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Clinical Quality Associate Jobs in Baton Rouge, LA

... the Quality Monitoring of clinic activity. Attend case conferences, staff meetings, and other ... associates and staff. Continuous Improvements: · Continuously looks for and suggests ways to ...

... the Quality Monitoring of clinic activity. Attend case conferences, staff meetings, and other ... associates and staff. Continuous Improvements: · Continuously looks for and suggests ways to ...

... the Quality Monitoring of clinic activity. Attend case conferences, staff meetings, and other ... associates and staff. Continuous Improvements: • Continuously looks for and suggests ways to ...

... the Quality Monitoring of clinic activity. Attend case conferences, staff meetings, and other ... associates and staff. Continuous Improvements: · Continuously looks for and suggests ways to ...

... the Quality Monitoring of clinic activity. Attend case conferences, staff meetings, and other ... associates and staff. Continuous Improvements: • Continuously looks for and suggests ways to ...

... the Quality Monitoring of clinic activity. Attend case conferences, staff meetings, and other ... associates and staff. Continuous Improvements: • Continuously looks for and suggests ways to ...

Candidates with an Associate Degree from a CODA-accredited Dental Hygiene program can enter at this ... Uphold the highest standards of infection control and support clinical quality assurance protocols.

Candidates with an Associate Degree from a CODA-accredited Dental Hygiene program can enter at this ... Uphold the highest standards of infection control and support clinical quality assurance protocols.

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Clinical Quality Associate information

See Baton Rouge, LA salary details

$12

$30

$53

How much do clinical quality associate jobs pay per hour?

As of Sep 3, 2026, the average hourly pay for clinical quality associate in Baton Rouge, LA is $30.29, according to ZipRecruiter salary data. Most workers in this role earn between $20.34 and $39.95 per hour, depending on experience, location, and employer.

What is a clinical quality associate?

Clinical Quality Associates are professionals who support the quality assurance processes within clinical trials or healthcare settings. They are responsible for ensuring that clinical practices comply with regulatory requirements, internal protocols, and industry standards. Their duties often include auditing clinical documents, monitoring study processes, and identifying areas for improvement. By maintaining high-quality standards, Clinical Quality Associates help ensure patient safety and the integrity of clinical data.

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

To thrive as a Clinical Quality Associate, you need a solid understanding of clinical research processes, regulatory compliance, and quality assurance principles, typically supported by a degree in life sciences or a related field. Familiarity with Good Clinical Practice (GCP) guidelines, clinical trial management systems (CTMS), and quality management software is often required. Strong attention to detail, analytical thinking, and effective communication skills make candidates stand out in this role. These skills ensure clinical trials adhere to regulatory standards and deliver reliable, high-quality data for patient safety and successful study outcomes.

What are the main challenges clinical quality associates face when ensuring compliance across multiple clinical trial sites?

Clinical Quality Associates often encounter the challenge of maintaining consistent quality and regulatory compliance across diverse clinical trial sites, each with their own procedures and personnel. Coordinating with site staff, monitoring documentation, and ensuring adherence to Good Clinical Practice (GCP) guidelines require strong communication and organizational skills. Additionally, adapting to frequent regulatory updates and handling discrepancies in real time can be demanding, but these challenges also offer opportunities to develop expertise in quality assurance processes and regulatory requirements.

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

AspectClinical Quality AssociateClinical Research Coordinator
Required CredentialsTypically a bachelor's degree in life sciences or related field; certifications like CQA are a plusBachelor's degree in health sciences, biology, or related field; often requires research-specific certifications
Work EnvironmentQuality assurance departments, regulatory compliance teams, pharmaceutical or biotech companiesClinical trial sites, hospitals, research institutions
Employer & Industry UsageUsed in pharmaceutical, biotech, and healthcare industries focusing on quality and complianceCommon in academic, hospital, and clinical research settings

The Clinical Quality Associate primarily focuses on ensuring compliance with quality standards and regulatory requirements within the industry, while the Clinical Research Coordinator manages the day-to-day operations of clinical trials. Both roles require strong attention to detail and knowledge of clinical processes but differ in their core responsibilities and work environments.

What are the most commonly searched types of Clinical Quality jobs in Baton Rouge, LA?

The most popular types of Clinical Quality jobs in Baton Rouge, LA are:

$103K - $123K/yr

Part-time

Re-posted 12 days ago


Job description

Ensuring Safe, Effective, and Compassionate Medication Management

What We're Looking For:

BS in Pharmacy (required).

Current Louisiana pharmacist license (required).

Hospital pharmacy experience preferred.

Strong knowledge of drug therapy, contraindications, interactions, and USP <797> sterile standards.

Ability to supervise pharmacy technicians and support personnel.

Effective communication, clinical judgment, and problem-solving skills.

Ability to interpret medication orders and collaborate with clinical teams.

Why You'll Love Working With Us:

A collaborative pharmacy team committed to safe, high-quality medication management.

Professional development, CE opportunities, and continued learning.

Mission-centered environment built on service, compassion, and excellence.

Employee perks: https://www.brgeneral.org/about/careers/perks

What You Will Do:

Provide safe, accurate, and cost-effective medication therapy management across the hospital, fulfilling physician orders, monitoring drug therapy, and supporting medication safety.

Prepare and dispense medications according to physician orders and protocols.

Interpret, verify, and document written and electronic medication orders.

Maintain accurate patient medication profiles.

Compound sterile products, chemotherapy, and TPN in accordance with USP <797>.

Issue and document controlled substances per regulations.

Monitor therapies for contraindications, interactions, allergies, and appropriateness.

Review patient charts and document clinical interventions.

Identify and report adverse drug reactions.

Consult with practitioners and recommend cost-effective therapeutic alternatives.

Participate in medication use reviews, audits, and quality improvement activities.

Supervise pharmacy technicians and support personnel.

Perform medication storage inspections and remove outdated medications.

Support pharmacy automation and technology systems.

Collaborate with IS, vendors, Nursing, Billing, and Clinical Informatics.

Maintain licensure, CE documentation, competency requirements, and attend meetings.

Perform all other duties as assigned.

What Sets BRG Apart:

At Baton Rouge General, our pharmacy team plays a vital role in ensuring patients receive safe, effective, and timely care. Our pharmacists drive clinical quality, medication safety, and interdisciplinary collaboration across the hospital. Join a team that values your expertise and dedication.