Medical Director – Clinical Trial Physician, Rheumatology

Job not on LinkedIn

🕒 February 10

🌲 North Carolina – Remote

🌲 North Carolina – Remote

⏰ Full Time

🔴 Lead

👨‍⚕️ Medical Director

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Thermo Fisher Scientific

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1956

🧬 Biotechnology

💊 Pharmaceuticals

🔬 Science

Biotechnology • Pharmaceuticals • Science

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

• Provides clear medical leadership in the Study team • working in close collaboration with the other members of this cross functional team • Provide medical leadership to the study teams, including creating clinical trial protocols • contribute to site selection • review and approval of study protocols and amendments • Clinical Study Reports (CSRs), Informed Consent Forms (ICFs), Case Report Forms (CRFs), protocol deviation decisions • ensure medical validity of each individual primary endpoint as well study subject safety • Ensure study compliance for all medical aspects by understanding and applying all relevant SOPs and GCP • Collaborate with the cross functional study team members

🎯 Requirements

• Medical Doctor or equivalent degree required • Board certification(s) are preferred • Specialty education(e.g. residency/fellowship) required in rheumatology • This should be accompanied by patient treatment and/or research experience • 1-3 years of industry experience preferred • Experience should be in clinical development in a Pharmaceutical, Biotech or CRO organization • Excellent English, both written and spoken is a must • Shown understanding and experience with NDA submission process • Shown understanding of regulatory guidelines for adverse event reporting • Proven interpersonal skills enabling to lead a study team • Pro-active problem solver with negotiation skills • Strong communication skills

🏖️ Benefits

• competitive remuneration • annual incentive plan bonus • healthcare • range of employee benefits