Medical Director, Nephrology & Internal Medicine - Trials

ThermoFisher Scientific; España; Remote; EUR 120,000 - 180,000; Full time

Job summary

Thermo Fisher Scientific in Spain is seeking a Medical Director to provide medical leadership for clinical trials and safety evaluation within our client environment. You will oversee study teams, ensure patient safety, review protocols, CSRs and regulatory documents, and collaborate with global medical indications and internal departments to address issues and optimize trial conduct.

You will lead medical monitoring, liaise with investigators and regulators, and train site staff while ensuring

Qualifications

• MD with clinical trials experience in pharma industry.
• Experience with NDA submissions and regulatory guidelines.
• Fluent in English, both spoken and written.
• Strong communication and presentation skills; team player.

Responsibilities

• Provide medical leadership to study teams and contribute to protocol development, CSR, ICFs and other key documents.
• Real-time medical monitoring to ensure patient safety and validity of study endpoints.
• Serve as liaison between sponsor and internal departments across all study phases; educate sites.
• Medical training of site staff and investigators; respond to queries and regulatory questions.
• Ensure SOP and GCP compliance; collaborate with cross-functional teams to manage risks and issues.

Skills

Medical leadership

Regulatory knowledge

Clinical communication

English fluency

Team collaboration

Education

Medical Doctor (MD)

Specialty in Nephrology or Internal Medicine

Job description

Thermo Fisher Scientific in Spain is seeking a Medical Director to provide medical leadership for clinical trials and safety evaluation within our client environment. You will oversee study teams, ensure patient safety, review protocols, CSRs and regulatory documents, and collaborate with global medical indications and internal departments to address issues and optimize trial conduct.

You will lead medical monitoring, liaise with investigators and regulators, and train site staff while ensuring