Study Coordinator

Rho, Inc. is a premier contract research organization that specializes in enhancing the quality and speed of clinical trials, helping pharmaceutical and biotechnology companies swiftly market new products.  We provide our customers with high quality and timely services in the design, development, and execution of clinical research projects, the collection, processing, and management of clinical trials data, and the statistical analysis and reporting of trial results.  With over 20 years of excellence, Rho has proven itself an effective partner in providing clinical research services that generate significant value to our clients' development programs.


 

The Study Coordinator will be responsible for the overall coordination of study activities, including data collection, data management, SAE reporting, clinical monitoring, and statistical analysis and reporting. Will also coordinate protocol development, study initiation, and study conduct at clinical sites around the country.  The Study Coordinator will maintain contact with the clinical sites; coordinate and track all aspects of the study; and ensure the highest quality deliverables while meeting aggressive deadlines.

 

Must have excellent oral and written communication, problem solving and organizational skills and a demonstrated ability to manage multi-faceted project tasks.  Must also have skills to ensure that projects are conducted in full compliance with standards for safety and quality.  Requires a Bachelor's degree and a minimum of 3 years experience in the pharmaceutical industry or in the conduct of clinical trials.  Advanced degree in nursing or public health is preferred.

 

Please apply by submitting your resume and cover letter with salary requirements to our website at www.rhoworld.com/hr

 

Rho, Inc. is an Equal Opportunity Employer.