Senior Medical Director – Rheumatology, EMEA

🕒 5 days ago

🇸🇪 Sweden – Remote

⏰ Full Time

🟠 Senior

👨‍⚕️ Medical Director

👻 Ghost score 10%

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Thermo Fisher Scientific

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1956

🏥 Healthcare

📦 Logistics

🏭 Manufacturing

Healthcare • Logistics • Manufacturing

Thermo Fisher Scientific is the world leader in serving science, with annual revenue of more than $40 billion. Their mission is to enable customers to make the world healthier, cleaner, and safer by supporting life sciences research, solving complex analytical challenges, increasing laboratory productivity, and improving patient health through diagnostics and the development of life-changing therapies. With a global team, they offer innovative technologies and pharmaceutical services through brands such as Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon, and PPD.

📋 Description

• Provide medical leadership to clinical study teams • Create clinical trial protocols using current scientific information • Contribute to site selection and review or approve study protocols and amendments, CSRs, ICFs, CRFs, protocol deviation decisions, and other clinical documents • Perform real-time medical monitoring of clinical studies • Ensure medical validity of primary endpoints and study subject safety • Identify medical issues early and proactively address customer concerns with the Global Medical Indication Lead • Consult internal groups on procedural and budgetary items and protocol amendments • Coordinate internal functions to close gaps and resolve issues • Serve as liaison between the sponsor and PPD internal departments throughout study phases • Educate investigator sites on protocol-specific laboratory procedures • Manage day-to-day clinical trial activities and resolve issues or answer queries • Act as medical point of contact for internal and external stakeholders • Interact with investigators and answer IRB and Health Authority questions • Prepare and present materials to study executives and independent safety committees • Provide medical training to site staff and CRA training for new indications • Ensure compliance with medical aspects of studies, SOPs, and GCP • Collaborate with cross-functional study teams to communicate medical risks, issues, and results

🎯 Requirements

• Medical Doctor, with a specialty in Rheumatology • Clinical experience treating patients in hospital • Significant experience within the pharmaceutical industry, clinical trials, and pharmaceutical medicine • Fluency in spoken and written English • Understanding and experience with NDA submission process • Understanding of regulatory guidelines for adverse event reporting • Strong communication and presentation skills • Strong teamwork skills • Ability to understand and apply relevant SOPs and GCP

🏖️ Benefits

• Global career development resources • Work with a global team of 100,000+ colleagues • EEO/Affirmative Action workplace • Meaningful work supporting life-changing therapies and improved health outcomes

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