Top 7 Clinical research coordinator Jobs in Madison, Al

Clinical Research Coordinator - Industry Based
New Horizon Research Group, Inc —Athens, AL
- Full-time
- Background check
- Patient monitoring
- HIPAA
- Health insurance
- Dental insurance
Quick Apply
Clinical Research Assistant
Medovation Clinical Research LLC —Huntsville, AL
- $20 an hour
- Full-time
- Bachelor's degree
- Computer skills
- Communication skills
- Opportunities for advancement
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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
Clinical Donation Coordinator I - PeeDee Region
WE ARE SHARING HOPE SC —United States
- On call
- Mid-level
- Operating room
- 2 years

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Clinical Research Assistant
Medovation Clinical Research LLC —Huntsville, AL
Assist research coordinators and investigators with clinical trial visits. Collect and accurately document clinical research data. Full-Time | Huntsville, AL.
$20 an hour
Quick Apply
Clinical Research Coordinator - Industry Based
New Horizon Research Group, Inc —Athens, AL
Clinical research certification (CCRC, CCRP, or equivalent) preferred. Current *ICH-GCP certification* required.
Quick Apply

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While the DCE retains responsibility for academic oversight, curricular alignment, site development strategy, and clinical decision-making, the CEC provides the…
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Clinical Research Coordinator
OhioHealth —Columbus, OH
This position performs basic day to day activities related to clinical research studies including recruit and screen participants, obtains informed consent,…

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Clinical Research Coordinator - Industry Based

New Horizon Research Group, Inc
Athens, AL

Quick Apply

Job Details

Full-time

Benefits

Health insurance
Dental insurance
Paid time off
Vision insurance

Qualifications

Statistical software
Teamwork
Clinical research
Patient monitoring
IATA Dangerous Goods Certification
HIPAA
Laboratory experience
Phlebotomy specimen handling
Research project coordination
Schedule management
ICH guidelines
Attention to detail
Good Clinical Practice (GCP)
Pharmaceutical research experience
Medical terminology

Full Job Description

Clinical Research Coordinator – Industry-Sponsored Trials

We are seeking a highly organized and detail-oriented Clinical Research Coordinator (CRC) to join our growing clinical operations team. This role is ideal for a research professional with experience in industry-sponsored clinical trials involving pharmaceutical, biotechnology, and medical device studies.

As the CRC, you will coordinate and manage all aspects of clinical trial execution, ensuring compliance with regulatory requirements, sponsor expectations, and study timelines. You will work closely with investigators, staff, Clinical Research Associates (CRAs), sponsors, and study participants to support the successful delivery of high-quality clinical research. This position offers an excellent opportunity to contribute to innovative medical advancements while further developing your clinical research career in a collaborative and fast-paced environment.

Clinical Trial Coordination

Coordinate and oversee all phases of clinical trials, including study start-up, participant recruitment, enrollment, follow-up, and close-out activities.
Conduct protocol feasibility assessments and assist with site initiation.
Ensure studies are conducted in compliance with FDA regulations, ICH-GCP guidelines, HIPAA requirements, sponsor protocols, and institutional policies.

Participant Management

Recruit, screen, enroll, and consent study participants according to protocol requirements.
Schedule and coordinate study visits while ensuring participant safety and protocol adherence.
Perform clinical assessments, including vital signs, specimen collection, and phlebotomy as required by study protocols.
Maintain positive relationships with participants and provide ongoing education throughout the study process.

Data & Documentation Management

Accurately collect, review, and enter clinical trial data into Electronic Data Capture (EDC) systems within sponsor-required timelines.
Verify source documentation, informed consent forms, and study records for completeness and accuracy.
Manage and maintain essential study documents, delegation logs, and electronic Trial Master Files (eTMFs).
Proactively address and resolve data queries from sponsors, monitors, and data management teams.

Site Monitoring & Sponsor Engagement

Serve as a primary point of contact for sponsors, CRAs, and external study partners.
Host site initiation, interim monitoring, audit, and close-out visits.
Support source data verification activities and ensure readiness for inspections and audits.
Communicate study progress, enrollment metrics, and operational updates to sponsors and investigators.

Safety & Compliance

Identify, document, and report Adverse Events (AEs) and Serious Adverse Events (SAEs) in accordance with protocol and regulatory timelines.
Ensure participant confidentiality and data integrity at all times.
Support quality assurance initiatives and maintain inspection-ready study records.

Cross-Functional Collaboration

Collaborate with investigators, research staff, laboratory personnel, and sponsors to achieve study objectives.
Manage multiple clinical trials across diverse therapeutic areas while maintaining high standards of accuracy and efficiency.
Assist with resource planning and operational workflow improvements.

Required Experience

Minimum of 2–3 years of clinical research coordination experience, preferably managing industry-sponsored clinical trials.
Experience working across multiple therapeutic areas preferred.
Demonstrated ability to manage study timelines, participant recruitment, sponsor communications.

Technical Knowledge & Skills

Strong understanding of clinical research regulations, including FDA, ICH-GCP, HIPAA, and applicable compliance requirements.
Proficiency with Electronic Data Capture (EDC) systems such as Medidata Rave, Veeva, Oracle Clinical, or similar platforms.
Experience with eTMF management, EMR systems, and clinical research documentation practices.
Knowledge of medical terminology and clinical development processes.
Proficiency in Microsoft Office Suite and research data management systems.

Clinical Skills

Experience performing phlebotomy, specimen processing, vital signs collection, and other protocol-required clinical procedures.
Ability to review complex clinical documentation with exceptional attention to detail.
Strong organizational, problem-solving, and time-management skills.

Certifications

Current ICH-GCP certification required.
Clinical research certification (CCRC, CCRP, or equivalent) preferred.

Why Join Us?

This is an exciting opportunity to play a key role in advancing innovative therapies and medical technologies. We are looking for motivated professionals who thrive in a fast-paced research environment and are committed to excellence in clinical trial execution, patient safety, and data quality. Join our team and make a meaningful impact on the future of healthcare.

Benefits:

Dental insurance
Health insurance
Paid time off
Vision insurance

Application Question(s):

Do you have industry-based experience as a Clinical Research Coordinator?

Work Location: In person

Quick Apply

Refine Your Search

clinical research coordinator jobs in madison, al

Clinical Research Coordinator - Industry Based

Clinical Research Assistant

Research Coordinator

Research Assistant Professor & FPIC Coordinator

Clinical Donation Coordinator I - PeeDee Region

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