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Research Scientist/Study Director

RPM ReSearch
Everett, WA Full Time
POSTED ON 3/18/2025
AVAILABLE BEFORE 4/15/2025

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

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