Study Director

2 months ago

sacramento, United States RPM ReSearch Full time

Join Our Team as a Study Director and Research Scientist

Your New Opportunity: We're all about teamwork. Every role contributes to the discovery, development, and manufacturing of new drug therapies, helping us get them to the people who need them faster. By living our values—Employee Development, Customer Focus, Quality and Excellence, Respect, and Integrity—we create a passionate, collaborative work environment. Whether you’re a recent graduate or seeking your next career move, your future could be with us.


Why Join Us?

  • Impactful Work: Play a significant role in global health and well-being.
  • Collaborative Environment: Work with a team that values your input and expertise.
  • Growth Opportunities: Whether you’re just starting your career or looking to advance, we offer a dynamic environment to grow and thrive.


The Role: Study Director, Research Scientist Are you passionate about preclinical research? As a Study Director, you’ll be the single point of control for assigned studies, responsible for the interpretation, analysis, documentation, and reporting of study results for both GLP and non-GLP studies.


What You’ll Do:

  • Oversee the technical conduct of studies and manage the 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.


What You Need to Succeed:

  • Education: Master’s or Doctoral Degree in a relevant scientific discipline (or equivalent experience).
  • Experience: 3+ years as a Study Director for in vivo studies in a biopharmaceutical company or CRO. Experience in Toxicology is a plus.
  • Skills: Intermediate to Advanced Computer Skills, strong planning and organizational skills, ability to manage change, and effective communication of scientific data.
  • Other: Must complete Study Director Training and maintain ongoing scientific and professional education.

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