(Associate) Medical Director - Rheumatology, EMEA

Thermo Fisher Scientific

Pharmaceutical Industry

Milano - Italien

Director

Hybrid

Experteer Overview

As an Associate Medical Director in our PPD Pharmacovigilance group, you provide medical leadership and expert safety input for clinical trials. You’ll shape protocols, oversee real-time safety monitoring, and serve as the primary medical liaison to sponsors and internal teams. You’ll work cross-functionally to address issues, educate sites, and ensure regulatory compliance. This role offers meaningful impact across global trials and the mission to improve health outcomes.

Responsibilities

Provide medical leadership to study teams and contribute to protocol development and amendments
Oversee real-time medical monitoring to safeguard subject safety and validate primary endpoints
Serve as chief liaison between sponsor and PPD internal departments across study phases
Educate sites through protocol-specific trainings at investigator meetings
Handle day-to-day trial activities, resolve issues, and respond to queries from stakeholders
Ensure study compliance with SOPs and GCP and align medical risks with cross-functional teams
Interact with investigators, IRBs/Health Authorities, and present to study committees as needed
Attend and contribute to investigator meetings and training sessions

Key requirements

Significant experience in pharmaceutical industry and clinical trials
Fluent in English (spoken and written)
Experience with NDA submission process
Understanding of regulatory guidelines for adverse event reporting
Strong communication and presentation skills, good teamwork
Medical Doctor qualification with Rheumatology specialty

strong communication presentation skills teambuilding NDA submission understanding regulatory guidelines for adverse event reporting GCP knowledge

Description

As an Associate Medical Director in our PPD Pharmacovigilance group, you provide medical leadership and expert safety input for clinical tri…

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