CLINICAL RESEARCH SPECIALIST/ CLINICAL RESEARCH ASSOCIATE

A World Leader in Medical Technology is seeking a Clinical Research Associate to work an in-house position at their Northridge, California location.

Compensation is commensurate with experience and education.

Job Duties: Assists with successful conduct of assigned studies consistent with R&D and Marketing plans. Assists in preparation of study materials and training of investigators, center staff and Medtronic field staff. Writes monitoring plans. Coordinates and conducts monitoring at participating centers to ensure compliance with the protocol and regulations and the timely receipt of accurate data and other required study documents. Reviews clinical data/information and oversees data correction. Assists study managers in providing interim and final reports and presentations. Provides input to study budgets and project plans. Assists study manager in writing PMA Clinical Reports. Reviews and approves center activation documents. Work with the Clinical Study Manager to satisfy applicable regulatory standards. Evaluates and analyzes clinical data.,Oversees, designs, plans, develops and monitors clinical evaluation projects. Establish the conditions essential for determining the safety, efficacy, medical usefulness and marketability of drug or medical device and product candidates.

Qualifications:
> Bachelor Degree or higher
> 5 years experience as a CRA
> Strong communication skills
> Ability to travel up to 25-50%