Registered Nurse - Clinical Research Coordinator
40–45 an hour
Behavioral Health Market Context
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Benefits
Dental CoverageHealth Insurance
Job Description
documentation. Your expertise will help facilitate groundbreaking research that improves patient outcomes and contributes to the development of innovative therapies. This paid position offers an exciting opportunity to combine nursing skills with research excellence in a collaborative environment.
Duties
• Coordinate and manage all aspects of clinical trials, including participant recruitment, enrollment, and retention
• Monitor patient health and safety throughout the study, conducting vital signs assessments and blood sampling as needed
• Review and verify study documentation for accuracy, completeness, and compliance with FDA regulations and ICH GCP standards
• Collect, manage, and analyze research data using statistical software and adhere to CDISC standards for data formatting
• Ensure adherence to HIPAA regulations by maintaining patient confidentiality and secure handling of sensitive information
• Conduct clinical laboratory procedures such as blood sampling and phlebotomy with precision and care
• Oversee EMR (Electronic Medical Record) systems to document patient interactions, study progress, and adverse events accurately
• Supervise junior staff or research assistants involved in data collection or patient monitoring activities
• Maintain compliance with all regulatory requirements related to clinical development and research protocols
Requirements
• Bachelor’s degree in Nursing (RN) required.
• 1–3 years of clinical research experience preferred.
• Fluency in Spanish required.
• Certification as a Clinical Research Coordinator (CCRC) or Clinical Research Professional (CCRP) is an asset.
• Phlebotomy certification with demonstrated ability to collect, process, and ship specimens in accordance with IATA guidelines.
• Strong knowledge of GCP, FDA, and IRB regulations.
• Excellent organizational, communication, and problem-solving skills.
Join our team to make a meaningful impact on healthcare innovation! We are committed to supporting your professional growth while fostering a vibrant work environment. This role offers the chance to blend nursing expertise with cutting-edge research initiatives—empowering you to contribute directly to advancements in medicine.
Pay: $40.00 - $45.00 per hour
Expected hours: 40.0 per week
Benefits:
• Dental insurance
• Flexible schedule
• Health insurance
Work Location: In person
Duties
• Coordinate and manage all aspects of clinical trials, including participant recruitment, enrollment, and retention
• Monitor patient health and safety throughout the study, conducting vital signs assessments and blood sampling as needed
• Review and verify study documentation for accuracy, completeness, and compliance with FDA regulations and ICH GCP standards
• Collect, manage, and analyze research data using statistical software and adhere to CDISC standards for data formatting
• Ensure adherence to HIPAA regulations by maintaining patient confidentiality and secure handling of sensitive information
• Conduct clinical laboratory procedures such as blood sampling and phlebotomy with precision and care
• Oversee EMR (Electronic Medical Record) systems to document patient interactions, study progress, and adverse events accurately
• Supervise junior staff or research assistants involved in data collection or patient monitoring activities
• Maintain compliance with all regulatory requirements related to clinical development and research protocols
Requirements
• Bachelor’s degree in Nursing (RN) required.
• 1–3 years of clinical research experience preferred.
• Fluency in Spanish required.
• Certification as a Clinical Research Coordinator (CCRC) or Clinical Research Professional (CCRP) is an asset.
• Phlebotomy certification with demonstrated ability to collect, process, and ship specimens in accordance with IATA guidelines.
• Strong knowledge of GCP, FDA, and IRB regulations.
• Excellent organizational, communication, and problem-solving skills.
Join our team to make a meaningful impact on healthcare innovation! We are committed to supporting your professional growth while fostering a vibrant work environment. This role offers the chance to blend nursing expertise with cutting-edge research initiatives—empowering you to contribute directly to advancements in medicine.
Pay: $40.00 - $45.00 per hour
Expected hours: 40.0 per week
Benefits:
• Dental insurance
• Flexible schedule
• Health insurance
Work Location: In person
Qualifications
- •Bachelor’s degree in Nursing (RN) required
- •Fluency in Spanish required
- •Certification as a Clinical Research Coordinator (CCRC) or Clinical Research Professional (CCRP) is an asset
- •Phlebotomy certification with demonstrated ability to collect, process, and ship specimens in accordance with IATA guidelines
- •Strong knowledge of GCP, FDA, and IRB regulations
- •Excellent organizational, communication, and problem-solving skills
Benefits
- •Pay: $40.00 - $45.00 per hour
- •Expected hours: 40.0 per week
- •Dental insurance
- •Flexible schedule
- •Health insurance
Responsibilities
- •We are seeking a dedicated and energetic Registered Nurse to serve as a Clinical Research Coordinator, playing a vital role in advancing medical knowledge through clinical trials
- •In this dynamic position, you will oversee the coordination and management of clinical research studies, ensuring compliance with regulatory standards, safeguarding patient safety, and maintaining meticulous documentation
- •Your expertise will help facilitate groundbreaking research that improves patient outcomes and contributes to the development of innovative therapies
- •This paid position offers an exciting opportunity to combine nursing skills with research excellence in a collaborative environment
- •Coordinate and manage all aspects of clinical trials, including participant recruitment, enrollment, and retention
- •Monitor patient health and safety throughout the study, conducting vital signs assessments and blood sampling as needed
- •Review and verify study documentation for accuracy, completeness, and compliance with FDA regulations and ICH GCP standards
- •Collect, manage, and analyze research data using statistical software and adhere to CDISC standards for data formatting
- •Ensure adherence to HIPAA regulations by maintaining patient confidentiality and secure handling of sensitive information
- •Conduct clinical laboratory procedures such as blood sampling and phlebotomy with precision and care
- •Oversee EMR (Electronic Medical Record) systems to document patient interactions, study progress, and adverse events accurately
- •Supervise junior staff or research assistants involved in data collection or patient monitoring activities
- •Maintain compliance with all regulatory requirements related to clinical development and research protocols
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