Clinical Research Coordinator
Behavioral Health Market Context
Apply Nowvia SimplyHired
Benefits
Health InsuranceDental CoveragePaid Time Off
Job Description
re. This position offers an exciting opportunity to contribute to groundbreaking medical research that impacts patient outcomes worldwide. The ideal candidate will possess strong organizational skills, clinical trial management experience, and a passion for advancing healthcare through research excellence.
Duties
• Coordinate all aspects of clinical trials, including participant recruitment, screening, and enrollment
• Monitor patient progress throughout the study, ensuring adherence to protocols and safety guidelines
• Review and verify study documentation for accuracy, completeness, and regulatory compliance
• Manage data collection and entry using electronic medical record (EMR) systems and adhere to CDISC standards for data management
• Conduct patient assessments such as vital signs, blood sampling (phlebotomy), and clinical laboratory procedures
• Ensure compliance with FDA regulations, ICH GCP guidelines, HIPAA privacy rules, and other applicable standards
• Supervise research staff and collaborate with multidisciplinary teams to maintain high-quality study conduct
• Prepare reports, maintain detailed study records, and assist in audits or inspections as required
Qualifications
• Proven supervising experience in clinical research or healthcare settings
• Strong knowledge of clinical trials management, medical terminology, and regulatory requirements including FDA regulations and ICH GCP certification
• Experience with clinical laboratory procedures such as blood sampling and analysis skills
• Familiarity with EMR systems, data management tools, and statistical software used in research settings
• Understanding of HIPAA compliance, research documentation review, and adherence to CDISC standards for data exchange
• Background in nursing or related healthcare fields preferred; certification in Good Clinical Practice (GCP) is highly desirable
• Excellent organizational skills with attention to detail; ability to manage multiple tasks simultaneously
• Strong communication skills for effective collaboration with team members, participants, and regulatory bodies
Join us in advancing medical science by supporting innovative clinical trials that improve patient health outcomes. We are committed to fostering a diverse environment where your expertise can thrive. All roles are paid positions that recognize your valuable contributions to healthcare research excellence.
Pay: $25.00 - $45.00 per hour
Benefits:
• 401(k)
• 401(k) matching
• Dental insurance
• Health insurance
• Health savings account
• Life insurance
• Paid time off
• Vision insurance
Work Location: Hybrid remote in Dearborn, MI 48126
Duties
• Coordinate all aspects of clinical trials, including participant recruitment, screening, and enrollment
• Monitor patient progress throughout the study, ensuring adherence to protocols and safety guidelines
• Review and verify study documentation for accuracy, completeness, and regulatory compliance
• Manage data collection and entry using electronic medical record (EMR) systems and adhere to CDISC standards for data management
• Conduct patient assessments such as vital signs, blood sampling (phlebotomy), and clinical laboratory procedures
• Ensure compliance with FDA regulations, ICH GCP guidelines, HIPAA privacy rules, and other applicable standards
• Supervise research staff and collaborate with multidisciplinary teams to maintain high-quality study conduct
• Prepare reports, maintain detailed study records, and assist in audits or inspections as required
Qualifications
• Proven supervising experience in clinical research or healthcare settings
• Strong knowledge of clinical trials management, medical terminology, and regulatory requirements including FDA regulations and ICH GCP certification
• Experience with clinical laboratory procedures such as blood sampling and analysis skills
• Familiarity with EMR systems, data management tools, and statistical software used in research settings
• Understanding of HIPAA compliance, research documentation review, and adherence to CDISC standards for data exchange
• Background in nursing or related healthcare fields preferred; certification in Good Clinical Practice (GCP) is highly desirable
• Excellent organizational skills with attention to detail; ability to manage multiple tasks simultaneously
• Strong communication skills for effective collaboration with team members, participants, and regulatory bodies
Join us in advancing medical science by supporting innovative clinical trials that improve patient health outcomes. We are committed to fostering a diverse environment where your expertise can thrive. All roles are paid positions that recognize your valuable contributions to healthcare research excellence.
Pay: $25.00 - $45.00 per hour
Benefits:
• 401(k)
• 401(k) matching
• Dental insurance
• Health insurance
• Health savings account
• Life insurance
• Paid time off
• Vision insurance
Work Location: Hybrid remote in Dearborn, MI 48126
Qualifications
- •The ideal candidate will possess strong organizational skills, clinical trial management experience, and a passion for advancing healthcare through research excellence
- •Proven supervising experience in clinical research or healthcare settings
- •Strong knowledge of clinical trials management, medical terminology, and regulatory requirements including FDA regulations and ICH GCP certification
- •Experience with clinical laboratory procedures such as blood sampling and analysis skills
- •Familiarity with EMR systems, data management tools, and statistical software used in research settings
- •Understanding of HIPAA compliance, research documentation review, and adherence to CDISC standards for data exchange
- •Excellent organizational skills with attention to detail; ability to manage multiple tasks simultaneously
- •Strong communication skills for effective collaboration with team members, participants, and regulatory bodies
Benefits
- •Pay: $25.00 - $45.00 per hour
- •401(k)
- •401(k) matching
- •Dental insurance
- •Health insurance
- •Health savings account
- •Life insurance
- •Paid time off
- •Vision insurance
Responsibilities
- •We are seeking a dedicated and detail-oriented Clinical Research Coordinator to join our dynamic research team
- •In this vital role, you will oversee the planning, execution, and management of clinical trials to ensure compliance with regulatory standards and study protocols
- •Your proactive approach will facilitate smooth operations, accurate data collection, and high-quality patient care
- •This position offers an exciting opportunity to contribute to groundbreaking medical research that impacts patient outcomes worldwide
- •Coordinate all aspects of clinical trials, including participant recruitment, screening, and enrollment
- •Monitor patient progress throughout the study, ensuring adherence to protocols and safety guidelines
- •Review and verify study documentation for accuracy, completeness, and regulatory compliance
- •Manage data collection and entry using electronic medical record (EMR) systems and adhere to CDISC standards for data management
- •Conduct patient assessments such as vital signs, blood sampling (phlebotomy), and clinical laboratory procedures
- •Ensure compliance with FDA regulations, ICH GCP guidelines, HIPAA privacy rules, and other applicable standards
- •Supervise research staff and collaborate with multidisciplinary teams to maintain high-quality study conduct
- •Prepare reports, maintain detailed study records, and assist in audits or inspections as required
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