We are an innovative Medical Device Company with an IMMEDIATE Full time job opening for a Senior Biomedical Researcher.
To conceive, develop and execute innovative R&D applicable to new medical devices via advanced signal processing and algorithm development, and to contribute in securing R&D grant funding.
Duties and Responsibilities:
Conceive new ideas within Company's mission statement and write grant proposals to the NIH, DOD and other funding agencies.
Execute/administer funded R&D programs, both independently and collaboratively. Interface as needed with funding agencies and program officials.
Develop and implement novel signal processing/analysis algorithms in MATLAB for patient/subject monitoring and aid in diagnosis/therapy based on physiological signals such as electroencephalogram (EEG).
Design clinical studies to acquire bio/physiological signals from human subjects for algorithm development and validation.
Develop and validate algorithms based on acquired human subjects/clinical data.
Perform statistical analysis of acquired and processed data.
Develop and maintain regulatory documentation for related clinical studies (Trial Master File and Study Site File) as per current Good Clinical Practice (cGCP).
Participate as needed in training, monitoring and audits of clinical sites.
Prepare scientific reports and publications. Present at scientific conferences.
Provide support for intellectual property protection.
Provide support for EU/FDA regulatory submissions.
Perform any other related duties as assigned.
Travel (incl. international) may be needed.
Education and Skills:
MS (or PhD) or equivalent, in biomedical engineering, electrical/computer engineering, or related fields. PhD is desired.
Theoretical knowledge and practical experience in biomedical research, particularly in advanced Digital Signal Processing/analysis.
Proven track record in conception and implementation of innovative algorithms for extraction of relevant information/features from signals/data.
Proficient in programming in MATLAB.
Excellent oral/verbal/written communication skills in English.
Experience with writing scientific publications.
Experience with writing grant proposals is desired.
Experience with analysis of bio/physiological signals is desired.
Experience with statistical analysis of data is desired.
Experience in cGCP and medical device industry regulation is desired.
Please email your cover letter and resume (with salary requirements) to our HR Department.
Employment Type: Permanent
Work Hours: Full Time
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