Want more jobs like this?Getjobsthat areRemotedelivered to your inbox every week.

Want more jobs like this?

Getjobsthat areRemotedelivered to your inbox every week.

Get Jobs

Key Responsibilities:Conduct detailed reviews of scientific, medical, and promotional documents to ensure consistency, scientific validity, and compliance with regulations and guidelines.Collaborate with regulatory and legal teams to ensure compliance with applicable requirements and international standards for diagnostics, including oncology.Apply medical or related field expertise to evaluate clinical data, research findings, and diagnostic information, ensuring scientific accuracy and relevance in oncology and pathology.Contract Management: Supervise the management of contracts, including reviewing, negotiating, and ensuring compliance with requirements.Quality Assurance: Participate in quality assurance activities, including reviewing protocols, clinical study reports, scientific papers, and contracts for accuracy and adherence to regulatory guidelines.Cross-Functional Teamwork: Collaborate with all internal partners to ensure scientific, regulatory, and contractual alignment.Process Improvement: Identify areas for improvement in the review and contracting process, developing and implementing strategies to increase efficiency while maintaining quality standards.Minimum Requirements/Qualifications:Bachelor’s or advanced degree in a health-related field such as Oncology, Molecular Biology, Biochemistry, or a closely related field.Minimum of 3 years of experience in medical/scientific review, regulatory compliance, and contract management within the diagnostics or pharmaceutical industry.In-depth knowledge of oncology diagnostics and related scientific principles.Familiarity with global regulatory requirements (FDA, EMA, etc.).Experience in contract review and management within a scientific or medical setting.Proficiency in medical writing and document management systems is a plus.Familiarity with software tools for document submission and review, as well as contract management software.Excellent attention to detail and ability to handle complex scientific data.Ability to work collaboratively in a fast-paced, multidisciplinary environment.Join our team and be part of a company that values diverse experiences, backgrounds, and perspectives. Thermo Fisher Scientific is an equal opportunity employer and offers reasonable accommodations for individuals with disabilities during the application process.