Siemens Healthcare Private Limited Hiring Medical Affairs
Specialist Master’s in medical technology, laboratory science, chemical,
physical, or biological science Apply Now
Specific Responsibilities
Primarily responsible for contributing to the timely
completion of various health risk assessments and clinical use related
evaluations of LD products.
Reports directly to Siemens LD Medical Affairs
Key Job Attributes
A. Within specific job description:
1. Works independently or as part of a larger team in
the execution of assigned projects.
2. Maintains accurate documentation and files related
to all activities and tasks.
3. Interacts directly within cross-functional teams
and builds productive cross-functional working relationships for the completion
of assigned tasks.
4. Critically reviews analytical and clinical
performance data and reports and provides assessment of clinical/medical impact
and/or risk.
B. Critical Problem Thinking:
1. Applies a strong clinical laboratory background to
assess the application of medical laboratory test results (e.g. biomarkers) in
clinical practice.
2. Translates and integrates the latest clinical
guidance and guidelines for the use of laboratory biomarkers in the care of
patients, including assessment of the impact of laboratory results on
diagnosis, monitoring and treatment.
3. Demonstrates understanding of intended clinical use
of complex in vitro diagnostic laboratory medical devices.
4. Displays an expert level of critical thinking in
applying principles of clinical laboratory medicine, including analytical
laboratory practice (e.g. assay validation, quality control) and regulations,
to patient care applications.
5. Proactive attitude with logical, data driven
approach to problem solving.
6. Performs special assignments and provides technical
and clinical advice in area of expertise.
C. Education (Description is US-based; equivalent for
India required):
M.D., Ph.D. or M.D./Ph.D. in related areas with
practical experience in clinical pathology preferred. Equivalent combination of
relevant education and experience, such as Master’s in medical technology,
laboratory science, chemical, physical, or biological science AND a minimum of
3 years of medical laboratory experience in clinical consultancy and technical
and regulatory oversight, as outlined above, may be substituted as appropriate.
Board certification and ongoing accreditation by nationally and internationally
known professional clinical and academic bodies such as ABCC, NRCC, CACB, RCP,
ABP preferred.
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