Senior Medical Director, Trial Physician – Neurology

🔥 1 hour ago

🇦🇷 Argentina – Remote

⏰ Full Time

🟠 Senior

👨‍⚕️ Medical Director

👻 Ghost score 10%

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Logo of Thermo Fisher Scientific

Thermo Fisher Scientific

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 clear medical leadership to study teams and ensure reliable, high-quality study data within time and budget • Create clinical trial protocols using the latest scientific information • Contribute to site selection and review and approval of study protocols, amendments, CSRs, ICFs, CRFs, protocol deviation decisions, and other clinical documents • Conduct real-time medical monitoring of clinical studies • Ensure medical validity of primary endpoints and study-subject safety • Identify, escalate, and correct medical issues in consultation with the Global Medical Indication Lead • Interpret clinical trial data for regulatory documents, manuscripts, and other publications • Serve as the 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 executive and independent safety committees when applicable • Provide medical training to site staff at investigator meetings and CRA training for new indications • Ensure medical compliance by understanding and applying relevant SOPs and GCP • Collaborate with cross-functional study team members to clarify medical risks, issues, and results • Work with a global, client-dedicated biotech organization developing autoimmune disease treatments • Travel occasionally to domestic and international site locations

🎯 Requirements

• Medical Doctor or equivalent degree required • Board certification(s) preferred • Specialty education, such as residency/fellowship, required in neurology • Patient treatment and/or research experience • 1–3 years of industry experience required in clinical development within a Pharmaceutical, Biotech, or CRO organization • Neuromuscular disease expertise highly preferred • Excellent written and spoken English • Ability to travel • Understanding and experience with NDA submission process • Understanding of regulatory guidelines for adverse event reporting • Interpersonal skills to lead a study team and exercise judgment on issues requiring immediate escalation • Proactive problem-solving and negotiation skills • Strong communication and collaboration skills in a cross-functional, matrixed organization • Must be legally authorized to work in North America without sponsorship • Must be able to pass a comprehensive background check, including drug screening where applicable • Must be located in the EST time zone • Ability to access and use in-house and commercial computer software • Regular and consistent attendance • Ability to work independently, multitask, perform under stress, and sustain intense concentration • Ability to perform the stated physical activities, including occasional lifting and carrying of 15–20 lbs.

🏖️ Benefits

• Annual incentive plan bonus • Healthcare • Range of employee benefits • Career and development prospects • Fully remote work arrangement • 10–20% travel range, including possible international travel

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