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Clinical Trial Associate Jobs in Alabama (NOW HIRING)

Becton, Dickinson and Company

Strong understanding of clinical trial operations, monitoring practices, investigational product ... associates through our comprehensive Total Rewards program. We are committed to attracting and ...

Temple University

$120K/yr

The position will require knowledge and utilization of various systems for clinical trial ... Research Associates, Clinical Research Coordinators, Research Specialists, and Research ...

Houston Methodist

... Associate (ACRP) or ACRP-CP - Clinical Research Professional (ACRP) SKILLS AND ABILITIES ... Excellent working knowledge of the clinical trial operations * Ability to identify and/or resolve ...

Tennessee Oncology

... the leading clinical trial networks in the country. Established 1976 in Nashville, Tennessee ... An associate degree in nursing, preferably a bachelor's degree * RN License * 2 years of nursing ...

MSD

... all phases of the trial. * Performs clinical study site management/monitoring activities in ... Associate's degree, certificate or equivalent in a scientific / healthcare discipline together with ...

Merck & Co.

... trial.Performs clinical study site management/monitoring activities in compliance with ICH-GCP ... Associate's degree, certificate or equivalent in a scientific / healthcare discipline together with ...

Merck & Co.

... trial.Performs clinical study site management/monitoring activities in compliance with ICH-GCP ... Associate's degree, certificate or equivalent in a scientific / healthcare discipline together with ...

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Clinical Trial Associate information

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$15

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$63

How much do clinical trial associate jobs pay per hour?

As of Sep 8, 2026, the average hourly pay for clinical trial associate in Alabama is $36.24, according to ZipRecruiter salary data. Most workers in this role earn between $29.18 and $39.86 per hour, depending on experience, location, and employer.

What is a clinical trial associate?

A clinical trial associate helps oversee late-stage drug trials. They design and implement the final clinical study before making reports to the FDA and other regulatory bodies. Their duties cover logistics, including ordering supplies, auditing all reports and documents, and ensuring their timely completion. They are responsible for making sure that the trial follows all ICH and GCP requirements.

What does a clinical trial associate do?

A Clinical Trial Associate (CTA) is responsible for supporting the planning, coordination, and management of clinical trials. They help ensure studies comply with regulatory requirements and assist in maintaining trial documentation, tracking study progress, and communicating with clinical sites. CTAs work closely with clinical research teams, sponsors, and vendors to keep trials running smoothly and efficiently. Their administrative and logistical support is essential for successful clinical research.

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

To thrive as a Clinical Trial Associate, you need a solid understanding of clinical research processes, regulatory guidelines, and a relevant life sciences degree. Familiarity with electronic data capture (EDC) systems, CTMS (Clinical Trial Management Systems), and GCP (Good Clinical Practice) certification are commonly required. Attention to detail, strong organizational skills, and effective communication set top performers apart in this role. These competencies are crucial for ensuring compliance, accurate data management, and smooth coordination of clinical trial activities.

What are some common challenges faced by clinical trial associates when managing study documentation?

Clinical Trial Associates often encounter challenges related to maintaining accurate and up-to-date trial documentation, as protocols and regulatory requirements can change frequently. Ensuring all documents are correctly filed, version-controlled, and accessible for audits requires strong attention to detail and organizational skills. Additionally, coordinating with multiple stakeholders—such as clinical research coordinators, data managers, and regulatory teams—can add complexity to document management. Proactive communication and adopting robust documentation systems can help overcome these challenges.

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

AspectClinical Trial AssociateClinical Research Coordinator
CredentialsBachelor's degree, often in life sciences; certifications like ACRP or SOCRABachelor's degree in health sciences or related field; similar certifications
Work EnvironmentPharmaceutical companies, CROs, clinical trial sitesHospital, academic medical centers, clinical trial sites
ResponsibilitiesAssist in trial setup, data collection, regulatory complianceManage patient recruitment, conduct visits, data entry
Industry UsageCommon in pharmaceutical and biotech industriesCommon in hospitals and academic research settings

Both roles support clinical trials but differ mainly in scope and setting. Clinical Trial Associates typically work in industry settings focusing on trial logistics and compliance, while Clinical Research Coordinators often manage patient interactions and data at clinical sites. Understanding these differences helps in choosing the right career path or job search focus.

More about Clinical Trial Associate jobs

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Clinical Trial Associate jobs near you
Infographic showing various Clinical Trial Associate job openings in Alabama as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $75,384 per year, or $36.2 per hour.

Clinical Research Coordinator (CRC) / RN Clinical Research Coordinator

The US Oncology Network

Mobile, AL • On-site

$20 - $26.50/hr

Full-time

This job post has expired 1 day ago. Applications are no longer accepted.

Key responsibilities

  • Coordinate and manage clinical trial activities, including patient screening, enrollment, and monitoring.

  • Collect, enter, and report study data accurately while ensuring regulatory compliance and documentation.

  • Assist with investigational drug management, including dispensing medications and maintaining accountability.

US Oncology rating

7.1

Company rating: 7.1 out of 10

Based on 109 frontline employees who took The Breakroom Quiz

378th of 898 rated healthcare providers

Job description

Overview

Southern Cancer Center – Springhill Location

Join Our Team!

Southern Cancer Center is seeking a highly organized, detail-oriented, and compassionate Clinical Research Coordinator to join our growing team. This role is critical to advancing cancer care through clinical research by coordinating patient participation in clinical trials and ensuring compliance with study protocols, regulatory requirements, and quality standards.

 
Southern Cancer Center welcomes applications from both Clinical Research Coordinators and Registered Nurses. Qualified RN candidates may be considered for placement in an RN Clinical Research Coordinator role based on education, licensure, and relevant experience.
 

If you are passionate about improving patient outcomes, enjoy working collaboratively with physicians and research teams, and thrive in a fast-paced healthcare environment, we encourage you to apply.

Position Summary

The Clinical Research Coordinator is responsible for coordinating and managing clinical trial activities, including patient screening, enrollment, data collection, regulatory compliance, and ongoing patient monitoring. This individual works closely with physicians, research sponsors, patients, and other healthcare professionals to ensure successful execution of clinical research studies.


Responsibilities
Essential Duties & ResponsibilitiesPatient Recruitment & Clinical Trial Coordination
  • Screen potential patients for protocol eligibility.
  • Present clinical trial opportunities and study details to patients and families.
  • Participate in the informed consent process and enroll eligible patients into clinical trials.
  • Assist with patient care activities required by study protocols.
  • Monitor patient participation and ensure protocol compliance throughout the study.
Clinical Research Activities
  • Collect, enter, and report study data accurately and timely.
  • In collaboration with physicians, review patients for:
    • Changes in condition
    • Adverse events
    • Concomitant medication use
    • Protocol compliance
    • Response to study treatment
  • Thoroughly document all research-related activities and findings.
  • Maintain accurate and complete study records.
Investigational Drug Management
  • May dispense investigational medications in accordance with protocol requirements.
  • Maintain investigational drug accountability and documentation.
Regulatory & Compliance Responsibilities
  • Assist in the collection, preparation, and maintenance of regulatory documents.
  • Ensure compliance with US Oncology Research (USOR) Standard Operating Procedures (SOPs), FDA regulations, and Good Clinical Practice (GCP) guidelines.
  • Participate in monitoring visits, audits, and quality assurance activities.
  • Schedule and coordinate sponsor monitoring and auditing visits as needed.
  • Serve as a liaison with study sponsors, monitors, and auditors.
Laboratory & Specimen Management
  • Assist with collection, preparation, packaging, and shipment of laboratory specimens to central laboratories and vendors.
  • Complete Hazmat and/or IATA training as required.
Professional Development
  • Participate in mandatory training, continuing education, and research-related learning opportunities.
  • Stay current on clinical research regulations, protocols, and best practices.

Qualifications
QualificationsEducation
  • Associate degree in a clinical, scientific, or healthcare-related field required.
  • Bachelor's degree preferred.
Experience
  • Minimum of one (1) year of experience in a clinical or scientific healthcare setting required.
  • Oncology experience strongly preferred.
  • Experience working directly with physicians preferred.
  • Proficiency in Microsoft Office applications required.
Knowledge, Skills & Abilities
  • Excellent verbal and written communication skills.
  • Strong organizational and prioritization skills.
  • Ability to manage multiple tasks and deadlines simultaneously.
  • Exceptional time management skills.
  • Strong interpersonal skills with the ability to work effectively across all levels of the organization.
  • High degree of accuracy and attention to detail.
  • Ability to work independently and collaboratively in a fast-paced environment.
  • Ability to maintain patient confidentiality and professionalism.
  • May be responsible for performing basic clinical assessments.
Why Join Southern Cancer Center?

At Southern Cancer Center, our mission is to provide compassionate, high-quality cancer care while advancing treatment options through innovative clinical research. As a member of our team, you will have the opportunity to make a meaningful impact on patients' lives while contributing to the future of oncology care.

Working ConditionsWork Environment
  • Traditional clinical and office environment.
  • Frequent exposure to conditions common in an oncology/hematology practice, including communicable diseases, toxic substances, ionizing radiation, and medical preparations.
  • Reasonable accommodations may be made to enable qualified individuals with disabilities to perform essential job functions.
Physical Requirements
  • Significant computer-based work.
  • Frequent standing and walking throughout the clinic.
  • Occasional lifting and carrying of items up to 40 pounds.
  • Requires corrected vision and hearing within normal ranges.
Apply Today

Become part of a team dedicated to advancing cancer treatment and improving the lives of our patients through exceptional care and innovative research.

Southern Cancer Center is an Equal Opportunity Employer.

Qualifications:QualificationsEducation
  • Associate degree in a clinical, scientific, or healthcare-related field required.
  • Bachelor's degree preferred.
Experience
  • Minimum of one (1) year of experience in a clinical or scientific healthcare setting required.
  • Oncology experience strongly preferred.
  • Experience working directly with physicians preferred.
  • Proficiency in Microsoft Office applications required.
Knowledge, Skills & Abilities
  • Excellent verbal and written communication skills.
  • Strong organizational and prioritization skills.
  • Ability to manage multiple tasks and deadlines simultaneously.
  • Exceptional time management skills.
  • Strong interpersonal skills with the ability to work effectively across all levels of the organization.
  • High degree of accuracy and attention to detail.
  • Ability to work independently and collaboratively in a fast-paced environment.
  • Ability to maintain patient confidentiality and professionalism.
  • May be responsible for performing basic clinical assessments.
Why Join Southern Cancer Center?

At Southern Cancer Center, our mission is to provide compassionate, high-quality cancer care while advancing treatment options through innovative clinical research. As a member of our team, you will have the opportunity to make a meaningful impact on patients' lives while contributing to the future of oncology care.

Working ConditionsWork Environment
  • Traditional clinical and office environment.
  • Frequent exposure to conditions common in an oncology/hematology practice, including communicable diseases, toxic substances, ionizing radiation, and medical preparations.
  • Reasonable accommodations may be made to enable qualified individuals with disabilities to perform essential job functions.
Physical Requirements
  • Significant computer-based work.
  • Frequent standing and walking throughout the clinic.
  • Occasional lifting and carrying of items up to 40 pounds.
  • Requires corrected vision and hearing within normal ranges.
Apply Today

Become part of a team dedicated to advancing cancer treatment and improving the lives of our patients through exceptional care and innovative research.

Southern Cancer Center is an Equal Opportunity Employer.

Education:UNAVAILABLEEmployment Type: FULL_TIME

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