Description
ICON is seeking a Clinical Research Coordinator Nurse (CRC Nurse) to join its Accellacare team. The successful candidate will be responsible for completing trial assignments in an autonomous, accurate, and timely manner. The CRC Nurse will perform technical and clinical requirements of study protocols as ordered by the investigator.
Responsibilities:
- Coordinating and conducting clinical trial procedures according to protocol requirements
- Performing technical and clinical requirements of study protocols, such as venipuncture, specimen processing, vital signs, electrocardiograms, IV infusions, IV pump operations, Holtor monitoring, pulmonary function testing, allergy testing, urine/serum pregnancy testing, strep throat screening, injections (IM or SQ) or any procedure necessary for the protocol as ordered by the investigator
- Collecting and documenting patient data accurately and efficiently
- Assisting in patient recruitment, screening, and enrollment processes
- Providing nursing care and support to trial participants
- Collaborating with interdisciplinary teams to ensure trial compliance and quality data collection
Requirements:
- Bachelor's degree in Nursing or equivalent qualification
- LPN required, RN preferred
- Prior experience in clinical research coordination (preferred)
- Strong understanding of GCP guidelines and regulatory requirements
- Excellent communication skills
- Organizational skills with attention to detail
- Problem-solving skills
Rewards & Benefits:
- Competitive base salary and performance-related incentives
- Health and wellbeing programmes including medical, dental, and vision coverage where applicable
- Retirement and pension plans
- Life assurance and disability coverage
- Employee assistance programmes and wellbeing resources
- Learning and development opportunities through structured training and career pathways