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Clinical Project Associate Jobs in Alabama (NOW HIRING)

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Clinical Project Associate information

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$11

$28

$50

How much do clinical project associate jobs pay per hour?

As of Aug 31, 2026, the average hourly pay for clinical project associate in Alabama is $28.59, according to ZipRecruiter salary data. Most workers in this role earn between $19.18 and $37.69 per hour, depending on experience, location, and employer.

What is a clinical project associate?

A Clinical Project Associate (CPA) is a professional who supports the planning, execution, and management of clinical trials in the pharmaceutical, biotechnology, or medical device industries. Their responsibilities often include coordinating study documentation, assisting with regulatory submissions, tracking project timelines, and facilitating communication among study teams. CPAs play a crucial role in ensuring that clinical trials are conducted efficiently, ethically, and in compliance with regulatory standards. They work closely with clinical project managers, research associates, and other team members to help bring new therapies and treatments to market.

What are the typical responsibilities of a clinical project associate?

As a Clinical Project Associate, you will play a vital role in ensuring the smooth execution of clinical trials by handling administrative and logistical tasks. Your responsibilities often include maintaining study documentation, coordinating meetings, tracking project timelines, and supporting communication between internal teams and external partners such as clinical sites and vendors. You may also assist with regulatory submissions and help monitor compliance with study protocols. This position offers excellent exposure to the clinical research process and can be a stepping stone to more advanced roles within clinical operations.

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

To thrive as a Clinical Project Associate, you need a background in life sciences or a related field, attention to detail, and strong organizational skills. Familiarity with clinical trial management systems (CTMS), regulatory documentation, and tools like Microsoft Office is typically required. Excellent communication, teamwork, and time management abilities help professionals excel in supporting project coordination. These skills are crucial for ensuring regulatory compliance, smooth project execution, and effective collaboration within clinical research teams.

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

AspectClinical Project AssociateClinical Research Coordinator
CredentialsBachelor's degree often required; certifications like CCRP beneficialBachelor's degree in health or related field; certifications like CCRP common
Work EnvironmentTypically works with project teams, sponsors, and CROs in clinical trial settingsWorks directly with patients, investigators, and site staff at clinical trial sites
Employer & IndustryPharmaceutical companies, CROs, biotech firmsHospitals, clinics, research sites
Search & Comparison IntentHigh overlap in responsibilities and certificationsSimilar roles but more patient-facing

The Clinical Project Associate primarily supports clinical trial management from a project perspective, working with sponsors and CROs. In contrast, the Clinical Research Coordinator focuses on patient interactions and site management. Both roles require similar educational backgrounds and certifications, but their work environments and daily tasks differ significantly.

What are the most commonly searched types of Clinical Project jobs in Alabama?

The most popular types of Clinical Project jobs in Alabama are:

What are popular job titles related to Clinical Project Associate jobs in Alabama?

For Clinical Project Associate jobs in Alabama, the most frequently searched job titles are:

What job categories do people searching Clinical Project Associate jobs in Alabama look for?

The top searched job categories for Clinical Project Associate jobs in Alabama are:

Clinical Project Associate jobs near you
Infographic showing various Clinical Project Associate job openings in Alabama as of August 2026, with employment types broken down into 2% As Needed, 79% Full Time, 12% Part Time, 1% Temporary, and 6% Contract. Highlights an 85% Physical, 1% Hybrid, and 14% Remote job distribution, with an average salary of $59,462 per year, or $28.6 per hour.

Clinical Trials Associate

Worldwide Clinical Trials

Montgomery, AL • On-site

$16.83 - $33.65/hr

Full-time

Posted 11 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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