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Medical Manager - Genitourinary Oncology

Формат работы
remote (только Mexico)
Тип работы
fulltime
Грейд
middle
Английский
c1
Страна
Mexico
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
Для мэтча и отклика нужен Plus

Мэтч & Сопровод

Для мэтча с этой вакансией нужен Plus

Описание вакансии

Текст:
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TL;DR
Medical Manager - Genitourinary Oncology (Medical Affairs/Clinical Research): Managing medical affairs, clinical research, regulatory activities, and scientific engagement for genitourinary oncology products in Mexico with an accent on clinical collaborations, pharmacovigilance, compliance, and medical strategy. Focus on coordinating locally sponsored trials, preparing risk management plans, supporting product registrations, and developing evidence-based educational and promotional materials.

Location: Remote in Mexico

Company

hirify.global is a pharmaceutical company developing and providing medicines supported by medical, clinical research, regulatory, and pharmacovigilance functions.

What you will do

  • Provide medical and scientific support for assigned genitourinary oncology products to internal and external stakeholders while ensuring compliance with hirify.global procedures and applicable regulations.
  • Develop and execute the local Medical Affairs plan, manage the annual budget, support product launches, and provide scientific input for promotional materials and medical education programs.
  • Lead clinical and research collaborations, locally sponsored interventional and non-interventional studies, compassionate access programs, and related timelines and budgets.
  • Coordinate risk management plans, post-authorization safety studies, medical information, adverse-event follow-up, audits, inspections, and CAPA activities.
  • Support regulatory submissions, product registrations, local product documents, package inserts, formularies, listings, and new therapeutic indication dossiers.
  • Build relationships with key opinion leaders, medical societies, academic institutions, health authorities, and investigators while coaching MSLs and training commercial colleagues.

Requirements

  • Medical degree required; a specialty is preferred, with medical knowledge in the assigned therapeutic area.
  • At least 3 years of experience in clinical practice, medical affairs, R&D, medical marketing, marketing, clinical research, or medical direction, preferably in the pharmaceutical industry.
  • Fluent written and spoken English required.
  • Knowledge of local regulations and the scientific, ethical, regulatory, and legal requirements for human clinical research.
  • Experience with project and budget administration and management.
  • Strong presentation, public speaking, teaching, negotiation, communication, strategic thinking, planning, leadership, and decision-making skills; business travel is required.

Culture & Benefits

  • Work is performed remotely from Mexico.
  • Emphasis on integrity, innovation, respect for people, customer focus, teamwork, leadership, performance, and community.
  • Participation in required training, inspection-readiness activities, corporate audits, and regulatory inspections.
  • Inclusive working environment that encourages open discussion, debate, colleague development, and effective change management.

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