Top 2 Research coordinator Jobs in Daytona Beach Fl

Senior Clinical Research Coordinator
Arrow Clinical Trials —Daytona Beach, FL
- $60,000 - $70,000 a year
- Full-time
- Background check
- Nursing
- Bachelor of Science
- Health insurance
- Dental insurance
Quick Apply
Oncology Research Coordinator
Halifax Health —Daytona Beach, FL
- Full-time
- Hospital
- Customer service
- Writing skills
2d

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Oncology Research Coordinator
Halifax Health —Daytona Beach, FL
Professional clinical research and/or oncology certification (through SOCRA, ACRP, ONS, etc.) are preferred. Clinical Trial regulatory certification preferred.
2d
Clinical Research Coordinator II RN Oncology
AdventHealth Orlando Support —Altamonte Springs, FL
Maintains clinical competencies including physical assessment, phlebotomy, and IV insertion. Demonstrated skills in clinical competencies including physical…
$65,582.40 - $108,646.85 a year

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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,…
Research Coordinator/Interventionist-1
Nationwide Children's Hospital —Columbus, OH
Valid Ohio driver’s license and proof of auto insurance is required by hospital policy. Degree in social science, health or behavioral field, preferred.

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Senior Clinical Research Coordinator

Arrow Clinical Trials
Daytona Beach, FL

Quick Apply

Job Details

Full-time
$60,000 - $70,000 a year

Benefits

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

Qualifications

Teamwork
Clinical research
Bachelor of Science
HIPAA
Research
GDPR compliance expertise
ICH guidelines
Compliance management
Attention to detail

Full Job Description

Job Summary
We are seeking a highly motivated and detail-oriented Senior Clinical Research Coordinator to lead and manage complex clinical trials across diverse therapeutic areas. In this pivotal role, you will oversee the entire research process, ensuring compliance with regulatory standards, maintaining meticulous documentation, and coordinating with multidisciplinary teams. Your expertise will drive the successful execution of clinical studies, contribute to advancing medical knowledge, and improve patient outcomes. This position offers an exciting opportunity for experienced professionals passionate about clinical research to make a meaningful impact in healthcare innovation.

Duties

Lead the planning, initiation, and management of clinical trials, ensuring adherence to protocols, FDA regulations, ICH GCP standards, and institutional policies.
Supervise and mentor junior staff and research coordinators, fostering a collaborative team environment focused on excellence.
Oversee patient recruitment, screening, enrollment, and ongoing monitoring to ensure participant safety and protocol compliance.
Review and verify all study documentation including consent forms, case report forms (CRFs), source documents, and regulatory submissions for accuracy and completeness.
Manage data collection, entry, validation, and analysis using statistical software and adhere to CDISC standards for data management.
Coordinate with clinical laboratories for blood sampling, phlebotomy procedures, vital signs measurement, and laboratory result review.
Ensure strict compliance with HIPAA regulations to protect patient confidentiality and privacy throughout all study activities.
Utilize EMR (Electronic Medical Record) systems for accurate documentation of clinical data and patient information.
Conduct regular site visits and audits to monitor trial progress, resolve issues promptly, and maintain high-quality standards.
Prepare detailed reports for sponsors, regulatory agencies, and institutional review boards (IRBs).
Stay current on evolving regulations related to clinical development and incorporate best practices into trial management.

Qualifications

Proven supervising experience in clinical research settings with a track record of managing multiple trials simultaneously.
Extensive knowledge of clinical trials management processes including patient monitoring, data collection, documentation review, and compliance management.
Strong understanding of medical terminology, FDA regulations, ICH GCP guidelines, HIPAA privacy rules, and CDISC standards.
Clinical laboratory experience including blood sampling techniques such as phlebotomy is highly desirable.
Proficiency in statistical software applications used for data analysis within clinical research environments.
Certification in ICH GCP (Good Clinical Practice) from a recognized issuer; additional certifications such as a CA (Clinical Assistant) or related credentials are advantageous.
Background in nursing or related healthcare fields with experience in clinical development or research preferred.
Excellent analysis skills with attention to detail in data management and documentation review.
Ability to lead teams effectively while maintaining high standards of quality assurance throughout all phases of clinical trials. Join us in advancing groundbreaking medical research by applying your expertise as a Senior Clinical Research Coordinator! Your dedication will help shape the future of healthcare while working in a dynamic environment that values innovation and excellence.

Pay: $60,000.00 - $70,000.00 per year

Benefits:

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

Work Location: In person

Quick Apply

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research coordinator jobs in daytona beach fl

Senior Clinical Research Coordinator

Oncology Research Coordinator

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