Medical Director – Dermatology

🔥 22 minutes ago

🇦🇷 Argentina – Remote

⏰ Full Time

🟠 Senior

👨‍⚕️ Medical Director

👻 Ghost score 12%

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Thermo Fisher Scientific

WebsiteLinkedInAll Job Openings

10,000+ employees

🧬 Biotechnology

💊 Pharmaceuticals

🏥 Healthcare

Biotechnology • Pharmaceuticals • Healthcare

Thermo Fisher Scientific is the world leader in serving science, with a stated mission to enable customers to make the world healthier, cleaner and safer. The company provides a broad portfolio of laboratory instruments, analytical technologies, diagnostics, consumables, software and services that support life‑sciences research, analytical testing, clinical diagnostics and the development and manufacture of therapies. Its operations and offerings (as described on its site and in its news) include advanced imaging and electron microscopes, chromatography and mass‑spectrometry systems, genetic and clinical testing, lab automation and AI tools, bioprocessing and contract development/manufacturing services (brands cited include Thermo Scientific, Applied Biosystems, Invitrogen, Gibco, Fisher Scientific, Unity Lab Services, Patheon and PPD). Thermo Fisher reports annual revenue over $45 billion and emphasizes corporate social responsibility, environmental and community programs alongside its scientific products and services.

📋 Description

• Provide medical oversight of clinical trials to ensure company SOPs, client directives, good clinical practice, and regulatory requirements are followed • Attend and present at investigator and sponsor meetings • Provide medical consultation to clients, investigators, and project team members • Support business development activities • Provide medical review and analysis for clinical-trial serious adverse events, marketed-product ICSRs, periodic safety reports, and other client deliverables • Ensure Pharmacovigilance-delegated tasks are properly executed and comply with regulations, ICH guidelines, client directives, and company SOPs/WPDs • Answer study-related medical questions and maintain communication with associates and clients • Provide therapeutic and protocol training on assigned studies • Assist with writing and/or reviewing CSRs, IND/NDA reports, ICSRs, signal detection reports, periodic reports, RMPs, REMS, and CTD modules • Monitor clinical-trial safety variables, including adverse events, laboratory abnormalities, patient medical-status changes, concomitant medications, and unblinding requests • Discuss medical concerns with principal investigators and clients and make clinical judgments regarding investigational studies • Review adverse events of special interest, serious adverse events, and clinical outcome events • Perform contracted data review and validate safety data, coding listings, and potential safety concerns • Manage signal-detection activities and review aggregate reports • Contribute to label updates, dossier maintenance, and risk-management activities • Medically review adverse-event and serious-adverse-event data from solicited, spontaneous, and literature sources

🎯 Requirements

• MD or equivalent required • Active medical licensure preferred • At least one of: clinical experience treating patients in the relevant specialty/sub-specialty comparable to 2 years; suitable clinical trial experience in a CRO, pharmaceutical company, or as a principal investigator comparable to 1–2 years; direct safety/Pharmacovigilance experience comparable to 2 years • For Senior Medical Director: clinical experience comparable to 2 years plus suitable clinical trial experience comparable to 1–2 years or direct safety/Pharmacovigilance experience comparable to 2 years • Therapeutic expertise across one or more medical specialties or sub-specialties • Strong decision-making, problem-solving, organizational, and analytical skills • Excellent oral and written communication skills • Working knowledge of relevant safety databases, such as MedDRA • Ability to travel domestically and internationally • Ability to work independently, analyze work with attention to detail, and process and prioritize sensitive complex information • Proficiency in basic computer applications • Fluent spoken and written English • Excellent interpersonal, influencing, and team-building skills • Understanding of FDA, ICH, EMA, and GCP guidelines • Working knowledge of biostatistics, data management, and clinical operations procedures • Ability to mentor/train other staff within Pharmacovigilance • In some cases, an equivalency combining appropriate education, training, and/or directly related experience may be considered

🏖️ Benefits

• Fully remote work mode • Standard Monday–Friday work schedule • Career goals and professional development resources • Mentoring/training opportunities • Global and international work exposure • Occasional domestic and international travel

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