Registered Nurse Coordinator I

Duties & Responsibilities

• Assist with patient screening and recruitment for clinical trials.
• Support the informed consent process under the direct supervision of a senior CRC or manager.
• Perform basic clinical data entry and management into Electronic Data Capture (EDC) systems.
• Absorb scheduling patient visits and procedures.
• Help with the preparation of source documents and study binders.
• Maintain inventory of study supplies and equipment.
• Handle processing and shipment of lab samples following IATA/DOT regulations (with training).
• Attend study meetings and complete required training (GCP, HIPAA, Protocol-specific).
• Perform nursing assessments and conduct protocol-related procedures (vitals, ECGs, infusions, pharmacokinetic sampling, etc.).
• Administer investigational products (drugs, devices, biologics) per protocol.
• Monitor patient responses to investigational products and provide clinical care.
• Assess, document, and report Adverse Events (AEs) and Serious Adverse Events (SAEs) to the PI and sponsor.
• Provide patient education and serve as a clinical resource for participants throughout the study.

Qualifications & Skills

• Current Registered Nurse (RN) license in the applicable state
• 1 year of Nurse experience
• Basic understanding of medical terminology
• Strong attention to detail and organizational skills
• Ability to follow detailed instructions and protocols
• Good written and verbal communication skills
• Proficient with basic computer software (MS Office)
• Comfortable working in hospital and clinical care environments, including direct patient interaction and collaboration with physicians and other healthcare professionals
• Must be willing and able to travel between hospitals, clinics, and other office locations as needed to support research activities