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2 дня назад

Medical Information Representative (Pharmaceutical Medical Information)

67 500 - 80 000$
Формат работы
onsite
Тип работы
fulltime
Английский
b2
Страна
US
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

Текст:
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TL;DR
Medical Information Representative (Clinical & Medical): Responding to unsolicited medical information requests and managing adverse event and product complaint reports for pharmaceutical products with an accent on clinical evaluation, evidence-based communication, and regulatory compliance. Focus on researching medical literature, documenting safety cases, coordinating quality-related complaints, and delivering accurate support across phone, email, CRM, and chat channels.

Location: Overland Park, Kansas, USA; office-based role with full-time scheduling and up to 10% travel.

Salary: USD 67,500–80,000 per year

Company

hirify.global provides commercialization services, products, and solutions for life sciences companies and supports pharmaceutical and biotech clients worldwide.

What you will do

  • Respond independently to unsolicited medical information inquiries from healthcare professionals, patients, caregivers, and payers.
  • Research and critically evaluate medical literature to prepare scientifically balanced, evidence-based responses.
  • Identify, document, and report adverse events and product complaints in accordance with company and client procedures.
  • Handle requests across phone, email, CRM, chat, and other communication platforms.
  • Coordinate product quality complaint processes with Quality Assurance, Regulatory Affairs, and complainants.
  • Maintain product and therapeutic-area knowledge while supporting multiple pharmaceutical clients.

Requirements

  • Associate, bachelor's, or master's degree in nursing or a related healthcare discipline.
  • Strong clinical or healthcare background with the ability to interpret and communicate medical information clearly and accurately.
  • Excellent verbal and written communication skills and the ability to work independently and collaboratively.
  • Availability for full-time work of 40 or more hours per week, typically Monday through Friday, with scheduling flexibility.
  • Knowledge of FDA post-marketing adverse event reporting regulations and safety terminology.
  • Ability to work in an office environment, including prolonged sitting or standing and occasional lifting of up to 25 pounds.

Nice to have

  • Advanced healthcare degree or equivalent qualification.
  • Registered Nurse license or equivalent licensure.
  • At least two years of experience in healthcare, clinical practice, the pharmaceutical industry, or a related field.
  • Direct clinical or patient-facing experience, contact center experience, and proficiency with medical information databases, telephony, Microsoft Office, and video conferencing platforms.
  • Experience in drug information or therapeutic areas such as oncology, hematology, immunology, rare disease, neurology, or cardiology.

Culture & Benefits

  • Patient-focused work supporting the safe and effective use of pharmaceutical products.
  • Commitment to diversity, equity, and inclusion.
  • Opportunities to contribute to process improvement and clinical customer service quality.
  • Participation in scientific medical affairs booths and assigned on-call coverage.
  • Reasonable workplace and hiring-process accommodations are available for qualified individuals with disabilities.

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