Job Overview
Employment Type
Full-time
Compensation
Type:
Hourly
Rate:
Range $22.25 - $29.75
Work Schedule
Standard Hours
Benefits
Health Insurance
Dental Insurance
Paid Time Off
Competitive retirement plans
Life Assurance
Flexible benefits
Employee assistance program
Job Description
ICON plc is a globally renowned healthcare intelligence and clinical research organization dedicated to advancing innovation and excellence in clinical development. With a commitment to fostering an inclusive environment, ICON drives forward the future of clinical trials by combining cutting-edge science with compassionate care. As a leading provider in the healthcare sector, ICON operates across various domains including pharmaceuticals, biotechnology, and medical devices, helping to bring new and effective therapies to patients worldwide. The company is known for its collaborative culture, comprehensive training programs, and strong emphasis on employee growth and development. ICON welcomes applicants from diverse backgrounds and prioritizes... Show More
Job Requirements
- Bachelor's degree in life sciences or related field
- Minimum one year experience in clinical research or pharmaceutical environment
- Prior experience as Clinical Research Coordinator
- Knowledge of clinical procedures and study protocol requirements
- Ability to perform technical tasks such as venipuncture and IV infusions
- Strong organizational and documentation skills
- Effective communication skills
- Commitment to patient safety and protocol compliance
Job Qualifications
- Bachelor's degree in life sciences or related field
- At least one year of work experience in clinical research or pharmaceutical environment
- Prior experience as a Clinical Research Coordinator
- Familiarity with neurology or psychiatric clinical trials
- Strong attention to detail
- Excellent time management and planning skills
- Motivated for a career in clinical research
Job Duties
- Perform technical and clinical requirements of study protocols including 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)
- Attend investigator meetings, site initiation visits, and coordinator meetings for training on drug preparation, administration, and protocol knowledge
- Obtain knowledge about study drugs especially injection or intravenous infusion medications
- Monitor for complications with administration of study drugs focusing on injections or IV infusions
- Maintain accurate dispensing logs including lot numbers, drug vs placebo, and information about medication preparers
- Document laboratory data and adverse reactions, promptly notifying investigators, sponsors, and Institutional Review Board of unexpected or serious events
- Assist other staff based on research priorities and available time
- Actively recruit and promote services to suitable patient participants for clinical trials
- Promote the site with monitors and in-house contacts for future trials
- Respond to queries timely, enter data promptly, and work with monitors during on-site visits
- Prepare study documentation for sponsor or FDA audits and assist auditors
- Order clinical supplies and monitor protocol-specific rescue drugs and emergency equipment
- Maintain refrigerators, freezer units, and investigational product storage temperature safety
- Maintain certification for specimen packaging and shipping
- Serve as OSHA Representative including managing employee immunization records and administering vaccines
- Perform equipment calibration and maintain calibration records
- Support training and clinical skills development for site staff
Job Qualifications
Experience
Mid Level (3-7 years)
Job Location
OysterLink supports hiring across hospitality industries.
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