Safety Physician

SRG; Valencia; Presencial; EUR 70.000 - 100.000; Jornada completa

Descripción de la vacante

A leading clinical development firm in Valencia is seeking an experienced Safety Physician to provide safety oversight across clinical development programs. This role demands a high level of expertise in clinical safety and pharmacovigilance, with responsibilities including developing risk management plans and preparing key safety documents. The ideal candidate will have an MBBS or MD and at least 7 years of experience in Drug Safety within clinical trials. This position offers a critical role in shaping safety strategy throughout the clinical development lifecycle.

Formación

• 7 years of Drug Safety experience in a clinical trial environment.
• Strong expertise in clinical development projects.

Responsabilidades

• Provide comprehensive safety oversight across development programs.
• Develop and maintain risk management plans and related documentation.
• Collaborate with clinical trial teams on safety topics.

Conocimientos

Clinical Safety and Pharmacovigilance

Signal Detection

Risk Management

Strategic Input

Educación

MBBS or MD

Descripción del empleo

We are currently looking for an experienced Safety Physician to support ongoing and upcoming clinical development projects. This role requires a highly competent professional with strong expertise across Clinical Safety and Pharmacovigilance, contributing both operationally and strategically.

Key Responsibilities

• Providing comprehensive safety oversight across early- and late-stage development programs
• Authoring and reviewing the pharmacovigilance sections of Investigator’s Brochures
• Developing and maintaining risk management plans and associated safety documentation
• Conducting signal detection, evaluation, and ongoing risk management activities
• Supporting responses to questions and requests from global health authorities
• Preparing, reviewing, and contributing to key clinical and safety documents, including CSRs, ICFs, CSPs, IBs, and DSURs
• Performing narrative reviews, evaluation of SAEs and AESIs, database reconciliation, and related safety activities
• Defining and driving safety strategy for early clinical development programs
• Collaborating closely with cross‑functional clinical trial teams on critical safety topics
• Providing strategic input into pharmacovigilance activities and coordinating with both internal teams and external partners

Mandatory Requirements

• Must have MBBS or MD as an educational background.
• Must have 7 years of Drug Safety experience, that in the clinical trial environment.

This role offers the opportunity to play a critical part in shaping and executing safety strategy across the clinical development lifecycle.