Job Overview
Employment Type
Full-time
Compensation
Type:
Hourly
Rate:
Range $23.00 - $31.00
Benefits
various annual leave entitlements
health insurance offerings
competitive retirement planning offerings
global employee assistance program with 24-hour access
Life Assurance
subsidised travel passes, health assessments
Job Description
ICON plc is a globally recognized healthcare intelligence and clinical research organization committed to advancing clinical development through innovative approaches and excellence in service. As a world-leading entity in healthcare and clinical research, ICON prides itself on fostering an inclusive culture that drives innovation and supports the professional growth of its employees. Operating on a worldwide scale, ICON provides a dynamic and supportive environment where diverse talents can thrive, contributing to the vital mission of shaping the future of clinical trials and healthcare outcomes. The organization emphasizes teamwork, integrity, and quality in all aspects of its work, ensuring that the... Show More
Job Requirements
- Bachelor's degree
- 2+ years of experience as a clinical research coordinator or equivalent role
- high attention to detail
- ability to communicate effectively
- interest in clinical research career
- ability to perform clinical procedures such as phlebotomy
- capability to manage multiple studies simultaneously
- willingness to work on-site in Charleston, SC
Job Qualifications
- Bachelor's degree
- 2+ years of experience as a clinical research coordinator or equivalent role
- high attention to detail
- strong communication and organizational skills
- proficiency with clinical trial management and electronic data capture systems
- ability to work independently and collaboratively in a team environment
- interest in a clinical research career
Job Duties
- Performs study start-up duties including production of recruitment tools and progress notes, phone screens participants to identify trial candidates on site
- proactively develops and executes recruitment plans to exceed enrollment goals
- completes training and maintains skills in Clinical Trial Management System for database updates, participant reimbursement, referral source capture, and call list creation
- attends investigator meetings
- creates and updates source documents and progress notes using Core Operating Guidelines templates
- accurately collects study data via source documents and progress notes
- performs technical protocol requirements such as phlebotomy, blood pressure measurement, electrocardiograms, pulmonary function testing, allergy testing, pregnancy tests, strep throat screening
- performs continuous inclusion/exclusion criteria reviews and peer reviews for trials
- documents laboratory data and adverse reactions, promptly informs investigators, Institutional Review Board, and sponsors of serious adverse events
- builds and maintains strong relationships with investigators, providing trial status updates
- dispenses study medication as directed by investigators
- maintains communication with sponsor monitors through calls, written communication, and site visits
- enters visit data in Electronic Data Capture or Case Report Forms within sponsor timelines
Job Location
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