Senior Preclinical Research Scientist
2 weeks ago
Role Overview:
RPM ReSearch seeks a highly skilled Senior Preclinical Research Scientist to direct the technical conduct of studies and manage the interpretation, analysis, and reporting of results. As a Study Director, you will oversee GLP and non-GLP studies, collaborate with sponsors and internal departments, and ensure accurate recording and verification of all experimental data.
Key Responsibilities:
- Oversee the technical conduct of studies, manage interpretation, analysis, and reporting of results.
- Perform duties following GLPs and other relevant regulations.
- Collaborate with sponsors, study directors, and others to optimize protocol design.
- Coordinate study schedules and logistics with clients, subcontractors, and internal departments.
- Ensure study personnel are properly trained and educated for their roles.
- Monitor study milestones and ensure accurate recording and verification of all experimental data.
- Communicate ongoing study activities and results to sponsors.
- Analyze and interpret study data, preparing comprehensive study reports.
- Maintain documentation, protocols, and study reports, ensuring all are archived appropriately.
- Review, revise, and write SOPs as necessary.
Requirements:
- Master's or Doctoral Degree in a relevant scientific discipline (or equivalent experience).
- 3+ years as a Study Director for in vivo studies in a biopharmaceutical company or CRO. Experience in Toxicology is a plus.
- Intermediate to Advanced Computer Skills, strong planning and organizational skills, ability to manage change, and effective communication of scientific data.
- Must complete Study Director Training and maintain ongoing scientific and professional education.
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