
Medical Director
Posted 2 hours ago

Posted 2 hours ago
This is a fully remote position, open to applicants in Brazil.
• Oversees the medical aspects of clinical trials
• Ensures compliance with SOPs, client instructions, and regulatory standards
• Participates in and presents at meetings with investigators and sponsors
• Offers medical advice to clients and investigators
• Monitors all safety aspects of clinical studies
• Manages signal detection processes and evaluates aggregate reports
• Assists in the writing and/or review of various reports and documents
• MD degree required with a focus in Oncology or Hemato-Oncology
• Clinical experience in patient treatment (equivalent to 2 years)
• Relevant clinical trial experience in a CRO, pharmaceutical company, or as a principal investigator (equivalent to 1-2 years)
• Direct experience in safety/Pharmacovigilance (equivalent to 2 years)
• Familiarity with FDA, ICH, EMA, and GCP guidelines
• Willingness to travel domestically and internationally
• Proficient in both spoken and written English
• Health insurance
• Competitive salary
• Professional development opportunities
• Flexible working hours
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