**Work Schedule**
Standard (Mon-Fri)
**Environmental Conditions**
Office
Key Responsibilities:
- Document Review Management: Conduct detailed reviews of scientific, medical, and promotional documents. Ensure consistency, scientific accuracy, and compliance with regulations and guidelines.
- Regulatory/Legal Compliance: Act as the point of contact for regulatory and legal teams. Ensure all documents and processes meet requirements (e.g., Sunshine Act, MedTech Code) and comply with diagnostic standards, especially in oncology.
- Contract Management: Manage contracts by reviewing, negotiating, and ensuring legal and regulatory compliance. Collaborate with internal teams to ensure timely and accurate contract execution related to research, clinical studies, and partnerships.
- Quality Assurance: Participate in quality assurance activities. Review protocols, clinical study reports, scientific papers, and contracts for accuracy and adherence to regulatory guidelines.
- Process Improvement: Identify areas for improvement in the review process. Develop and implement strategies to boost efficiency while maintaining high-quality standards.
Minimum Requirements/Qualifications:
- Bachelor's or advanced degree in Oncology, Molecular Biology, Biochemistry, or a closely related field.
- Experience in medical/scientific review, integral regulatory compliance, and contract management within diagnostics or pharmaceuticals.
- Strong knowledge of oncology diagnostics and related scientific principles.
- Proficiency in contract review and management in a scientific or medical setting.
- Ability to thrive in a fast-paced, multidisciplinary environment, with excellent attention to detail.