(Associate) Medical Director - Oncology, Emea Lisboa

(Associate) Medical Director - Oncology, Emea
Lisboa
Lisboa, Lisboa, Portugal

Overview

(Associate) Medical Director Pulmonology, EMEA – Join to apply for the

(Associate) Medical Director Pulmonology, EMEA

role at

Thermo Fisher Scientific. Work Schedule: Standard (Mon-Fri). Environmental Conditions: Office. At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Our work spans laboratory, digital and decentralized clinical trial services in a global portfolio. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on now and in the future. Responsibilities

Provide medical leadership to the study teams, including creating clinical trial protocols while implementing the latest scientific information, contribute to site selection, involved in 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 individual primary endpoint as well study subject safety, while ensuring medical issues are identified early. Pro-active customer concern and correction of issues in consultation with the Global Medical Indication Lead
During initial review of protocol, consults with internal groups and support staff regarding procedural and budgetary items and the necessity for change due to any subsequent protocol amendments. Acquires other functions’ dedication to close gaps and address issues timely and effectively. Serves as chief liaison between sponsor and all PPD internal departments performing the required tasks during all study phases. Educates Investigator sites by delivering a protocol specific lab procedures presentation and demonstration during an investigator meeting. Controls, handles and follows day to day activities during the course of the clinical trial to resolve any issues and answer queries
Medical point of contact for all internal and external stakeholders: Interact with the investigators as needed, answer questions of IRBs and Health Authorities, prepare and present material to the study executive and independent safety committee if applicable;



medical training of site staff at Investigator meetings;



CRA training in new indications
Ensure study compliance for all medical aspects by understanding and applying all relevant SOPs and GCPClosely collaborate with the cross functional study team members in order for medical risks, issues, and results to be clear to all involved parties
Qualifications

Education: MD, MB/BS or equivalent degree and strong medical knowledge, shown clinical experience running Pulmonology patients in hospital practice
Knowledge, Skills, Abilities: Significant experience within pharmaceutical industry, clinical trials and pharmaceutical medicine;



fluent in spoken and written English;



understanding andexperience with NDA submission process;



understanding of regulatory guidelines for adverse event reporting;



strong communication & presentation skills and is a strong teammate
Our Mission is to enable our customers to make the world healthier, cleaner and safer.

Apply today!

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.

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