Clinical Research Coordinator

Overview Join our dynamic team as a Clinical Research Coordinator and play a vital role in advancing medical research and patient care. In this energetic position, you will oversee the planning, execution, and management of clinical trials, ensuring compliance with regulatory standards and maintaining high-quality data collection. Your expertise will help bring innovative treatments from the laboratory to real-world application, making a meaningful impact on patient outcomes. This paid opportunity offers a chance to develop your skills in clinical development while working in a collaborative and supportive environment. Responsibilities 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 clinical documentation for accuracy, completeness, and compliance with FDA regulations and ICH GCP standards Collect, manage, and analyze clinical data using electronic medical record (EMR) systems and statistical software tools Conduct patient assessments such as vital signs, blood sampling (phlebotomy), and other clinical procedures with precision Maintain regulatory compliance by reviewing study documentation, managing protocol deviations, and ensuring adherence to HIPAA privacy standards Supervise research staff and collaborate with multidisciplinary teams to ensure smooth trial operations Requirements Proven supervising experience in clinical research or related healthcare settings Strong knowledge of clinical trials management, FDA regulations, ICH GCP guidelines, and CDISC standards for data collection Familiarity with medical terminology, clinical laboratory procedures, and EMR systems Experience in patient monitoring, blood sampling (phlebotomy), and vital signs assessment Ability to review complex documentation accurately while maintaining meticulous records Proficiency with statistical software for data analysis and interpretation Certification in Good Clinical Practice (GCP) from a recognized issuer (such as CA or equivalent) is required; an ICH GCP certificate is highly preferred Background in nursing or clinical laboratory work is advantageous Strong analysis skills combined with excellent organizational abilities to ensure compliance management and research integrity Embark on a rewarding career that combines scientific rigor with compassionate patient care. We're dedicated to supporting your professional growth while making a difference in healthcare innovation!

Pay:

$26.00

• $42.

00 per hour

Experience:

Clinical trials: 2 years (Required)

Work Location:

Hybrid remote in Fresh Meadows, NY 11366 Clinical Research Coordinator 16040 78th Rd, Fresh Meadows, NY 11366 Hybrid work $26

• $42 an hour
• Temporary, Part-time, Full-time, Contract $26
• $42 an hour
• Temporary, Part-time, Full-time, Contract Overview Join our dynamic team as a Clinical Research Coordinator and play a vital role in advancing medical research and patient care.

In this energetic position, you will oversee the planning, execution, and management of clinical trials, ensuring compliance with regulatory standards and maintaining high-quality data collection. Your expertise will help bring innovative treatments from the laboratory to real-world application, making a meaningful impact on patient outcomes. This paid opportunity offers a chance to develop your skills in clinical development while working in a collaborative and supportive environment. Responsibilities 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 clinical documentation for accuracy, completeness, and compliance with FDA regulations and ICH GCP standards Collect, manage, and analyze clinical data using electronic medical record (EMR) systems and statistical software tools Conduct patient assessments such as vital signs, blood sampling (phlebotomy), and other clinical procedures with precision Maintain regulatory compliance by reviewing study documentation, managing protocol deviations, and ensuring adherence to HIPAA privacy standards Supervise research staff and collaborate with multidisciplinary teams to ensure smooth trial operations Requirements Proven supervising experience in clinical research or related healthcare settings Strong knowledge of clinical trials management, FDA regulations, ICH GCP guidelines, and CDISC standards for data collection Familiarity with medical terminology, clinical laboratory procedures, and EMR systems Experience in patient monitoring, blood sampling (phlebotomy), and vital signs assessment Ability to review complex documentation accurately while maintaining meticulous records Proficiency with statistical software for data analysis and interpretation Certification in Good Clinical Practice (GCP) from a recognized issuer (such as CA or equivalent) is required; an ICH GCP certificate is highly preferred Background in nursing or clinical laboratory work is advantageous Strong analysis skills combined with excellent organizational abilities to ensure compliance management and research integrity Embark on a rewarding career that combines scientific rigor with compassionate patient care. We're dedicated to supporting your professional growth while making a difference in healthcare innovation!

Pay:

$26.00

• $42.

00 per hour

Experience:

Clinical trials: 2 years (Required)

Work Location:

Hybrid remote in Fresh Meadows, NY 11366