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Senior Medical Manager, Catheter Care.

Apply Now Job ID R-347318 Date posted 09/13/2019

Job Description Summary

Job Description

Reporting to the WW Director, Medical Affairs (MA) this position has the responsibility to provide medical, scientific, technical and customer-focused support. Provides guidance from a medical perspective to value maximization of current and future products and processes for the respective platforms.

Responsible for enhancing scientific relationships with Key Opinion Leaders (KOLs), reviewing promotional and educational material for accuracy; leading consultant and advisory meetings; and reviewing grant applications for scientific merit.

Responsibilities:

  • Contribute to the development and implementation of clinical research and educational projects in areas of interest globally; participate in the development of plans for future clinical studies.
  • Guide design of clinical trials and registries globally. Ensure support for activities in clinical development by collaborating with the clinical operations group.
  • Direct the distribution of scientific and medical information to internal and external customers while meeting appropriate legal and regulatory guidelines.
  • Co-develop appropriate strategic go-to-market models with business group and commercial teams.
  • Direct the identification and development of KOLs across different therapy areas as needed, investigate new uses of BD’s products, and ensure collaboration with appropriate scientific societies.
  • Participate as needed as part of the crisis-management teams for marketed products, i.e. in case of field corrective actions.
  • Ensure relevant and appropriate responses to customer inquiries for relevant BD products.
  • Direct the regular review of scientific literature in cooperation with marketing for key-products.
  • Continuously maintain “state of the art” level of knowledge for the medical and commercial teams as to developments and trends in medical science relevant to the business.
  • Be part of an environment that stresses open, candid, and timely feedback relative to performance.
  • Continuously develop knowledge of regulatory, pharmacovigilance and quality assurance requirements in alignment with BD Practice Standards.

Qualifications:

  • Minimum BS RN plus previous management experience is required.
  • At least 5 years related experience in the medical device or pharmaceutical industry within clinical research or medical affairs is preferred.
  • 3-5 years of medical practice required
  • Clinical trial experience with solid knowledge of Good Clinical Practice (GCP).
  • Demonstrated ability to present complex issues in oral and written form.
  • Demonstrate strong business acumen and critical thinking skills.
  • Process-oriented and demonstrates a sense of urgency in completing deliverables through effective goal setting and a strong result orientation.
  • Must be able to organize, prioritize and work effectively in a constantly changing environment
  • Excellent written, oral communication and computer software skills. Excellent presentation skills of scientific and medical data to small and large audiences.
  • Knowledgeable in the areas of regulatory, commercial and clinical issues affecting the pharmaceutical /medical device industry. 
  • Demonstrate ability to identify unmet clinical needs, evaluate product opportunities from a clinical perspective, and help develop strategies that leads to efficient development of such opportunities.
  • Working knowledge of safety reporting requirements for both drugs and devices.
  • Ability and willingness to travel 20-30% of time.

#LI-TECH

Primary Work Location

USA NJ - Franklin Lakes

Additional Locations

Work Shift

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