(Associate) Medical Director - Neurology

Thermo Fisher Scientific

Pharmaceutical Industry

Milano - Italien

Director

Hybrid

Experteer Overview

In this role you will provide medical leadership for clinical trials within Pharmacovigilance, ensuring medical validity and safety across study phases. You will collaborate with cross-functional teams to develop protocols, oversee study documentation, and monitor real-time safety signals. You will act as a key medical liaison with sponsors, sites, and regulators, shaping trial conduct and training site staff. This is an opportunity to influence patient safety and trial quality at a global scale while working with a diverse, mission-driven organization.

Responsibilities

Provide medical leadership to study teams and contribute to protocol development, site selection, and review/approval of study documents (protocols, amendments, CSRs, ICFs, CRFs)
Perform real-time medical monitoring to ensure safety and validity of primary endpoints; identify issues early
Collaborate with Global Medical Indication Lead to address customer concerns and implement corrective actions
Lead initial protocol reviews with internal groups on procedural and budgetary items and changes due to amendments
Serve as chief liaison between sponsor and internal departments across study phases
Educate investigator sites through protocol-specific lab procedures presentations at investigator meetings
Manage day-to-day trial activities to resolve issues and respond to queries
Act as medical point of contact for internal/external stakeholders; interact with investigators, IRBs, Health Authorities; provide training to site staff
Ensure study compliance with SOPs and GCP; maintain cross-functional collaboration to clarify medical risks and results

Key requirements

MD, MB/BS or equivalent
significant experience in pharmaceutical industry and clinical trials
fluency in spoken and written English
experience with NDA submission process
understanding regulatory guidelines for adverse event reporting
strong communication and presentation skills
team player with cross-functional collaboration abilities
experience in Neurology or Epileptology is advantageous

strong communication presentation skills team collaboration NDA submission process GCP and SOP compliance adverse event reporting guidelines

Description

In this role you will provide medical leadership for clinical trials within Pharmacovigilance, ensuring medical validity and safety across s…

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