Job Overview
Employment Type
Full-time
Compensation
Type:
Hourly
Rate:
Range $22.00 - $30.00
Work Schedule
Standard Hours
Benefits
various annual leave entitlements
Health Insurance
Retirement Planning
Employee assistance program
Life Assurance
Flexible country-specific optional benefits
Job Description
ICON plc is a world-leading healthcare intelligence and clinical research organization dedicated to advancing medical knowledge and improving patient outcomes through innovative clinical research solutions. With a global presence, ICON specializes in providing comprehensive services that span clinical development, data analytics, and strategic consulting. The company fosters an inclusive work environment that values innovation, excellence, and collaboration among its employees. ICON's commitment to driving advancements in healthcare has positioned it as a trusted partner for pharmaceutical, biotechnology, and medical device companies worldwide.
This role is specifically within Accellacare, a key component of ICON's clinical research network. Accellacare is focused on... Show More
This role is specifically within Accellacare, a key component of ICON's clinical research network. Accellacare is focused on... Show More
Job Requirements
- bachelor's degree in life sciences or equivalent industry experience
- minimum one year of experience in clinical research or pharmaceutical setting preferred
- strong attention to detail
- effective communication and interpersonal skills
- motivated and organized work approach
- ability to handle multiple tasks and adhere to protocols
- willingness to participate in ongoing training and development
Job Qualifications
- bachelor's degree in life sciences or relevant field
- relevant experience in clinical research or pharmaceutical environment desirable
- high level of attention to detail
- excellent organizational and planning skills
- personable with ability to build rapport with patients
- motivated for a career in clinical research
Job Duties
- performing technical and clinical requirements of study protocols including venipuncture and specimen processing
- attending investigator meetings and site initiation visits for protocol training
- obtaining knowledge about study drugs with emphasis on injection or intravenous infusion medications
- monitoring for possible complications associated with study drug administration
- maintaining accurate dispensing logs including drug lot numbers and placebo information
- documenting laboratory data and adverse reactions and notifying investigators and sponsors as needed
- assisting staff based on organizational needs and priorities
- actively recruiting and promoting clinical trial services to potential participants
- proactively engaging with monitors and contacts for future trial opportunities
- responding promptly to queries and ensuring timely data entry during on-site visits
- preparing study documentation for sponsor or FDA audits and supporting auditors
- ordering clinical supplies and managing emergency equipment including code carts and AEDs
- monitoring and maintaining storage temperatures for specimens and investigational products
- maintaining knowledge and certification for packaging and shipping specimens
- acting as the site OSHA representative including maintaining immunization records and administering vaccines
- performing equipment calibration and maintaining calibration records
- supporting training and skill development of site staff
Job Qualifications
Experience
Entry Level (1-2 years)