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Title : OCA- Clinical Research Associate III -971
State : New Jersey   Date : Jan 9, 2019
Experience Level :  
Position Type : Clinical Research Associate III      
Description
This position is for a leading pharmaceutical company. Below are the details of the engagement. If you are available and interested please send me your updated word resume & your expected hourly rate on W2 ASAP.
Looking forward to hearing from you soon.

Work Location: Raritan, NJ


Job Title: Clinical Research Associate III 


Duration:  6+ months (extendable) contract on W2


Duties:


Under supervision of Clinical Project Lead, assists in the implementation, execution and evaluation of systematic literature review activities. Responsibilities include: Conducts systematic literature reviews on cardiovascular biomarkers. Conducts the study eligibility assessments e.g. conducts screening of abstracts and full-text articles against defined inclusion/exclusion criteria to assess their suitability for inclusion in the review. Conducts data extraction and performs critical appraisal of selected studies. Collects back-up source documentation, as required. Develops, updates and maintains study databases and source document worksheets. Assists in development and preparation of systematic review reports. g.g. synthesizing the evidence by through drafting and editing sections of project deliverables. Performs other related duties as assigned



Skills:


Strong knowledge in systematic review methods and clinical research design the field of cardiology, is preferred. Demonstrated ability and knowledge in use PubMed/ Medline, Google Scholar, Microsoft Office Software, and Reference Manager (e.g., EndNote). Proven oral and written communication skills. Knowledge of applicable standards and regulations for clinical trials. Ability to work independently and within a cross-functional team environment to identify and escalate activities issues to the management team in a timely fashion. Proven planning skills; ability to create and track detailed project plans. Proven interpersonal, leadership, organizational and effective time management skills | Preferred: Experience in Cardiovascular Therapeutic area. Experience in systematic literature review methods for diagnostics. IVD Clinical Trial | Travel: 0-10% on an annual basis



Education:


Advanced Degree MD, PhD, MS is desirable 


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Many Thanks,   

Sree Kanth
Associate Recruitment Manager
Sree@newageclinical.com

NewAgeSys, Inc.
Direct: 609-945-1736 Fax: 609-228-4079
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Princeton , NJ 08540 
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