Clinical Research Specialist II - Cardiovascular

A large pharmaceutical company is looking for a Clinical Research Specialist - II (Associate) with Cardiovascular experience.

Responsibilities:Assists with the design and conduct of clinical studies with emphasis on the protocol/TA specific aspects of the protocolPerforms 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 Serious Adverse Events (SAE) case reportsSupports Clinical Sciences and other functional areas in the development of clinical study deliverablesThe incumbent will pursue relevant training opportunities and additional project assignments with the goal of assuming increasing autonomy in the execution of responsibilitiesThe individual will work in the CRS Safety Group processing and reviewing serious adverse experiences in a clinical study setting

Qualifications:Must understand scientific process and have familiarity with medical and statistical conceptsMust have strong analytic skills and ability to make data driven decisionsDesire to work independently and ability to seek guidance as neededMust have good communication (verbal and written) and computer/database management skillsExperience as a member/contributor to cross functional teamsDegree in Life Science/Medical requiredCardiovascular experience a plus