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WHAT
IN
Clinical Research Associate
Job
KFORCE Professional Staffing
US
-
San Francisco,
California
Job Code - 949865-NRC
Position - Direct Hire
Job First Active on: Thursday, October 29, 2009
APPLY TO THIS JOB (You will be applying directly to KFORCE Professional Staffing for this position!)
JOB DESCRIPTION: Clinical Research Associate
At Kforce Clinical Research, we don't 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 world's 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 In-House Clinical Research Associate in San Francisco, CA. Essential Responsibilities:
* Assist in the design, planning, and implementation of clinical research projects
* Assist in the development of protocols, case report forms, informed consents, study manuals, and study budgets
* Facilitate the negotiation of site contracts and budgets, manage and calculate site payments
* Perform site visits including site qualification, initiation, monitoring and close-out visits, co-monitoring with regional monitors, and reviewing monitoring reports
* Ensure adherence to the protocol providing for accurate data collection, documenting drug accountability, and compliance with federal regulations
* Establish and maintain good relationships with investigators and study site personnel
* Maintain frequent site contact; prepare and track required documentation and manage study supplies at clinical sites
* Oversee and track project progress at assigned sites (patient status, safety/adverse events, CRF completion, payments, study drug supply, and regulatory documents)
* Review data listings on an ongoing basis
* Assist in planning Investigator Meetings
* Assist in preparing interim study analyses, annual reports, and clinical study reports
REQUIREMENTS - QUALIFICATIONS: Clinical Research Associate
Due to the precise requirements of this position, we will only be contacting candidates that meet all of the listed criteria. Clinical Research Associate Qualifications:
* 2 to 3 years of pharmaceutical industry experience including direct site management
* BA/BS degree in Nursing, Pharmacy, Life Sciences, or health-related discipline
* Thorough knowledge of GCP, ICH, and FDA regulations
* Strong organizational skills, detail oriented, and ability to multi-task and work effectively in a fast-paced environment
* Self-motivated, assertive, and able to function independently or as part of a team
* Strong written and verbal communication to include strong interpersonal skills
* Ability to travel 30-40%
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!
KFORCE Professional Staffing
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