Clinical Research Protocol Analyst
Location: Horsham Pennsylvania
Description: Acurian is at present looking to employ Clinical Research Protocol Analyst right now, this vacancy will be placed in Pennsylvania. For complete informations about this vacancy opportunity kindly see the descriptions. Role
Acurian is seeking an individual with a comprehensive background in clinical research across multiple therapeutic areas. The Clinical Research Protocol Analyst is a pivotal position in Acurian’s Operations department offering their insight and expertise on the protocol for all of Acurian’s new business opportunities.
The Clinical Research Protocol Analyst is responsible for reading and interpreting the protocol document for each clinical trial that Acurian bids its recruitment services. Upon assessing each new business opportunity, the Clinical Research Protocol Analyst will present their expert analysis of the protocol and their evaluation of the difficulty of enrolling the targeted population. The Protocol Analyst will then collaborate directly with both the statisticians and marketing specialists to develop a recruitment plan for the specific protocol.
Job Functions/Responsibilities Perform feasibility assessment of clinical protocols to assess the challenges of patient recruitment Research standard of care for several therapeutic areas Work collaboratively across multiple teams including Sales, Analytics, Proposals and Media Assist in the development of patient recruitment programs across multiple therapeutic areas Write supportive documentation to serve as basis for proposal assertions Preparation and attendance to bid defense meetings (as required) Requirements Bachelor degree required in Pharmacy, Public Health, Epidemiology, Nursing or similar field Masters degree or Pharm. D. a plus Experience working directly with patients and/or investigators in a clinical research setting (Clinical Research RN, research coordinator, study coordinator or similar) Clinical Research experience in multiple therapeutic areas preferred General knowledge of drug development process and clinical trial regulations Must have an analytical mind with attention to details Persuasive writing skills and the ability to simplify complex medical concepts Strong working knowledge of MS Office Suite (Word, Excel, PowerPoint) Acurian - HR Dept
2 Walnut Grove Drive, Suite 375
Horsham, PA 19044
E-mail: opportunities@acurian.com
Fax: 215-323-9021
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If you were eligible to this vacancy, please email us your resume, with salary requirements and a resume to Acurian.
If you interested on this vacancy just click on the Apply button, you will be redirected to the official website
This vacancy starts available on: Thu, 12 Jul 2012 06:07:00 GMT
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