Remote Pharmaceuticals Jobs • Regulatory Submissions

The Staff Toxicologist will play a critical role in authoring and guiding toxicological risk assessments for medical devices and combination products. This position involves performing high-level biological safety evaluations, providing strategic input on regulatory submissions, and mentoring junior staff members as needed. The Staff Toxicologist will ensure the safety and compliance of products.

As the primary sponsor liaison and advocate, the Clinical Project Manager will plan, execute, manage and monitor regional, single modality or therapeutic area clinical research projects. The candidate will manage the day to day activities and performance of a multidisciplinary project team, ensuring all decisions align with corporate, industry, sponsor and regulatory requirements.

As a pivotal member of the Nonclinical Safety team, the Senior Scientist, Study Toxicologist, collaborates with project toxicologists and manages the outsourcing, design, and oversight of safety pharmacology and toxicology studies at contract research organizations (CROs). This position requires a strategic and detail-oriented professional who can effectively coordinate studies and ensure high-quality data.