Clinical Research Coordinator

About the role

We're looking for someone to join our team who can evaluate, initiate, and maintain all activities related to the conduct of clinical trials. You'll communicate with external funding agencies and sponsors, other departments, and patients to ensure everyone understands the requirements of conducting and participating in clinical trials. You'll also organize and manage all patient care requirements and coordinate complex clinical trials.

Responsibilities

• Organizes strategies for recruiting study participants and screening them for eligibility.
• Coordinates and oversees patient activity related to the conduct of research and clinical trials, acting as a liaison between patient and Principal Investigator (PI).
• Serves as the primary point of contact for patients to report and triage adverse events and independently conducts informed consent.
• Arranges necessary tests and procedures in accordance with protocol requirements and reports results to the investigator.
• Maintains close communication with study sponsor representatives, including site initiation, maintenance, and close out of studies.
• Develops and maintains all required documentation as it relates to the conduct of assigned clinical trials and associated patient care.
• Completes data entry into sponsor-specific data entry systems and/or supports data coordinators, including query resolution and transcribing information across various internal and external electronic data systems.
• Conducts daily work and clinical trial activity in accordance with Good Clinical Practice Guidelines.
• Adapts behavior to the specific patient population, including respecting privacy, adapting explanations, requesting permissions, and communicating effectively.
• Performs other related duties as assigned.

Requirements

• High school diploma or equivalent.
• 3 years of relevant research experience in a clinical setting, or 2 years of relevant research experience with ACRP or SOCRA certification.
• Current Basic Life Support (BLS) certification from the American Heart Association within 60 days of hire.

Qualifications

• Strong critical thinking skills.
• Ability to follow and provide critical feedback on the investigational plan.
• Proficiency in using computers, software, and web-based applications, including working knowledge of Epic.
• Effective verbal and written communication skills and ability to present information clearly and professionally to varying levels of individuals throughout the patient care process.
• Strong organizational and time management skills and ability to multi-task, pay close attention to detail, and learn new techniques.

Skills

• Working knowledge of ICH guidelines for ethical conduct of research.
• Working knowledge of the requirements and regulations associated with the conduct of clinical trials and other related research activity.
• Knowledge of medical and clinical research terminology and processes.
• Proficiency in using computers, software, and web-based applications, including working knowledge of Epic.

Benefits

We offer a comprehensive benefits package designed to support you and your family. This includes health insurance, retirement plans, paid time off, and more. Join us and discover your future today!

Pay

Details on pay will be provided during the interview process.

Schedule

The schedule for this role will be discussed during the interview process.