Clinical Data Coordinator

At Kforce Clinical Research, we dont just offer jobs. We offer a rewarding career experience, complete with professional development opportunities and a great benefits package! We are intelligent business partners to some of the worlds most valued pharmaceutical companies and have evolved to create models of operational excellence that incorporate Lean and Six Sigma philosophies. Using these tools, Kforce is able to better plan and anticipate work loads and thus minimize the peaks of work that can swamp you. This allows you to stay just as dedicated and still strike a balance between work and home. Currently, one of our top clients is in search of an exceptional Clinical Data Coordinator in Murray Hill, NJ. This data coordinator will serve as the technical leader on all data management aspects for clinical studies, including start-up, maintenance, and completion activities. The primary purpose and objective of this position is to standardize process and implement best practices in an effort to improve quality, streamline data cleaning efforts and deliver analyzable databases within agreed upon project timelines. He / she will perform and / or coordinate the following activities: development of data specifications and the data management plan, participate in the validation of the clinical database, conduct data review, query generation, data coding, electronic data reconciliation, and identify protocol deviations. The data coordinator will manage workflow and oversee data management activities performed by in-house data entry / review project staff and or selected CROs. Requirements: Qualifications: * Undergraduate degree, appropriate certification or equivalent clinical data management experience (Pharmaceutical, CRO or device) is required * 5 years of Data experience with Oracle Clinical * EDC experience is preferred * Fundamental knowledge of adverse event and medication coding dictionaries is preferred * Expert in the use of data management applications * Experience with Excel * Understand clinical research process and regulatory requirements * Able to acquire and apply new technical skills * Establishes rapport and collaborates with others (internal and external) team members; builds constructive and effective relationships * Anticipates problems, issues, and delays; proactively looks to minimize the impact to the project * Follows through on all tasks and ensures quality results Due to the precise requirements of this position, we will only be contacting candidates that meet all of the listed criteria. Kforce Clinical Research has been serving the pharmaceutical industry since 1988. We are truly a career destination and the employer of choice for skilled, dedicated professionals like you. At Kforce, one of our core principles is: Great People = Great Results! This means that we will work to find you the right career match through exceptional customer service, a disciplined process, and personal respect. If you are qualified and interested in the excellent career opportunities we have for you, apply today!

Please refer to job code 1696NRC950545P199 when responding to this ad.

Category:	Biotech/Pharmaceutical
	> Clinical Data Management
Location:	Murray Hill, NJ
County:	County
ZIP Code:
Pay Rate:	Open
Job Terms:	full time
Company:	Kforce Inc.
Phone:	email only please
Fax:	email only please