Senior Clinical Research Associate- Oncology

renderImage('http://www.cybercoders.com/images/search.png', 84, 39); Specifications Location   Princeton, NJ; Kingston, NJ Salary   $70,000 - $100,000 Education   Bachelor of Science Category   Research Experience Required   At least 2 Years Short Description   Senior Clinical Research Associate - Oncology Required Skills   Senior Clinical Research Associate - Oncology, Directing monitoring experience, Clinical development process CGPs/ICH guidelines, Oncology, Transplantation, Immunology, MW WOrd, MS Project, Excel Recruiter   Avis Evans Date Updated   5/10/2008 Job Description Skills Required Senior Clinical Research Associate - Oncology, Directing monitoring experience, Clinical development process CGPs/ICH guidelines, Oncology, Transplantation, Immunology, MW WOrd, MS Project, Excel Job Description Our Client, a large pharmaceutical company in northern, NJ is looking for a Sr. CRA to join their dynamic team. This is an In-House opportunity on an Oncology study that will require up to 40% travel.Position Overview:As member of therapeutically aligned Clinical Study Management team, the Clinical Research Associate will be responsible for supporting the Clinical Project Manager with the planning, implementation, monitoring and management of clinical studies. What you will be doing:- Working with Clinical Project Manager to organize and facilitate the overall activities required to plan, coordinate, track and manage the general performance of clinical trials. - In-house and field site monitoring of clinical trial investigational sites to ensure study protocol compliance in adherence to GCP/ICH guidelines. - Communicating with sites to ensure study procedures are followed, to collect essential trial information, to address and resolve study-related issues. - Maintaining accurate study data to track enrollment, study supplies and milestone payments. - Conducting pre-study, site initiation, interim monitoring and site close-out visits with resulting visit reports. - Ensuring study data and drug accountability records are accurate and verifiable. - Collecting, maintaining and managing study documents and files within Trial Master File. - Maintaining study-related information within Clinical Trial Management System. - Supporting Clinical Project Manager with developing study-specific documents and operational procedures related to all phases of conducting clinical studies from start-up to close-out. - Assisting Clinical Project Manager with compiling study data for reporting to cross-functional teams and senior management. What you need:- Bachelor degree required preferably in the life sciences - A minimum of five years clinical research experience with a minimum of 3-4 year's direct monitoring experience. - Demonstrated knowledge of the clinical development process/GCPs/ICH guidelines. - Knowledge in the following therapeutic areas: Oncology, Transplantation or Immunology. - Computer literacy in, MS Word, MS Project and Excel. - Effective communication (verbal and written) and organizational skills. - Excellent interpersonal skills. - Must be willing to travel up to 40% domestically, as required. Sound like the career for you? If so, apply now! Location: Princeton, New Jersey; Kingston, New Jersey Want to interview today? Click Here to Do a Quick 2-Minute Online Interview! Are you a fit for this position? Please Click Here to Apply! (your information will be kept strictly confidential!) Looking forward to receiving your resume through our website and going over the position with you. Clicking apply is the best way to apply, but you may also: Email your resume in Word to: Avis.Evans@CyberCoders.com **Please do NOT change the email subject line in any way. You must keep the JobID: CC MonsterAp : AE-LCR -- in the email subject line for your application to be considered.*** Avis Evans - Executive Recruiter - CyberScientific   logET();PauseFooter(false);