Medical Information Manager — Immunology & Drug Info Expert

ADMA Biologics, Inc.

Boca Raton (FL)

On-site

USD 110,000 - 140,000

Full time

14 days+

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Benefits offered by this job

401K plan with employer match and vest
Medical, Vision, Life and Dental
Pet Insurance
Company paid STD and LTD
Company Paid Holidays
3 Weeks' Paid Time Off
Tuition Assistance
Shuttle service to Boca Tri-Rail

Job summary

ADMA Biologics, a biopharmaceutical company in Boca Raton, seeks a Manager, Medical Information to serve as a product and disease state expert within Medical Affairs. You will provide medical, scientific and technical support for product communications and field Medical Science Liaison teams.

Responsibilities include creating and reviewing medical information content, developing materials, coordinating with Compliance and Clinical Development, and supporting promotional claims with data-File

Qualifications

  • PharmD, RPh, RN, PhD or similar required.
  • Experience in pharmaceutical industry, drug information.
  • Strong writing and time management skills.
  • Immunology/Respiratory/Infectious disease background a plus.
  • Compliant with FDA regulations.

Responsibilities

  • Create and review medical information content for ADMA products.
  • Develop, review and maintain Medical Affairs materials.
  • Collaborate on training materials for Medical Affairs and liaise with internal stakeholders.
  • Coordinate development, review and approval of Data on File packets to support claims.
  • Support field Medical Science Liaisons with scientific information.

Skills

Medical information
Writing
Time management
Call center experience
Immunology
Respiratory disease
Infectious disease

Education

PharmD/RPh/RN/PhD

Job description

ADMA Biologics, a biopharmaceutical company in Boca Raton, seeks a Manager, Medical Information to serve as a product and disease state expert within Medical Affairs. You will provide medical, scientific and technical support for product communications and field Medical Science Liaison teams.

Responsibilities include creating and reviewing medical information content, developing materials, coordinating with Compliance and Clinical Development, and supporting promotional claims with data-File

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