Senior Field Clinical Scientist - Neuromodulation
New
United States of America : Remote, East CoastFull-TimeSenior
Salary78000 - 156000 USD per year
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Job Details
- Experience
- Five years in a clinical research environment or other equivalent experience
- Required Skills
- GCP
Requirements
- Four-year degree in Engineering, Biological Sciences, Nursing, or a related field
- Five years in a clinical research environment or other equivalent experience
- Knowledge of regulations and standards (Good Clinical Practices) for conducting clinical research
- Ability to travel domestically and internationally up to 90%
- Polished communicator: written documentation and oral presentations/discussions/meetings
- Ability to work in a highly matrixed and geographically diverse business environment
- Ability to work within a team and as an individual contributor in a fast-paced, changing environment
- Strong verbal and written communications with ability to effectively communicate at multiple levels in the organization
- Multitasks, prioritizes and meets deadlines in timely manner
- Strong organizational and follow-up skills, as well as attention to detail
- Experience and training on GCP
- Minimum 2 years experience as a field clinical specialist or engineer/scientist (Preferred)
- Minimum of 5 years relevant clinical experience in Neuromodulation, Neurological Disorders, Chronic Pain, or Deep Brain Stimulation (Preferred)
- Advanced degree in a relevant discipline/concentration (Preferred)
- Working knowledge of imaging modalities, including x-ray, fluoroscopy and MRI (Preferred)
- Experience with GCP, ISO standards, and clinical trial guidelines (Preferred)
Responsibilities
- Perform discovery visits to access sites for research partnerships
- Complete nomination, qualification, and site activation submissions, visits, and reports
- Ensures site compliance with protocol
- Ensure high quality data collection by attending patient enrollments, key time point follow-up visits, and monitoring visits as appropriate
- Provide protocol and product/procedural training to clinical sites
- Initiate and manage documentable compliance actions
- Conduct regular data quality reviews with principal investigators and research staff
- Assist sites with pre-screening patients to ensure appropriateness for clinical study
- Provide procedural support to ensure safety of subjects in clinical studies
- Assist with registries, new technology assessments, and other special projects as needed
- Train and educate other cross-functional groups on study protocols, therapy areas, and/or clinical research operations
- Provide field perspective to clinical study teams throughout study protocol development and execution
- Partner with regional Sales team by conducting study education and regular site activities updates
- Complies with all applicable local, national, and international regulatory requirements
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