Researcher, Prin Clin - 100211 - Valencia, CA - 0300

Biotechnology and Pharmaceutical Researcher, Prin Clin - 100211 - Valencia, CA - 0300 Job Description:(ORC Job Code: T471) Develops and maintains liaison among outside physicians, preclinical and clinical investigators, medical educators, and department heads in medical schools, CRO's, affiliated hospitals, state and/or government hospitals, and research institutions to initiate and expedite clinical studies on products that have investigational new drug (IND) or 510k approval. Contacts and recommends qualified investigators to perform studies, prepare exhibits, and provide scientific and medical consultations for any phase of development studies. Responsible for administrative duties such as reviewing cases with investigators, determining and monitoring time schedules, preparing investigator packets, and issuing status reports. Assists with design, development, and monitoring of clinical evaluation projects. Includes inside and outside CRAs. (SIRS Job Level: Technical Level 4) Applies extensive technical expertise, and has full knowledge of other related disciplines. Develop technical solutions to complex problems which require the regular use of ingenuity and creativity. Work is performed without appreciable direction. Exercises considerable latitude in determining technical objectives of assignment. Completed work is reviewed from a relatively long- term perspective, for desired results. Guides the successful completion of major programs and may function in a project leadership role. Erroneous decisions or recommendations would typically result in failure to achieve major organizational objectives. Represents the organization as the prime technical contact on contracts and projects. Interacts with senior external personnel on significant technical matters often requiring coordination between organizations.Job Experience:Develops and maintains liaison among outside physicians, preclinical and clinical investigators, medical educators, and department heads in medical schools, CRO's, affiliated hospitals, state and/or government hospitals, and research institutions to initiate and expedite clinical studies on products that have investigational new drug (IND) or 510k approval. Contacts and recommends qualified investigators to perform studies, prepare exhibits, and provide scientific and medical consultations for any phase of development studies. Responsible for administrative duties such as reviewing cases with investigators, determining and monitoring time schedules, preparing investigator packets, and issuing status reports. Assists with design, development, and monitoring of clinical evaluation projects. Includes inside and outside CRAs. (SIRS Job Level: Technical Level 4) Applies extensive technical expertise, and has full knowledge of other related disciplines. Develop technical solutions to complex problems which require the regular use of ingenuity and creativity. Work is performed without appreciable direction. Exercises considerable latitude in determining technical objectives of assignment. Completed work is reviewed from a relatively long- term perspective, for desired results. Guides the successful completion of major programs and may function in a project leadership role. Erroneous decisions or recommendations would typically result in failure to achieve major organizational objectives. Represents the organization as the prime technical contact on contracts and projects. Interacts with senior external personnel on significant technical matters often requiring coordination between organizations.Minimum Education Required: BachelorYears of Experience Required: 3-5 YearsExpected Travel Time: NoneThis company may offer relocation assistance. Please visit us online at www.bostonscientific.com for more information.