Medical Director, Ild-Ph

The Medical Director, ILD-PH Europe serves as a strategic medical and scientific expert within the organization, responsible for shaping and executing medical affairs strategies that drive therapeutic value, scientific leadership and enrolment in clinical trials.This role provides medical expertise across key medical affairs activities, including healthcare professional engagement, evidence generation (clinical and real-world), scientific communication, medical education, and support of safe and appropriate product use.The Medical Director partners closely with cross-functional teams — including Commercial, Market Access, Regulatory, Safety, and Clinical Development to support the development of Seralutinib in pulmonary hypertension associated with interstitial lung disease.Responsibilities:Provide strategic medical and scientific leadership for Seralutinib in PH-ILD, supporting the development and execution of Medical Affairs plans.Serve as the medical lead for cross-functional product teams, ensuring medical strategy alignment with brand objectives and unmet patient needs.Develop the clinical landscape for PH-ILD in Europe, gain insights into the patient journey, referral patterns, treatment and diagnostic patterns and implement medicalDrive medical evidence generation strategies, including real-world evidence (RWE), observational research, investigator-initiated studies (IIS), and medical affairs-sponsored studies aligned to strategic priorities.Support the dissemination of scientific data through publications, congress presentations, advisory boards, and medical education programs.Provide medical review and approval of promotional and non-promotional materials, ensuring scientific accuracy, fair balance, and compliance with regulatory and ethical standards.Assist in the development of scientifically accurate marketing materials, medical education programs, advisories, and symposia.Assist with the scientific review, development, approval, execution, and communication of affiliate/area/global medical affairs-sponsored or supported clinical research activities.Partner with Commercial, Market Access, Clinical Operations, and Safety teams to provide medical insights and support product development, phase 3 clinical trials, launch readiness, and pre-market activities.Provide medical input into market access and health economics & outcomes research (HEOR) strategies, including value propositions and payer engagement.Coordinate appropriate scientific and medical activities with internal stakeholders (i.e., commercial, clinical operations, discovery, statistics, regulatory, etc.) as they relate to ongoing medical affairs projects.Serve as the scientific team interface for key regulatory discussions.Serve as a therapeutic area expert and resource for internal stakeholders anteamd to the MSLEnsure budgets, timelines, and compliance requirements are factored into programs' scientific activities.Qualifications:Medical Doctorate (M.D.) degree or equivalent (D.O. or non-US equivalent of M.D).Relevant therapeutic specialty in an academic or hospital environment preferred.Completion of residency and/or fellowship is preferred.In-depth understanding of the ILD landscape is a strong preference.Minimum of 2 years of medical affairs experience in the pharmaceutical industry or academia or equivalent.5+ years of experience is preferred.Ability to translate complex scientific information into clear, concise, and impactful medical and strategic guidance is preferred.Knowledge of clinical trial methodology, data analysis and interpretation, regulatory requirements governing clinical trials, and experience in development strategy and the design of protocols.Proven leadership skills in a cross-functional global team environment.Ability to interact externally and internally to support global business strategy.Excellent oral and written English communication skills.This role reports through Gossamer Bio Dublin Ireland office and can be remote within Europe.California Consumer Privacy Act (CCPA) Notice for California Residents:This notice is to notify you that personal data about you has been collected by Gossamer Bio ("Controller"), which is located at **** Merryfield Row, Suite 120, San Diego CA ***** and can be contacted by emailing ****** , because Controller wishes to evaluate your candidacy for employment at Controller.Your personal data was either obtained from publicly available sources (e.g. LinkedIn) or provided to Controller by someone who referred you for potential employment.Controller's Privacy team can be contacted at ****** .Your personal data will be processed for the purposes of managing Controller's recruitment related activities, which include setting up and conducting interviews and tests for applicants, evaluating and assessing the results thereto, and as is otherwise needed in the recruitment and hiring processes.Such processing is legally permissible under Art. 6(1)(f) of Regulation (EU) ******** (General Data Protection Regulation) and the California Consumer Privacy Act (CCPA) as necessary for the purposes of the legitimate interests pursued by the Controller, which are the solicitation, evaluation, and selection of applicants for employment.Your personal data has been shared with Greenhouse Software, Inc., a cloud services provider located in the United States of America and engaged by Controller to help manage its recruitment and hiring process on Controller's behalf.Your personal data will be retained by Controller as long as Controller determines it is necessary to evaluate your application for employment.Under the GDPR and CCPA, you have the right to request access to your personal data, to request that your personal data be rectified or erased, and to request that processing of your personal data be restricted.You also have to right to data portability.In addition, you may lodge a complaint with a supervisory authority.Create a Job AlertInterested in building your career at Gossamer Bio?Get future opportunities sent straight to your email.Apply for this job*indicates a required fieldFirst Name *Last Name *Email *Phone *Location (City) *Resume/CV *Enter manuallyAccepted file types: pdf, doc, docx, txt, rtfDo you hold a Medical Doctorate (M.D., D.O., or non-U.S. equivalent)?* Select...Do you have in-depth knowledge or experience in the ILD (Interstitial Lung Disease) therapeutic area?* Select...How many years of experience do you have in medical affairs (pharma industry, academia, or equivalent)?* Select...This position supports cross-functional global teams across Europe.To help us better understand your ability to communicate effectively in a multilingual environment, please list the languages you are fluent in and indicate your level of proficiency in reading, writing, and speaking for each.*Example format:French – Read: Advanced | Write: Intermediate | Speak: AdvancedAre you based in Europe or able to work remotely in Europe?* 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