Description
ICON is seeking a Clinical Research Coordinator 2 to join its Accellacare team in Knoxville, TN. The successful candidate will ensure the safety of volunteers, promote the mission of Accellacare, and strive to meet and exceed study priorities.
Responsibilities:
- Perform study start-up duties, including production of recruitment tools and progress notes, and phone screening patients
- Develop and execute recruitment plans to meet and exceed enrollment goals
- Complete training on Clinical Trial Management System and maintain proper skills to update database and complete participant reimbursement
- Attend investigator meetings and create and update source documents/progress notes
- Accurately collect study data via source documents/progress notes as required by the protocol
- Perform technical requirements of the study protocol, such as lab work and blood pressure monitoring
- Build and maintain strong relationships with Investigators and provide ongoing communication about trial status and participants
- Dispense study medication at the direction of the Investigator and maintain communication with the monitor from the sponsoring company
Requirements:
- 2+ years of experience as a Clinical Research Coordinator
- Strong attention to detail and excellent time management and planning skills
- Bachelor's degree in life sciences or other related field
Rewards & Benefits:
- Competitive base salary and performance-related incentives
- Health and wellbeing programmes, including medical, dental, and vision coverage
- 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