Charge Nurse, Nights - Pharmaceutical Research
Location: Overland Park Kansas
Description: Quintiles Transnational is at present recruited Charge Nurse, Nights - Pharmaceutical Research right now, this position will be placed in Kansas. For detail informations about this position opportunity kindly read the description below. Quintiles pioneered the idea of helping pharma companies conduct objective clinical trials to establish not only whether a drug is eff! ective, but who can take it safely. Our customers have relied on us to design and conduct rigorous clinical research for decades, from small studies to multinational mega-trials. However, we continue to develop new ways of interpreting and evaluating data that allow us to create more effective trials and determine outcomes faster. If that is your passion, we have a place for you.
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 Charge Nurse working the night shift, three 12-hour shifts per week. Variable schedule to include holidays.
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 app! licable guidelines and regulations. In addition, you will assist with the guidance and supervision of staff in this role. 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.
Manage the unit after hours in the absence of senior staff, escalating problems to senior staff as required.
Quintiles offers a great work environment and a generous benefit package. Apply now if you are interested in contributing to the advancement of medicine!
A sign on bonus will be part of the compensation package.
Bachelor's degree or educational equivalent in Nursing and 3 years relevant experience; or equivalent combination of education, training and experience
Must possess a current RN license in the State of Kansas
Good knowledge of Phase I clinical trials
In-depth knowledge of department! al, protocol and study-specific operating procedures, consent forms, an! d study schedules
Knowledge of Microsoft Office Products
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If you were eligible to this position, please email us your resume, with salary requirements and a resume to Quintiles Transnational.
If you interested on this position just click on the Apply button, you will be redirected to the official website
This position starts available on: Thu, 11 Apr 2013 11:54:04 GMT
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