Senior Medical Researcher

Role & responsibilities

• Perform comprehensive scientific reviews, including the mechanics of how medicines work and their delivery methods.
• Conduct technical analyses of last study results, focusing on key metrics such as efficacy and bioavailability.
• Analyze and evaluate the next phases of clinical trials to inform strategic decisions.
• Review scientific literature to support project initiatives and ensure alignment with current research trends.
• Prepare and review comprehensive reports for submission to the US FDA, including New Drug Applications (NDAs) and Biologics License Applications (BLAs).
• Oversee the development and quality assurance of documents pertaining to FDA protocols, patient safety, and clinical trial data.
• Design and produce effective training modules tailored for healthcare professionals, sales teams, and insurance agencies.
• Acquire and maintain in-depth knowledge of global drug discovery and medical device research, identifying strategic investment and collaboration opportunities.
• Conduct thorough competitive analyses to inform strategic decision-making.
• Review and analyze patent documents submitted by companies and academic research groups, contributing to informed strategic planning.

Preferred candidate profile

• In-depth knowledge of FDA regulations and submission processes.
• Exceptional writing, editing, and communication skills with a keen eye for detail.
• Proven ability to manage multiple projects simultaneously while meeting deadlines

Perks and benefits

Health Insurance

Paid Time-Off