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97437 - Clinical Research Specialist II


Job Description:
The incumbent assists with the design and conduct of clinical studies with emphasis on the protocol/TA specific aspects of the protocol. Performs medical monitoring of study data, ensuring appropriate input from clinical research physician and senior clinical research specialist staff. Responsible for the creation, review, and management of SAE case reports. Supports Clinical Sciences and other functional areas in the development of clinical study deliverables. The incumbent will pursue relevant training opportunities and additional project assignments with the goal of assuming increasing autonomy in the execution of responsibilities

Minimum Requirements:
oMust understand scientific process and have familiarity with medical and statistical concepts.
oMust have strong analytic skills and ability to make data driven decisions.
oDesire to work independently and ability to seek guidance as needed.
oMust have good communication (verbal and written) and computer/database management skills.
oExperience as a member/contributor to cross functional teams.

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