Job Overview
Employment Type
Full-time
Compensation
Type:
Hourly
Rate:
Range $22.00 - $30.00
Work Schedule
Standard Hours
Benefits
annual leave
Health Insurance
Retirement Planning
Employee assistance program
Life Assurance
Flexible benefits
Paid Time Off
Job Description
ICON plc is a globally recognized healthcare intelligence and clinical research organization dedicated to advancing the future of clinical development. With a steadfast commitment to innovation and excellence, ICON fosters an inclusive culture that supports diversity and drives progress in the clinical research field. As a leader in healthcare, the company offers a dynamic environment where professionals can contribute meaningfully to life-changing research efforts that improve patient outcomes worldwide. ICON operates through a network of specialized clinical sites and strategic partnerships that streamline clinical trial processes and enhance accessibility for patients and sponsors alike.
The Clinical Research Coordinator ... Show More
The Clinical Research Coordinator ... Show More
Job Requirements
- Bachelor's degree in life sciences or related field
- minimum 1 year of clinical research or pharmaceutical work experience
- prior experience as a Clinical Research Coordinator
- experience with neurology or psychiatric clinical trials
- strong attention to detail
- motivated and committed to a career in clinical research
- excellent time management and organizational skills
- ability to perform clinical procedures as required by study protocols
Job Qualifications
- Bachelor's degree in life sciences or related field
- 1+ years work experience in clinical research or pharmaceutical environment
- prior CRC experience
- experience with neurology or psychiatric clinical trials
- strong attention to detail
- motivated about career in clinical research
- excellent time management and planning skills
- organized approach to work
Job Duties
- Performing technical and clinical requirements of study protocols, attending investigator and coordinator meetings to obtain training, obtaining knowledge about study drugs, monitoring complications with drug administration, maintaining accurate dispensing logs, documenting laboratory data and adverse reactions, assisting other staff members, actively recruiting suitable participants for clinical trials, promoting the site with monitors and in-house contacts, responding to queries promptly, preparing study documentation for audits, ordering clinical supplies and monitoring rescue drugs, monitoring refrigerators and investigational product storage temperatures, maintaining knowledge of temperature monitoring devices, maintaining certification for packaging and shipping specimens, acting as OSHA representative including immunization record management, performing equipment calibration and maintaining records, supporting training and development of clinical skills for staff
Job Qualifications
Experience
Mid Level (3-7 years)
Job Location
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