SR. CLINICAL SCIENTIST

Top 10 Pharmaceutical Company with a location in Collegeville PA is seeking a consulting Sr. Clinical Research Scientist to join their team.

Requirements:
RN or BSN with 2 years experience in similar position in a pharmaceutical company. Experience with data review, site communication, and serious adverse events is required. 5 years of experience in Protocol writing, site management, regulatory submission and report writing . Team player, good communication skills, does not need extensive supervision or training. Also experience with Drafting protocols, with CRF development, Formulate requirements for clinical supplies, Data review, Site communication, and Handling of Serious Adverse Events

Complete Description:
Drafts protocols, reviews data in CDRS (Clinical Data Review System - an electronic system for reviewing data on line), handles AEs and SAEs, provides scientific input on conduct of the study, participates in writing study report, develops IDRP (Integrated Data Review Plan) and study site reference guide, formulates requirements for clinical supplies and collaborates on CRF development.Protocol writing, handling amendments, handling study suppies and CRF development is preferred.
GI compound in the Immunology, Transplant and Internal Medicine Department

Key Words: CRA, Clinical Scientist, Protocol, Report, Serious Adverse Events, BSN, RN, Clin*, Pennsylvannia
REQUIREMENTS
MUST HAVE PREVIOUS PHARMACEUTICAL EXPERIENCE