Description
Clinical Science ConsultantDuties:
* Interact with investigators and thought leaders in oncology to facilitate the design of clinical synopses and protocols.
* In collaboration with the clinical teams for a specific product candidate, design, prepare and initiate study protocols and other required documentation in compliance with project plans, federal regulations, GCP and good medical practice. Research and assist in the selection of investigators.
* Support the clinical leader for one or more compounds in clinical development
* Support product specific publication plans, develop and manage timelines of such publication plans.
* Analyze and interpret study data and support preparation of reports for the FDA and publication. Proactively provide feedback on emerging clinical and competitive trends.
* Demonstrate thorough understanding of both clinical and commercial strategies and priorities.
* Coordinate and facilitate oncology trials by developing and maintaining excellent working relationships with study investigators.
Education:
* BS/BA degree in related discipline and eleven years of related experience; or,
* MS/MA degree in related discipline and nine years of related experience; or,
* Pharm.D., PhD or M.D. in related discipline and five or more years of related experience, or;
* Equivalent combination of education and experience.
* May require certification in assigned area.
Experience:
* Typically requires a minimum of 15 years of related experience and/or combination of experience and education/training.
* Experience in Biotech/Pharmaceutical industry preferred.
* Experience in Clinical (Oncology) industry required.
To find out more about Real please visit www.realstaffing.com