What are the responsibilities and job description for the Research Scientist / Study Director position at RPM ReSearch?
Study Director - Research Scientist
Your New Company!
At our CRO, we move in unison to assist and contribute to the discovery, development, and manufacturing of new drug therapies to bring them faster to the people who need them. Regardless of your role, you will play an essential part in impacting health and well-being globally. By fostering our core values—Employee Development, Customer Focus, Quality and Excellence, Respect, and Integrity—we create a passionate and collaborative work environment.
If you’re a recent graduate or a seasoned professional seeking your next career opportunity, it’s time to discover your future with us.
About the Role
As a Study Director, Research Scientist, your passion for preclinical research will shine as you act as the single point of control for assigned GLP and non-GLP studies. You’ll ensure the interpretation, analysis, documentation, and reporting of study results are accurate and impactful.
Key Responsibilities
Oversee the technical conduct of studies and represent the single point of study control.
Interpret, analyze, document, and report study results in compliance with GLPs and other applicable regulations.
Consult with Sponsors and internal teams during protocol development to meet study objectives.
Respond to client inquiries and actively participate in discussions regarding studies.
Coordinate schedules, logistics, and milestones across internal departments and external collaborators.
Ensure study personnel are adequately trained and educated for their roles.
Monitor, track, and communicate study progress while addressing unforeseen circumstances.
Analyze study data and prepare comprehensive reports.
Review, revise, and write SOPs as needed.
Qualifications
Master’s or Doctoral degree in a relevant scientific discipline; equivalent experience may substitute educational requirements.
3 years of experience as a Study Director for in vivo studies (GLP experience required).
Background in toxicology is a plus.
Strong data analysis and interpretation skills, including the use of appropriate mathematical and statistical methods.
Excellent planning, organizational, and communication skills.
Proven ability to work effectively in a team and under time constraints.
Demonstrated attention to detail and commitment to accuracy.
Why Join Us?
We offer competitive compensation within the range of $74,000 to $110,000 per year, based on experience, skills, education, and other factors. Join a team where your contributions make a real difference in advancing drug development and improving global health.
Apply today and help shape the future of drug development!
Salary : $74,000 - $110,000
