Top 1 Research coordinator Jobs in Houma La

Research Coordinator
Cardiovascular Institute of the South —Houma, LA
- OSHA
- BLS Certification
- Mid-level
- Profit sharing
- Paid holidays
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5d

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Education-Board of Regents —Chauvin, LA
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Clinical Research Assistant
Tandem Intermediate LLC —Houma, LA
Study Coordination Support: Assist Clinical Research Coordinators in trial-related organization and documentation, including filing and maintaining regulatory…
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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,…
Clinical Research Coordinator I
Nationwide Children's Hospital —Columbus, OH
Recruits, consents and enrolls subjects according to ICH/GCP regulations, and subjects’ rights through institutional IRB, federal and state regulations; answers…

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Research Coordinator

Cardiovascular Institute of the South -
Houma, LA

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Job Details

5 days ago

Benefits

Profit sharing
Paid holidays
Disability insurance
Health insurance
Dental insurance
Employee assistance program
Vision insurance
401(k) matching
Life insurance

Qualifications

High school diploma or GED
Certified Medical Assistant

Full Job Description

Who We Are:

Cardiovascular Institute of the South, a leading organization dedicated to advancing heart health through innovation and excellence, is part of a national cardiology platform, Cardiovascular Logistics (CVL). Together, we share the same mission to provide our patients with the highest quality cardiovascular care available. Join our team and be a part of an organization that is dedicated to improving patient outcomes and shaping the future of heart health.

What We Offer:

Choice of three health insurance plans
Dental insurance coverage
Vision insurance coverage
401(k) with company match and profit-sharing plan
Company-paid short-term and long-term disability coverage
Company-paid life insurance for you and your family
Access to company-provided training and educational resources
Eligibility for annual merit-based performance increases
Accrued General Purpose Time (GPT)
Eight company-paid holidays
Special company events, including Christmas parties, Family Day, employee engagement activities, and Spirit Days
Complimentary Employee Assistance Program (EAP) for all employees and their dependents

About the Role:

Support clinical research studies by coordinating participant recruitment, screening, scheduling, and study visits.
Assist physicians and research nurses in delivering high-quality patient care while ensuring compliance with study protocols, FDA regulations, and Good Clinical Practice (GCP) standards.
Manage study documentation, data collection, laboratory processes, and communication with sponsors, investigators, and regulatory agencies.
Play a key role in maintaining participant safety and contributing to the successful completion of clinical trials.

How You'll Drive Our Mission Forward:

Recruit and engage study participants through community outreach, physician referrals, and screening efforts.
Ensure accurate and timely collection, documentation, and reporting of study data, adverse events, and regulatory requirements.
Coordinate participant visits and maintain ongoing communication to promote a positive study experience and strong retention.
Support regulatory compliance by maintaining study records, preparing for audits and monitoring visits, and collaborating with sponsors and IRBs.
Help advance medical research by contributing to the successful execution and completion of clinical trials.

What Makes You a Great Match:

High School Diploma required
Certified Medical Assistant (CMA) certification required.
Clinical research experience preferred, with an understanding of study coordination, documentation, and regulatory requirements.
Current Basic Life Support (BLS) certification.
Strong organizational skills with the ability to manage multiple priorities and maintain detailed records.
Excellent communication and interpersonal skills, with a commitment to patient care and participant safety.
Team-oriented mindset with a willingness to learn, collaborate, and support colleagues in a fast-paced clinical environment.
Ability to maintain accuracy, confidentiality, and compliance with FDA, OSHA, and study-specific guidelines.

Education

Required

High School or better

Licenses & Certifications

Required

Cert. Clinical Med Asst

Equal Opportunity Employer
This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights (https://www.eeoc.gov/poster) notice from the Department of Labor.

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Research Coordinator

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