(Associate) Medical Director Pulmonology, EMEA

Overview (Associate) Medical Director Pulmonology, EMEA – Thermo Fisher Scientific Join to apply for the role at Thermo Fisher Scientific. Work Schedule: Standard (Mon-Fri) Environmental Conditions: Office Responsibilities Provide medical leadership to the study teams, including creating clinical trial protocols while implementing the latest scientific information; contribute to site selection; review and approval of study protocols and amendments, Clinical Study Reports (CSRs), Informed Consent Forms (ICFs), Case Report Forms (CRFs), protocol deviation decisions and other clinical documents as required for the conduct of clinical trials. Real-time medical monitoring of clinical studies: ensure medical validity of each primary endpoint and subject safety; identify medical issues early; pro-active customer concern and correction of issues in consultation with the Global Medical Indication Lead. During initial protocol review, consult with internal groups regarding procedural and budgetary items and the necessity for changes due to amendments; coordinate with other functions to close gaps and address issues timely; serve as chief liaison between sponsor and PPD internal departments; educate Investigator sites by delivering protocol-specific lab procedures presentations during investigator meetings; manage day-to-day activities to resolve issues and answer queries. Act as medical point of contact for internal and external stakeholders: interact with investigators, answer questions from IRBs and Health Authorities, prepare and present material to the study executive and independent safety committee if applicable; provide medical training of site staff at Investigator meetings; CRA training in new indications. Ensure study compliance for all medical aspects by understanding and applying relevant SOPs and GCP. Collaborate with cross-functional study team members to ensure medical risks, issues, and results are clearly communicated to all involved parties. Qualifications MD, MB/BS or equivalent degree with strong medical knowledge; clinical experience in running Pulmonology patients in hospital practice. Significant experience within pharmaceutical industry, clinical trials and pharmaceutical medicine. Fluent in spoken and written English. Experience with NDA submission processes and regulatory guidelines for adverse event reporting. Strong communication and presentation skills; proven ability to work well in a team. Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status. J-18808-Ljbffr

Location: Milano, Lombardia, IT

Posted Date: 9/17/2025