Senior Medical Writer & Project Lead

IQVIA

Madrid

Presencial

EUR 90.000 - 130.000

Jornada completa

Hace 12 días
Generador de candidaturas

Convierte este puesto en una entrevista — un currículum y una carta de presentación creados pensando en lo que quiere el empleador.

Supera los filtros ATS

Descripción de la vacante

IQVIA is seeking a Lead Medical Writer to act as the primary author on medical writing projects and ensure adherence to SOPs and customer requirements. The role includes senior review, timeline negotiation, and direct communication with customers.

You will mentor junior staff, stay updated on regulatory knowledge, and contribute to cross-functional initiatives within a global team. This is a senior role with leadership responsibilities across projects.

Formación

  • Bachelor's degree in life sciences or related field.
  • Master's degree in life sciences recommended.
  • Ph.D. in life sciences preferred.
  • Typically requires at least 5 years of relevant experience.
  • Knowledge of CSR, protocol-writing, and regulatory standards.
  • Good understanding of statistical methods in clinical trials.
  • Ability to review SAP and identify deficiencies in outputs.
  • Strong written and oral communication with customers and project managers.
  • Ability to manage multiple tasks and negotiate timelines.

Responsabilidades

  • Lead preparation of assigned documents, confirm scope, templates, specs, and timelines.
  • Plan workload, track timelines, and implement customer requests.
  • Lead meetings on challenging topics independently.
  • Present on Medical Writing processes at bid defense meetings.
  • Mentor/train junior staff and deliver training to global teams.

Conocimientos

Medical writing leadership
CSR/Protocol expertise
GCP knowledge
Budgeting/Finance
Mentoring
Client communication
Project management

Educación

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

Herramientas

Microsoft Office
Statistical software

Descripción del empleo

IQVIA is seeking a Lead Medical Writer to act as the primary author on medical writing projects and ensure adherence to SOPs and customer requirements. The role includes senior review, timeline negotiation, and direct communication with customers.

You will mentor junior staff, stay updated on regulatory knowledge, and contribute to cross-functional initiatives within a global team. This is a senior role with leadership responsibilities across projects.

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