Research Coordinator Jobs in Alabama
Research Coordinator jobs in Alabama are concentrated in Birmingham, Huntsville, and Mobile, where academic medical centers, federal contractors, and pharmaceutical firms drive steady demand for coordinators with backgrounds in clinical trials, biomedical research, and defense-related science programs. UAB Medicine, HudsonAlpha Institute for Biotechnology, and Huntsville Hospital are among the anchor employers with long-running research programs that hire at multiple levels, from entry-level associates to senior protocol managers. Clinical trials coordination and federally funded research administration are the most consistently sought specialties across the state. Scan the live roles below and apply to whichever ones fit.
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Showing 5 of 35+ Research Coordinator jobs
The University of Alabama at Birmingham (UAB), O'Neal Comprehensive Cancer Center, is seeking a Clinical Research Nurse Coordinator III.
The O'Neal Comprehensive Cancer Center is one of 51 NCI-designated comprehensive cancer centers in the United States and is the only one in Alabama and in the Deep South region. A comprehensive designation also means UAB Medicine patients have access to leading-edge treatments or clinical trials that they may not otherwise have at local community hospitals or smaller cancer centers. For many, an NCI designation can hold the key to survival. On campus and around Birmingham, the O'Neal Cancer Center is a significant part of our economic powerhouse. The O'Neal Cancer Center powers more than 400 scientists and physician-scientists, cares for 20,000 patients annually, and is home to more than 160 employees, plus all the physicians and clinical staff engaged in cancer patient care. The link to our website is: https://www.uab.edu/onealcancercenter/
Please attach a current resume with this application.
General Responsibilities
To serve as primary coordinator for clinical research studies and supporting more senior team members.
To provide a lead role in protocol screening and participant eligibility determination working alongside other team members to ensure compliance.
To provide oversight to junior clinical research coordinators (CRC) and clinical research nurse coordinators (CRNC) in review of study documents.
To conduct all study activities in accordance with the protocol, Institutional Review Board (IRB) regulations, and Good Clinical Practice (GCP).
To provide quality care to participants and their families within the area of clinical specialty.
To coordinate the life cycle of the study from start-up through maintenance to closure.
To manage participant care including recruitment, screening, scheduling, consenting, conducting visits, and collecting various assessments such as adverse event (AE) information or questionnaires.
To perform the informed consent process following GCP.
To act as a liaison between the clinical and research staff, departments, ancillary services and the study sponsor to ensure protocol compliance throughout a study.
Key Duties & Responsibilities
Conducts and fully understands all study activities, including more complex protocols, IRB regulations, and Good Clinical Practice (GCP). Develops or provides input for IRB documents.
Manages the life cycle of clinical research studies from feasibility to start-up through maintenance to closure. Manages participant care, including recruitment, screening, scheduling, consenting, conducting visits, and collecting various assessments such as adverse event (AE) information or questionnaires. Documents and reviews medical history to determine compliance with eligibility requirements. Develops/prepares study source documentation. Performs the informed consent process following GCP.
Performs clinical procedures as required by the protocol. Prepares for and participates in study monitoring visits and corrects and reports findings as needed.
Serves as a resource person or acts as a subject matter expert (SME) within the area of clinical expertise. Maintains clinical records and documentation, including those associated with compliant billing practices.
Develops study source documentation. Assists with the development of protocols.
Assists colleagues in identifying inefficiencies and improving processes. Mentors and trains junior staff as needed.
Coordinates management of investigational products (IP). May design best practices for management of IP for drug, device, and biologic studies. Creates study budgets as needed. Stays familiar with institutional financial systems.
Maintains a working nursing knowledge of the department specialty, drafts documents or policies, collects records, and prepares data for publication, if needed. May perform general nursing duties.
Performs other duties as assigned.
Annual Salary Range: $67,070 - $108,990
Preferences
Strongly prefer Oncology and/or Clinical Research experience, coordinating research activities involved in conducting Oncology clinical trials.
Management of data and of the study patients' care.
Knowledge of regulatory/compliance affairs as it pertains to clinical research.
Knowledge of protocol financial functions.
Experience in training and mentoring clinical research nurses.
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.
The University of Alabama at Birmingham (UAB), O'Neal Comprehensive Cancer Center, is seeking a Clinical Research Nurse Coordinator III.
The O'Neal Comprehensive Cancer Center is one of 51 NCI-designated comprehensive cancer centers in the United States and is the only one in Alabama and in the Deep South region. A comprehensive designation also means UAB Medicine patients have access to leading-edge treatments or clinical trials that they may not otherwise have at local community hospitals or smaller cancer centers. For many, an NCI designation can hold the key to survival. On campus and around Birmingham, the O'Neal Cancer Center is a significant part of our economic powerhouse. The O'Neal Cancer Center powers more than 400 scientists and physician-scientists, cares for 20,000 patients annually, and is home to more than 160 employees, plus all the physicians and clinical staff engaged in cancer patient care. The link to our website is: https://www.uab.edu/onealcancercenter/
Please attach a current resume with this application.
General Responsibilities
To serve as primary coordinator for clinical research studies and supporting more senior team members.
To provide a lead role in protocol screening and participant eligibility determination working alongside other team members to ensure compliance.
To provide oversight to junior clinical research coordinators (CRC) and clinical research nurse coordinators (CRNC) in review of study documents.
To conduct all study activities in accordance with the protocol, Institutional Review Board (IRB) regulations, and Good Clinical Practice (GCP).
To provide quality care to participants and their families within the area of clinical specialty.
To coordinate the life cycle of the study from start-up through maintenance to closure.
To manage participant care including recruitment, screening, scheduling, consenting, conducting visits, and collecting various assessments such as adverse event (AE) information or questionnaires.
To perform the informed consent process following GCP.
To act as a liaison between the clinical and research staff, departments, ancillary services and the study sponsor to ensure protocol compliance throughout a study.
Key Duties & Responsibilities
Conducts and fully understands all study activities, including more complex protocols, IRB regulations, and Good Clinical Practice (GCP). Develops or provides input for IRB documents.
Manages the life cycle of clinical research studies from feasibility to start-up through maintenance to closure. Manages participant care, including recruitment, screening, scheduling, consenting, conducting visits, and collecting various assessments such as adverse event (AE) information or questionnaires. Documents and reviews medical history to determine compliance with eligibility requirements. Develops/prepares study source documentation. Performs the informed consent process following GCP.
Performs clinical procedures as required by the protocol. Prepares for and participates in study monitoring visits and corrects and reports findings as needed.
Serves as a resource person or acts as a subject matter expert (SME) within the area of clinical expertise. Maintains clinical records and documentation, including those associated with compliant billing practices.
Develops study source documentation. Assists with the development of protocols.
Assists colleagues in identifying inefficiencies and improving processes. Mentors and trains junior staff as needed.
Coordinates management of investigational products (IP). May design best practices for management of IP for drug, device, and biologic studies. Creates study budgets as needed. Stays familiar with institutional financial systems.
Maintains a working nursing knowledge of the department specialty, drafts documents or policies, collects records, and prepares data for publication, if needed. May perform general nursing duties.
Performs other duties as assigned.
Annual Salary Range: $67,070 - $108,990
Preferences
Strongly prefer Oncology and/or Clinical Research experience, coordinating research activities involved in conducting Oncology clinical trials.
Management of data and of the study patients' care.
Knowledge of regulatory/compliance affairs as it pertains to clinical research.
Knowledge of protocol financial functions.
Experience in training and mentoring clinical research nurses.
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.
See All 35 Research Coordinator Jobs in Alabama
Find roles in Alabama that match your experience and apply in just a few clicks.
Find Research Coordinator JobsResearch Coordinator Jobs by City in Alabama
Where Alabama roles are concentrated, by current openings.
Research Coordinator Job Market in Alabama
A snapshot from current Alabama openings, updated as new roles post.
Who's Hiring
- University of Alabama, Birmingham26
- AMR Clinical2
- Alabama Oncology1
- INFIRMARY HEALTH1
- CUNNINGHAM PATHOLOGY1
Top Industries Hiring
- Education
- Healthcare & Medical Services
What Alabama Employers Look For
The qualifications that appear most often in research coordinator jobs across Alabama.
- Bachelor's degree in a life science, public health, or related field required
- Experience with IRB submissions and human subjects research compliance protocols
- Familiarity with GCP guidelines and clinical trial regulatory documentation standards
- Proficiency in research data management systems such as REDCap or similar platforms
- Strong written communication skills for preparing study reports and sponsor correspondence
- Ability to coordinate across multidisciplinary teams in a fast-paced research environment
Research Coordinator Jobs in Alabama: Frequently Asked Questions
How do you become a research coordinator in Alabama?
Most research coordinator positions in Alabama require at minimum a bachelor's degree in a life science, health-related field, or social science, though clinical roles at academic medical centers often prefer candidates with some hands-on lab or patient-facing experience. Alabama does not issue a state-specific license for research coordinators, but many employers prioritize candidates who hold or are working toward the Certified Clinical Research Coordinator credential offered by the Association of Clinical Research Professionals. Gaining experience through UAB, Auburn University research programs, or hospital-based internships is the most reliable entry path.
Which companies hire research coordinators in Alabama?
Alabama research coordinator roles are posted by University of Alabama, Birmingham, AMR Clinical, and Alabama Oncology and others right now, based on current listings on Migrate Mate as of July 2026. Alabama's combination of academic medical institutions, federal defense research in Huntsville, and growing biotech presence means openings appear across multiple sectors rather than clustering in a single industry.
Which Alabama cities have the most research coordinator jobs?
Birmingham, Mobile, and Daphne are the Alabama cities with the most research coordinator openings. Birmingham leads because of UAB Medicine and its extensive clinical trials infrastructure, Huntsville draws openings tied to federal defense and science contractors at the Cummings Research Park, and Mobile adds volume through the University of South Alabama and regional hospital research departments.
Are there remote research coordinator jobs in Alabama?
Yes, but they're rare. Research coordinators often need to be on-site to interact with study participants, manage specimens, and oversee protocol compliance directly. About 40% of research coordinator openings tied to Alabama are remote or hybrid as of July 2026, and those tend to be administrative or data-focused positions rather than hands-on clinical trial roles. Regulatory affairs, data management, and grant coordination are the sub-areas most likely to offer remote flexibility.
How can I get hired as a research coordinator in Alabama with little or no experience?
The most realistic entry path is applying for research assistant or clinical trials assistant roles at UAB's research departments or the HudsonAlpha Institute for Biotechnology, both of which regularly bring on junior staff to support active studies. Hospital systems such as Huntsville Hospital and USA Health also post entry-level coordinator associate roles that do not require prior coordination experience. Adjacent roles like medical assistant, lab technician, or patient services representative at a research site can open the door quickly. Completing a Good Clinical Practice training certification before applying gives candidates a concrete edge over others without prior research exposure.
Where can I find and apply to research coordinator jobs in Alabama?
You can find and apply to research coordinator jobs in Alabama on Migrate Mate, which lists current Alabama openings across clinical, academic, and industry research settings. Search the available roles, identify the ones that match your experience and location, and apply directly to the positions that fit.
See All 35 Research Coordinator Jobs in Alabama
Find roles in Alabama that match your experience and apply in just a few clicks.
Find Research Coordinator Jobs