Top 5 Research coordinator Jobs in Covington La

Clinical Research Coordinator
Paradigm Health System —Slidell, LA
- Full-time
- Background check
- Mid-level
- Bachelor's degree
- Health insurance
- Dental insurance
Quick Apply
7d
Clinical Research Coordinator
DelRicht Research —Slidell, LA
- Full-time
- HIPAA
- Clinic
- Bachelor's degree
- Profit sharing
- Disability insurance
Clinical Quality Coordinator
DelRicht Research —Mandeville, LA
- Day shift
- Bachelor of Science
- Mid-level
- Office
- Profit sharing
- Health insurance
Healthcare Project Coordinator
DelRicht Research —Slidell, LA
- Full-time
- Mid-level
- Administrative experience
- Clinic
- Profit sharing
- Disability insurance

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Clinical Research Coordinator
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Bachelor's degree in science, healthcare, or a related field, or equivalent clinical research experience. Clinical Research Coordinator certification (CCRC,…
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Clinical Research Coordinator

Paradigm Health System
Slidell, LA

Quick Apply

Job Details

Full-time
7 days ago

Benefits

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

Qualifications

Teamwork
Electronic health records (EHR) management
Research ethical considerations
Research project coordination
ICH guidelines
Bachelor's degree
Attention to detail
Data entry
Research regulatory compliance
Productivity software
Clinical quality assurance standards
FDA regulations

Full Job Description

About Paradigm Health System:

Paradigm Health System is a premier healthcare provider dedicated to delivering exceptional patient care while driving operational excellence.

Job Summary:

The Clinical Research Coordinator (CRC) is responsible for the day-to-day management and execution of assigned clinical research studies conducted at Paradigm Health System. The CRC works collaboratively with investigators, sponsors, contract research organizations (CROs), and clinical staff to ensure studies are conducted safely, efficiently, and in accordance with study protocols, Good Clinical Practice (GCP), and all applicable regulatory requirements.

The CRC independently coordinates all phases of assigned clinical trials, including participant recruitment, screening, enrollment, study visits, data collection, regulatory documentation, and study closeout. The coordinator serves as the primary point of contact for study participants while ensuring an exceptional patient experience and maintaining the highest standards of research, quality and compliance.

Responsibilities:

Study Coordination

Independently manage assigned clinical research studies from site activation through study closeout
Recruit, screen, consent, enroll, and retain study participants in accordance with protocol requirements
Coordinate and conduct study visits, assessments, laboratory testing, and follow-up activities
Educate participants regarding study procedures, schedules, investigational products, and study expectations
Maintain protocol compliance while promoting participant safety and data integrity

Regulatory & Compliance

Maintain complete, accurate, and contemporaneous source documentation
Prepare and maintain regulatory files and essential study documentation
Ensure compliance with study protocols, ICH-GCP guidelines, FDA regulations, sponsor requirements, and institutional policies
Identify, document, and report protocol deviations, adverse events, and other reportable events as required

Data & Study Management

Collect, review, and enter study data accurately and within sponsor timelines
Resolve sponsor and CRO data queries in a timely manner
Prepare studies for monitoring visits, audits, and inspections
Maintain study supplies, investigational product accountability, and essential study materials
Assist with study financial tracking by documenting completed research procedures and supporting accurate research billing processes

Collaboration

Serve as the primary liaison between participants, investigators, sponsors, CROs, and clinic staff
Participate in site qualification, initiation, monitoring, and closeout visits
Communicate study progress, enrollment updates, and operational issues to the Director of Research
Foster collaborative relationships that support successful study execution across all participating departments

Other

· Responsibilities may be added or modified as organizational and operational needs evolve

Qualifications:

Required

· Bachelor's degree in science, healthcare, or a related field, or equivalent clinical research experience

· Excellent organizational, communication, and interpersonal skills

· Strong attention to detail and commitment to quality

· Ability to independently prioritize workload while managing multiple active clinical trials

· Proficiency with electronic medical records and Microsoft Office applications

· Knowledge of ICH-GCP guidelines, FDA regulations, and human subject protection requirements

· Experience with electronic data capture (EDC) systems and sponsor/CRO interactions

Preferred

· Two or more years of clinical research coordination experience

· Clinical Research Coordinator certification (CCRC, CCRP, or equivalent)

Benefits:

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

Work Location: In person

Quick Apply

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research coordinator jobs in covington la

Clinical Research Coordinator

Clinical Research Coordinator

Clinical Quality Coordinator

Healthcare Project Coordinator

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