Angels Clinical Research Institute
Overview
This is a full-time, on-site role for a Clinical Research Coordinator located in Miami, FL. The Clinical Research Coordinator will be responsible for managing and coordinating all aspects of clinical trials and research studies. Daily tasks include obtaining informed consent from participants, ensuring adherence to study protocols, scheduling and conducting study visits, collecting and documenting research data, and ensuring regulatory compliance. The role also involves collaboration with other research staff, monitoring participant safety, and providing updates to the study sponsor as required. Responsibilities
Manage and coordinate all aspects of clinical trials and research studies Obtain informed consent from participants and ensure adherence to study protocols Schedule and conduct study visits, collect and document research data Ensure regulatory compliance and monitor participant safety Collaborate with other research staff and provide updates to the study sponsor as required Qualifications
Experience in informed consent and protocol adherence Proven clinical research experience and familiarity with clinical trials Strong research and data collection skills Excellent organizational and time-management skills Strong communication and interpersonal skills Ability to work collaboratively with a research team Certification in clinical research (SoCRA, ACRP) is an advantage Seniority level
Entry level Employment type
Full-time Job function
Research, Analyst, and Information Technology Industries
Research Services
#J-18808-Ljbffr
This is a full-time, on-site role for a Clinical Research Coordinator located in Miami, FL. The Clinical Research Coordinator will be responsible for managing and coordinating all aspects of clinical trials and research studies. Daily tasks include obtaining informed consent from participants, ensuring adherence to study protocols, scheduling and conducting study visits, collecting and documenting research data, and ensuring regulatory compliance. The role also involves collaboration with other research staff, monitoring participant safety, and providing updates to the study sponsor as required. Responsibilities
Manage and coordinate all aspects of clinical trials and research studies Obtain informed consent from participants and ensure adherence to study protocols Schedule and conduct study visits, collect and document research data Ensure regulatory compliance and monitor participant safety Collaborate with other research staff and provide updates to the study sponsor as required Qualifications
Experience in informed consent and protocol adherence Proven clinical research experience and familiarity with clinical trials Strong research and data collection skills Excellent organizational and time-management skills Strong communication and interpersonal skills Ability to work collaboratively with a research team Certification in clinical research (SoCRA, ACRP) is an advantage Seniority level
Entry level Employment type
Full-time Job function
Research, Analyst, and Information Technology Industries
Research Services
#J-18808-Ljbffr