Lead Medical Writer & Strategic Project Manager

IQVIA

Lisboa

Presencial

EUR 76 000 - 111 000

Tempo integral

Há 7 dias
Torna-te num dos primeiros candidatos
Gerador de candidaturas

Uma candidatura completa num minuto — currículo personalizado e carta de apresentação, prontos a enviar.

Ultrapassa os filtros ATS

Resumo da oferta

IQVIA is seeking a Lead Medical Writer to act as the primary writer on complex documents, ensuring alignment with SOPs and customer requirements. You will lead review cycles, negotiate timelines, and ensure high-quality deliverables across global teams.

The role involves mentoring junior staff, presenting at bid defenses, and may include project management and budgeting duties to support senior leadership in a regulated environment.

Qualificações

  • Lead writer with CSR and protocol experience.
  • Strong knowledge of GxP and regulatory writing standards.
  • Identify deficiencies and ensure accuracy in reports.
  • Excellent written and oral communication skills.
  • Ability to manage multiple tasks and projects.

Responsabilidades

  • Lead the preparation of documents, confirm scope, templates, timelines, and coordinate reviews.
  • Plan workload, track timelines, and implement customer requests.
  • Lead meetings on challenging topics.
  • May present Medical Writing processes at bid defense meetings.
  • Mentor junior staff and deliver global training.
  • Possibly act as Project Manager including Finance/Invoicing.
  • Complete project finance activities and forecast hours.
  • Propose and approve budgets for routine projects.
  • May take on a small customer lead role.
  • Represent region or site on initiatives.
  • Facilitate ideas and participate in capabilities audits.

Conhecimentos

Lead writer
Regulatory writing
Project management
Client interaction
Mentoring

Formação académica

Bachelor's Degree in life sciences
Master's Degree
Ph.D. in life sciences

Descrição da oferta de emprego

IQVIA is seeking a Lead Medical Writer to act as the primary writer on complex documents, ensuring alignment with SOPs and customer requirements. You will lead review cycles, negotiate timelines, and ensure high-quality deliverables across global teams.

The role involves mentoring junior staff, presenting at bid defenses, and may include project management and budgeting duties to support senior leadership in a regulated environment.

Obtém a tua avaliação gratuita e confidencial do currículo.

ou arrasta e larga o ficheiro aqui.

Similar jobs

Ofertas semelhantes que vale a pena comparar

Lead Medical Writer & Project Lead
Lead Medical Writer & Project Lead

IQVIA • Oeiras

Presencial
EUR 60 000 - 90 000
Senior Medical Writer & Project Lead
Senior Medical Writer & Project Lead

IQVIA Argentina • Oeiras

Presencial
EUR 98 000 - 124 000
Principal Medical Writer - FSP
Principal Medical Writer - FSP

IQVIA • Oeiras

Presencial
EUR 60 000 - 90 000
Principal Medical Writer - FSP
Principal Medical Writer - FSP

IQVIA • Lisboa

Presencial
EUR 76 000 - 111 000
Senior Medical Writer: Clinical Docs Lead for Eye Health
Senior Medical Writer: Clinical Docs Lead for Eye Health

IQVIA • Lisboa

Presencial
EUR 45 000 - 65 000
Associate Director, Global Regulatory Strategy
Associate Director, Global Regulatory Strategy

IQVIA • Oeiras

Presencial
EUR 150 000 - 190 000
Senior/ Medical Writer - FSP (M/W/D)
Senior/ Medical Writer - FSP (M/W/D)

Iqvia • Lisboa

Presencial
EUR 45 000 - 65 000
Global Regulatory Strategy Lead
Global Regulatory Strategy Lead

IQVIA LLC • Porto

Híbrido
EUR 90 000 - 130 000
Associate Director, Regulatory Affairs
Associate Director, Regulatory Affairs

IQVIA LLC • Porto

Presencial
EUR 90 000 - 130 000
Global Medical Safety Director: Strategy & Leadership
Global Medical Safety Director: Strategy & Leadership

Iqvia Argentina • Viseu

Presencial
EUR 90 000 - 120 000