Oncology Medical Director — Clinical Trials Leader

IQVIA

Milano

In loco

EUR 99.000 - 168.000

Tempo pieno

14 giorni+
Generatore di candidature

Una candidatura apposita per questo posto — un curriculum e una lettera di presentazione personalizzati, perfettamente in linea con l'annuncio.

Supera i filtri ATS

Descrizione del lavoro

IQVIA is seeking a Medical Director to provide medical and scientific oversight for clinical trials conducted by IQVIA Biotech Clinical on behalf of sponsor companies. The Medical Director serves as the primary medical monitor and is available 24/7 to support protocol questions and patient safety.

You will collaborate with project teams, review data, ensure GCP compliance, and contribute to protocol development, SAE reviews, and safety reporting.

Competenze

  • Medical Degree from an accredited school.
  • 10 years of experience in medical practice, academia, clinical research, or drug development.
  • 3-5 years of biopharmaceutical (industry) experience preferred.
  • Ability to work in partnership with a multidisciplinary group in a matrix environment.
  • Excellent oral and written communications skills.

Mansioni

  • Provide medical oversight as Medical Monitor for IQVIA Biotech Clinical studies for sponsor companies.
  • Serve as primary contact for sponsor medical team and support project teams.
  • Ensure medical activities comply with GCP and operate efficiently.
  • Interact with clients regarding drug development programs and protocol input.
  • Develop and review protocol development, safety reporting, and SAE narratives.
  • Provide on-call coverage for protocol queries and site support.

Conoscenze

Communication skills
Team collaboration
Independent work
Project management

Formazione

Medical Degree

Descrizione del lavoro

IQVIA is seeking a Medical Director to provide medical and scientific oversight for clinical trials conducted by IQVIA Biotech Clinical on behalf of sponsor companies. The Medical Director serves as the primary medical monitor and is available 24/7 to support protocol questions and patient safety.

You will collaborate with project teams, review data, ensure GCP compliance, and contribute to protocol development, SAE reviews, and safety reporting.

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