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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 ...

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 ...

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 ...

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 ...

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All JobsClinical Trial Associate JobsClinical Trial Associate Jobs in Alabama

Clinical Trial Associate information

See Alabama salary details

$15

$36

$63

How much do clinical trial associate jobs pay per hour?

As of Aug 28, 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 Trials Associate

Worldwide Clinical Trials

Montgomery, AL

$16.83 - $33.65/hr

Full-time

Posted 8 days ago

Job description

Who we are

We're a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world's most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence.

We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs - in the best possible way.

Our mission is to work with passion and purpose every day to improve lives and we are looking for others who value this same pursuit.

Why Worldwide

We believe everyone plays an important role in making a world of difference for patients and their caregivers. From our hands-on, accessible leaders, to our cohesive and supportive teams, we are committed to enabling professionals from all backgrounds and experiences to succeed. We prioritize cultivating a diverse and inclusive environment that continues to promote collaboration and creativity. We are proud to be a workplace where people thrive by being themselves and are inspired to do their best work every day.Join us!

*The Clinical Trials Associate is responsible for providing administrative and project tracking support to the clinical project team, ensuring tasks for all assigned projects with Project Delivery services are performed timely and accurately.**RESPONSIBILITIES:*_Tasks may include but are not limited to:_ Arrange and track system access for project team (Project Managers, Lead CRAs, CRAs, etc.)Maintain and quality audit to assure the most recent revisions of documents are on project portalsAssist project team with preparation and shipment of clinical trial documentation, including Investigator Site FileMaintain version and quality control of project documentation and submit to trial master fileAssist with the tracking and maintenance of project related information, including site medical question and answer logGenerate and distribute minutes for a range of project related meetings, including Sponsor and Internal ManagementMaintain current participating site and personnel informationArrange and track the distribution of project specific training to the project teamPerform other duties as assigned _The responsibilities listed above are representative of the nature and level of work assigned and are not necessarily all-inclusive.__ _*SKILLS AND ABILITIES:* Excellent written and verbal English as well as fluency of the language of the country of location Strong interpersonal skills Ability to work independently and as a team memberSense of urgency and ability to be adaptable in a fast-paced and rapidly changing environmentAbility to handle multiple tasks and exercise independent judgment Strong attention to detail and focus on quality of workStrong organizational and problem-solving skills Excellent skills in MS Office applications including Outlook, Word, Excel and PowerPointKnowledge and understanding of ICH, GCP, and FDA or EU directive regulations (as applicable) *REQUIREMENTS:* Degree level qualification or equivalent experience plus a minimum of one years’ experience in a related roleSkill sets and proven performance equivalent to the above

At Worldwide Clinical Trials, we are committed to fostering an inclusive and equitable workplace by providing transparent compensation.
The salary range for this position is annually (For hourly paid positions, the stated salary range reflects hourly rates):


United States of America - $16.83 - $33.65


The salary range provided is intended to give candidates an understanding of potential earnings. Compensation will fall within the provided range, and it not a guarantee of exact salary. The final salary will be determined based on relevant experience, performance, education, and internal equity. In addition to base salary, we offer a competitive benefits package depending on location. We ensure pay equity and transparency and comply with all applicable labor laws. Salary information will be discussed during the interview process, and we encourage candidates to inquire about compensation at any stage.

We love knowing that someone is going to have a better life because of the work we do.

To view our other roles, check out our careers page at Discover a world of difference at Worldwide!For more information on Worldwide, visit www.Worldwide.com or connect with us on LinkedIn.

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