Quintiles is the only fully integrated BioPharmaceutical services company offering clinical, commercial, consulting and capital solutions worldwide. The Quintiles network of 23,000 engaged professionals in more than 50 countries around the globe works with an unwavering commitment to patients, safety and ethics. Quintiles helps biopharmaceutical companies navigate risk and seize opportunities in an environment where change is constant. For more information, please visit www.quintiles.com. Various compensation and benefits programs are available depending on position, years of experience and geographic location. Many of the benefits of working with Quintiles go beyond financial re-numeration and include job related training, company recreational events, and community support activities.

Quintiles is an Equal Opportunity Employer M/F/D/V.

In Quintiles' Phase I Clinic, research studies are conducted each year that identify the medicines that will help people live happier and healthier lives. The medical professional who provides care and support for study volunteers are at the forefront of drug development. It's work worth doing. We currently have an exciting career opportunity for a Clinical Research Nurse PRN with shift availability of evenings, nights, and weekends.
 
In this position, you will coordinate and participate in Phase I clinical research studies ensuring that studies are carried out according to protocol, standard operating procedures, and applicable guidelines and regulations. Additional responsibilities may include: 
 
• Coordinate and participate in clinical research studies conducted by a supervising investigator to ensure that data collected on study volunteers adhere to study protocol; may assist in screening volunteers for inclusion in study based on pre-determined criteria.
• Administer investigational drugs to volunteers according to study protocol.
• Confer with volunteers to explain purpose of study and obtain informed consent forms; explain procedures and practical issues such as timelines for visits and restrictions on food and drink.
• Record volunteer clinical data in case report forms (CRFs). Collaborate closely with study investigator informing on relevant adverse events and serious adverse events according to procedures outlined in the protocol.
• Review CRFs; evaluate and interpret collected data and prepare protocol summary forms, statistical reports and analyses documenting progress, adverse trends and appropriate recommendations or conclusions.
• Cooperate with study monitor and reserve sufficient time for questions during monitoring.
• Participate in project meetings with clients and other members of the project team as needed. 
 
This is a PRN position. You must be available to work evenings or nights and some weekends and work full time days for your first week of orientation. Apply now for a great opportunity with a remarkable company!

• Bachelor's Degree or equivalent work experience performing professional nursing in an outpatient clinical setting for a minimum of 1 year


• Must possess a current RN license in the State of Kansas


• Good knowledge of Phase I clinical trials


• In-depth knowledge of the principles of Good Clinical Practices (GCP)


• Willingness to obtain ACLS within 6 months of hire, only if telemetry monitoring


• Knowledge of Microsoft Office Products