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Clinical Research Coordinator Jobs in Decatur, AL

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$14

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$39

How much do clinical research coordinator jobs pay per hour?

As of Aug 25, 2026, the average hourly pay for clinical research coordinator in Decatur, AL is $26.89, according to ZipRecruiter salary data. Most workers in this role earn between $21.88 and $29.09 per hour, depending on experience, location, and employer.

What is a clinical research coordinator?

A Clinical Research Coordinator (CRC) is a professional who manages and oversees clinical trials and research studies involving human participants. They are responsible for ensuring that studies are conducted according to protocol, regulatory requirements, and ethical standards. CRCs handle tasks such as recruiting participants, collecting and managing data, coordinating with research teams, and maintaining documentation. Their work is essential in advancing medical knowledge and ensuring the safety and rights of study participants.

What is a clinical research coordinator?

As a clinical research coordinator, your responsibilities and duties include overseeing research volunteers during medical trials for new drugs and medical devices. You train the volunteers and educate them about the trial and the rules they must follow. You also record data that they report and ensure they are doing the research ethically. Your job is to work with trial subjects, oversee the administration of medication or device usage, and conduct data collection accurately so that the results are as sound as possible. You must also report any unethical practices or concerns regarding trial volunteers to the doctors doing this research.

What are some common challenges faced by clinical research coordinators when managing multiple studies simultaneously?

Clinical Research Coordinators often manage several studies at once, which can present challenges in balancing timelines, documentation, and communication with various stakeholders. Keeping track of regulatory requirements, participant schedules, and data integrity for each study requires strong organizational skills and adaptability. Coordinators frequently collaborate with investigators, sponsors, and clinical staff to ensure protocol adherence and resolve issues quickly, making effective multitasking and prioritization essential to success in this role.

What are the key skills and qualifications needed to thrive as a Clinical Research Coordinator, and why are they important?

To thrive as a Clinical Research Coordinator, you need strong organizational abilities, attention to detail, and knowledge of clinical trial processes, often supported by a degree in life sciences or healthcare. Familiarity with regulatory compliance systems (such as GCP), electronic data capture (EDC) tools, and certifications like ACRP or SOCRA are typically required. Excellent communication, problem-solving, and teamwork skills enable effective coordination among investigators, sponsors, and patients. These competencies are crucial for maintaining data integrity, ensuring regulatory adherence, and supporting the overall success of clinical research studies.

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

AspectClinical Research CoordinatorClinical Research Associate
CredentialsTypically requires a bachelor's degree in health sciences or related field; certifications like CCRP are commonOften requires a bachelor's or master's degree; certifications like CCRP or RAC are advantageous
Work EnvironmentWorks primarily at research sites, hospitals, or clinicsWorks mainly at sponsor offices, CROs, or monitoring sites
Employer & IndustryResearch institutions, hospitals, clinicsPharmaceutical companies, CROs, biotech firms
Job FocusManages daily study activities, patient recruitment, data collectionMonitors study progress, ensures compliance, verifies data accuracy

While both roles support clinical trials, Clinical Research Coordinators handle on-site study management and patient interactions, whereas Clinical Research Associates focus on monitoring and compliance from a remote or office setting. Understanding these differences helps in choosing the right career path or job search focus.

What qualifications do you need to be a clinical research coordinator?

A clinical research coordinator typically needs a bachelor's degree in health sciences, biology, or a related field. Relevant experience in clinical settings, strong organizational skills, and knowledge of Good Clinical Practice (GCP) guidelines are also important; some positions may require certification such as the Certified Clinical Research Coordinator (CCRC).
More about Clinical Research Coordinator jobs

What are the most commonly searched types of Clinical Research jobs in Decatur, AL?

The most popular types of Clinical Research jobs in Decatur, AL are:

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For Clinical Research Coordinator jobs in Decatur, AL, the most frequently searched job titles are:

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The top searched job categories for Clinical Research Coordinator jobs in Decatur, AL are:

What cities near Decatur, AL are hiring for Clinical Research Coordinator jobs?

Cities near Decatur, AL with the most Clinical Research Coordinator job openings:

Clinical Research Coordinator jobs near you
Infographic showing various Clinical Research Coordinator job openings in Decatur, AL as of August 2026, with employment types broken down into 58% Full Time, and 42% Contract. Highlights an 100% In-person job distribution, with an average salary of $55,934 per year, or $26.9 per hour.

CLINICAL RESEARCH COORDINATOR I (HUNTSVILLE)

UAB NOVA RENT

Huntsville, AL • On-site

$43K - $57K/yr

Full-time

Posted 11 days ago

Job description

The University of Alabama at Birmingham (UAB), Huntsville Medical Campus-Research, is seeking a Clinical Research Coordinator I.
The Clinical Research Coordinator I supports a mental health clinical trials clinic. This position will be involved in clinical research studies in patients with serious mental health disorders. This position will interact with other team members and senior investigators. Primary duties include: organizing patient enrollment planning, compiling and analyzing data, maintaining records, tracking progress, and conducting quality assurance on data collected.
General Responsibilities
  • To serve as coordinator for studies and provide support to other team members within the confines of the protocol as directed.
  • To support screening and participant eligibility determination, working with more senior team members to ensure compliance.
  • To conduct activities in accordance with the protocol, regulations and Good Clinical Practice (GCP).
  • To assist with the study life cycle from start-up to closure, i.e., collecting and recording data, recruiting and performing follow-up with participants, scheduling visits, and assisting in coordination of lab and fieldwork.
  • Performs other duties as assigned.

Annual Salary Range : $43,890 - $57,055
Qualifications
High School diploma or GED required.
Preferences
Hard Skills: Experience in clinical trials, placing IVs, and phlebotomy preferred.
Soft Skills: Must have willingness to collect vital signs and handle biological samples (e.g., blood samples), strong verbal and written communication skills, and ability to handle confidential research study data.
UAB is an Equal Employment/Equal Educational Opportunity Institution dedicated to providing equal opportunities and equal access to all individuals regardless of race, color, religion, ethnic or national origin, sex (including pregnancy), genetic information, age, disability, and veteran's status. As required by Title IX, UAB prohibits sex discrimination in any education program or activity that it operates. Individuals may report concerns or questions to UAB's Assistant Vice President and Senior Title IX Coordinator. The Title IX notice of nondiscrimination is located at uab.edu/titleix.

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