Sign-up for the Sterling-Hoffman Life Sciences Journal to get the latest industry news and job postings.		Job #07242 About our client Our client is a medical device company based in Northern California. They focus on therapies to treat eye diseases. They have 2 regional CRA openings; the right candidate can be based in either the Northeast or the Midwest. Position Location CRA US - Midwest Salary Highly competitive package, commensurate with experience Responsibilities 1) Perform and coordinate all aspects of the clinical monitoring process in accordance with GCPs and global SOPs 2) Assess safety and efficiency of investigational products and/or medical devices 3) Represent client in the global medical research community 4) Develop collaborative relationships with investigative sites and client company personnel Requirements 1) Bachelor's degree in life sciences or related field or certification in a related allied health profession from an appropriately accredited institution (RN, MT, PA, RPh or RT) 2) Minimum 2 years of experience as a Clinical Monitor 3) Experience with electronic data capture a plus 4) Experience with ophthalmology a plus 5) Demonstrated ability to attain and maintain a working knowledge of GCPs and applicable SOPs 6) Effective clinical monitoring skills 7) Demonstrated understanding of medical terminology 8) Basic computer skills and ability to learn and become proficient with appropriate software 9) Effective oral and written communication skills with ability to communicate effectively with medical personnel 10) Ability to work in a team environment and independently as needed 11) Strong customer focus and excellent interpersonal skills 12) Strong attention to detail 13) Proven flexibility and adaptability 14) Ability to qualify for and maintain a corporate credit card with sufficient credit line to allow for extensive business travel 15) Valid driving license 16) Ability and willingness to travel (up to 60 – 70%)
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