Clinical Research Coordinator

Benefits

Qualifications

• •Proficient in phlebotomy and associated techniques
• •Experience with lab processing and shipping of biological samples
• •Ability to perform EKGs and pulmonary function tests (PFTs)
• •Skilled in obtaining detailed medical histories from patients
• •Competent in obtaining informed consent from study participants
• •Strong patient care skills with a focus on empathy and communication
• •Medical Assistant, LPN or in a relevant health care field
• •2 years of experience as a Clinical Research Coordinator or in a similar role
• •In-depth knowledge of clinical research processes, regulatory requirements, and GCP
• •Excellent organizational, communication, and interpersonal skills
• •7 more items(s)

Responsibilities

• •The ideal candidate will have a strong background in clinical trials
• •You will play a crucial role in coordinating and overseeing clinical trials, ensuring compliance with regulatory requirements, and facilitating collaboration among study participants, investigators, and sponsors
• •Coordinate and manage clinical trials
• •Ensure adherence to study protocols, Good Clinical Practice (GCP), and regulatory guidelines
• •Recruit, screen, and enroll study participants, obtaining informed consent
• •Report on trial progress, including data collection and management
• •3 more items(s)