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6 дней назад

Medical Information Specialist (Biotechnology)

6 154 - 7 827$
Формат работы
remote (только USA)
Тип работы
fulltime
Грейд
middle
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 Specialist (Biotechnology): Managing medical information operations and responding to healthcare professional, patient, caregiver, investigator, and consumer inquiries about ANKTIVA and clinical trials with an accent on medical communications, safety information, and regulatory compliance. Focus on writing standard and custom medical responses, triaging adverse events and product complaints, confirming trial eligibility, and maintaining accurate inquiry documentation.

Location: Remote within the United States; Monday–Friday during standard business hours, with flexibility subject to manager approval. Possible travel of up to one day per month.

Salary: $6,154–$6,769 biweekly in national markets; $7,115–$7,827 biweekly in premium markets including Los Angeles, San Diego, San Francisco, New York City, Chicago, and Boston.

Company

hirify.global is a publicly traded biotechnology company developing immunotherapies, cell therapies, vaccines, and next-generation treatments for cancer and infectious diseases.

What you will do

  • Respond to and resolve escalated medical and safety inquiries from healthcare professionals, patients, caregivers, investigators, and other external customers.
  • Write and update standard response documents, custom medical information responses, standard operating procedures, and medical communications materials.
  • Provide accurate labeled and unlabeled efficacy, safety, scientific, and product information in accordance with regulatory requirements and industry standards.
  • Identify, document, and report adverse events, special situation events, and product complaints to Pharmacovigilance.
  • Review clinical trial eligibility and connect patients or caregivers with appropriate trial contacts.
  • Track inquiries, troubleshoot medical information database issues, and generate operational metrics and reports.

Requirements

  • Advanced scientific degree required: PharmD, MD, or PhD.
  • At least 2 years of pharmaceutical Medical Affairs industry experience and 2 years of Medical Information and Medical Communications Operations experience.
  • Professional experience with call center operations, medical information inquiry tracking, Standard Response Letter writing, and medical operations policies.
  • Working knowledge of medical terminology, pathophysiology, pharmacology, regulations, industry standards, HIPAA, and federal guidelines.
  • Strong written and verbal communication skills, discretion with confidential information, sound judgment, collaboration, and customer-service orientation.
  • Proficiency in Microsoft Office and the ability to manage multiple priorities in a fast-paced environment.

Nice to have

  • Experience with Veeva Vault Promomats and medical information databases.
  • Oncology experience, particularly in prostate, bladder, lung, glioblastoma, or colorectal cancer.

Culture & Benefits

  • Collaborative environment with opportunities to work across different areas of the company.
  • Professional development opportunities in a growing biotechnology company.
  • Medical, dental, and vision plan options, health and financial wellness programs, and an Employee Assistance Program.
  • Life, disability, flexible spending, retirement, education, legal, identity protection, pet insurance, and employee discount benefits.
  • Paid time off, holidays, and additional health, personal, and cultural leave depending on employee classification.

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