Top 2 Research coordinator Jobs in Huntsville Al

Research Coordinator
Rehabilitation and Neurological Service, LLC —Huntsville, AL
- $15 - $20 an hour
- Full-time
- Bilingual
- Medical office experience
- Mid-level
- Health insurance
- Dental insurance
Quick Apply
Research Assistant Professor & FPIC Coordinator
Alabama A&M University —Normal, AL
- $53,325 - $71,100 a year
- Full-time
- Maintenance
- University
- Doctor of Philosophy
- Disability insurance
- Health insurance

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Research Coordinator

Rehabilitation and Neurological Service, LLC
Huntsville, AL

Quick Apply

Job Details

Full-time
$15 - $20 an hour

Benefits

Health insurance
Dental insurance
401(k)
Paid time off
Vision insurance
401(k) matching

Qualifications

Bilingual
Community engagement experience
Informed consent
Psychiatry
Adverse event reporting
Clinical incident reports
Medical office experience
Regulatory compliance
Phlebotomy specimen handling
Mid-level
Patient safety
Medical scheduling
Research project coordination
Clinical data entry
Clinical information systems
Informed consent procedures implementation
Clinical research inspection readiness
Internal medicine
Patient interaction
Neurology
Productivity software
Documentation Handling
Clinical trial support in drug product development
Pharmaceutical research experience
Communication skills
Quality data entry
Research compliance quality assurance records management

Full Job Description

Benefits:

401(k)
401(k) matching
Dental insurance
Health insurance
Paid time off
Vision insurance

Research Coordinator – Clinical Trials

Rehabilitation & Neurological Services, LLC is seeking an experienced, organized, dependable, and motivated Clinical Research Coordinator to join our growing clinical research team. We are looking for a reliable professional who wants to grow with our organization long-term and become an integral part of a fast-paced, patient-centered research program.

This position requires someone who can work independently, prioritize responsibilities effectively, problem-solve proactively, and maintain professionalism while managing multiple clinical trials and deadlines.

Qualifications

Minimum of 2–3 years of CLINICAL RESEARCH experience preferred
Current GCP (Good Clinical Practice) training/certification required
Medical office, nursing, allied health, or healthcare experience strongly preferred
Prior experience coordinating pharmaceutical and/or device clinical trials
Strong organizational, communication, and multitasking skills
Ability to prioritize and manage multiple studies simultaneously
Dependable, detail-oriented, and self-motivated
Ability to work independently with minimal supervision
Comfortable interacting with patients, sponsors, CROs, physicians, and monitors
Proficiency with EMR systems, Microsoft Office, and electronic data entry systems
Knowledge of IRB processes, informed consent, source documentation, adverse event reporting, and regulatory compliance
Experience with recruitment, retention, and participant scheduling preferred
Phlebotomy experience is a plus
Bilingual candidates are encouraged to apply

Responsibilities

Coordinate and manage day-to-day clinical trial activities
Screen, recruit, and retain study participants
Conduct and document informed consent procedures
Schedule and coordinate study visits and follow-up appointments
Ensure protocol compliance and participant safety
Maintain accurate source documentation, regulatory binders, and study records
Enter and resolve data queries in electronic data capture systems
Communicate effectively with sponsors, CROs, monitors, investigators, and participants
Prepare for sponsor monitoring visits, audits, and site initiation visits
Assist with lab processing, specimen handling, shipping, and study-related procedures
Track enrollment goals, study timelines, visit windows, and regulatory deadlines
Participate in occasional weekend community engagement and outreach events related to research and education
Support a positive, professional, team-oriented environment focused on excellence and growth

Application Requirements

Qualified applicants must submit:

Current resume/CV
List of clinical trials previously worked on
Specific role/capacity on each study (Coordinator, Regulatory, Recruitment, Data Entry, etc.)
Certifications and GCP training documentation
Professional references

Preferred Therapeutic Experience

Neurology
Migraine/Headache Medicine
Alzheimer’s Disease/Dementia
Psychiatry
Internal Medicine or Primary Care

We are seeking someone reliable, professional, organized, and committed to growing with a physician-led research program focused on innovation, patient care, and advancing clinical science. Competitive compensation will be based on experience and qualifications.

Quick Apply

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research coordinator jobs in huntsville al

Research Coordinator

Research Assistant Professor & FPIC Coordinator

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