Google Groups no longer supports new Usenet posts or subscriptions. Historical content remains viewable.
Dismiss

US-MD: Ellicott City-Clinical Research Coordinator (RN) - Ellicott City, MD

0 views
Skip to first unread message

JobCircle.Com

unread,
Jul 7, 2008, 5:42:45 AM7/7/08
to
**************************************************************
JobCircle.com is a regional job board serving all industries
and occupations in the PA, NJ, DE, NY, MD, and DC areas.

We offer a regional job board, online learning, and regional
job fair events for jobseekers who live in our areas of focus.

To Learn More:

Job Board: http://www.JobCircle.com?source=ng
eLearning: http://www.JobCircle.com/courseware?source=ng
Job Fairs: http://JobCircleJobFairs.com?source=ng

**************************************************************

Job Title: Clinical Research Coordinator (RN) - Ellicott City, MD
Job Location: MD: Ellicott City
Pay Rate: Open
Job Length: full time
Start Date: 2008-07-06

Company Name: Soliant Health
Contact: Human Resources
Phone: email only please
Fax: email only please

Description: Clinical Research Coordinator (RN) - Ellicott City, MD

Job Search Options

> Apply to this Job! > Tell a Friend! > Back to Search Results > Start a New Search

Current Search Criteria Keywords: Locations: ANY Category: ANY Job Code: 460621 Job Location: Ellicott City, MD Category: Clinical Research Coordinator (CRC) Last Updated: 05/01/2008 Client seeks highly motivated and organized individuals to support pharmaceutical and medical device in-patient cardiac surgery clinical trials at busy open-heart unit at INOVA Fairfax Hospital. Requirements: CCRC preferred but not required ? RN required. Non-RNs will not be considered for this position regardless of research experience. ? At least two years of recent clinical experience strongly preferred ? Ability to work well with co-workers, peers, monitors and potential subjects ? Strong background in cardiac surgery preferred ? Phlebotomy skills preferred ? Shift flexibility is a must Job Responsibilities include: ? Maintain a high level of knowledge and understanding of assigned protocols, including all protocol requirements for patient visits, obtaining informed consent, patient visit schedules, test procedures, laboratory information, and drug accountability requirements. ? Responsible for completion of all study documentation forms, including case report forms and other study specific documents. ? Coordinate and conduct patient care visits and assure all procedures are conducted in compliance with the clinical protocol. ? Interact with Principal Investigator as needed to assure patient receives appropriate medical evaluation and care when needed, alerts Principal Investigator of serious adverse events. ? Interacts with sponsor Clinical Research Associate to facilitate the sponsor monitoring and database clean-up process. ? Attends sponsor Investigator/Study Coordinator meetings as needed for assigned protocols ? Conducts clinical research in compliance with all applicable regulations. Please forward all resumes to jason....@soliant.com


Please refer to Job code soliant-460621 when responding to this ad.


For FASTEST PROCESSING of your resume, please visit http://www.jobcircle.com/classifieds/1510068.html?source=ng to apply online.


**************************************************************
For fastest processing of your resume, this employer asks that
you apply to this job using the URL above.
**************************************************************

0 new messages