Manager or Clinical Research Associate.

What does it mean for someone to be clinical?

In the context of a Clinical Operations Associate, being clinical refers to working within healthcare or medical research environments, often involving tasks related to patient interactions, clinical trials, or medical data management. It requires understanding clinical protocols, regulatory requirements, and often involves collaboration with healthcare professionals and adherence to safety standards.

What is the movie clinical about?

There is no widely known movie titled 'Clinical.' If referring to a film with that name, it typically involves themes related to medical or psychological clinical settings. For job roles like Clinical Operations Associate, understanding medical or clinical environments can be relevant, but the question appears unrelated to the job itself.
What are the most commonly searched types of Clinical Operations jobs in Georgia? The most popular types of Clinical Operations jobs in Georgia are:
What are popular job titles related to Clinical Operations Associate jobs in Georgia? For Clinical Operations Associate jobs in Georgia, the most frequently searched job titles are:
What job categories do people searching Clinical Operations Associate jobs in Georgia look for? The top searched job categories for Clinical Operations Associate jobs in Georgia are:
What cities in Georgia are hiring for Clinical Operations Associate jobs? Cities in Georgia with the most Clinical Operations Associate job openings:
Clinical Operations Associate jobs near you
RN CLINICAL RESEARCH NURSE COORDINATOR III

RN CLINICAL RESEARCH NURSE COORDINATOR III

Atlanta Diabetes Associates

Atlanta, GA • On-site

$65K - $82K/yr

Full-time

Posted 23 days ago

Job description

Description:

Job Title: RN Clinical Research Nurse Coordinator III


We are seeking a highly skilled and experienced Registered Nurse Clinical Coordinator III to join our team. The successful candidate will be responsible for coordinating and overseeing the clinical operations of our healthcare facility.


Responsibilities:

- Coordinate and oversee the clinical operations of the healthcare facility

- Develop and implement policies and procedures to ensure high-quality patient care

- Provide leadership and guidance to nursing staff

- Collaborate with physicians and other healthcare professionals to ensure effective patient care

- Monitor patient outcomes and implement quality improvement initiatives

- Ensure compliance with regulatory requirements and standards of care

- Participate in the recruitment, training, and evaluation of nursing staff

- Maintain accurate and complete patient records

- Provide patient education and support


Requirements:

- Active Registered Nurse license

- Bachelor's degree in Nursing or related field

- Strong communication and interpersonal skills

- Ability to work collaboratively with healthcare professionals

- Knowledge of regulatory requirements and standards of care

- Excellent problem-solving and critical-thinking skills

- Ability to prioritize and manage multiple tasks


If you are a highly motivated and experienced Registered Nurse Clinical Coordinator III, we encourage you to apply for this exciting opportunity. We offer competitive compensation and benefits packages, as well as opportunities for professional growth and development.

Requirements:

WORKING CONDITIONS

  • Job Type: Full-time (40 hr./week)
  • Location: In office (non-remote)
  • Schedule: Typically follows business hours of 8a-5p, Monday through Friday. Start-End times may vary depending on assigned projects. Occasional weekend and night work required, as assigned by Department manager and/or Research Director.
  • Physical requirements: Must be able to perform tasks as listed on Physical Requirement Checklist.

The above statements are intended to describe the general nature and level of work performed by people assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills required of personnel so classified. Management retains the right to add or to change the duties of the position at any time.


SKILLS AND QUALIFICATIONS

  • Proficient in Microsoft Word, Excel, and PowerPoint applications and general use of computers.
  • High personal motivation, self-management, and detail-orientation; ability to take responsibility in meeting deadlines and making progress without direct supervision.
  • Strong spoken and written communications skills.
  • Must be flexible and adaptable as work conditions, responsibilities and work environment are unpredictable and change frequently
  • Capacity and will to learn new software, research methods, and work routines quickly; flexibility in responding to new research opportunities as they arise.
  • Motivation to engage in and manage a wide range of intellectual and physical work, ranging from preparing mass mailings to analyzing proposed data-collection designs.
  • Strong existing computer skills with Microsoft Office statistical software, and general Internet and electronic communications.
  • Articulate and tactful communications skills; readiness to meet and work directly with clients.
  • Maintain patient, team, and employer confidentiality. Comply with all HIPAA regulations
  • Proven competency in use of medical and laboratory equipment, including maintenance, and protocols.

EDUCATION/EXPERIENCE

  • RN License, or higher required
  • Certified Clinical Research Coordinator preferred