On-site Study Supervisor: GLP Animal Research

Altasciences; Everett, Northern (WA, KY); Hybrid; USD 43,000 - 48,000; Full time

Benefits offered by this job

Health insurance

401(k)/RRSP with Employer Match

Paid Vacation and Holidays

Free employee parking

Free lunch

Job summary

Altasciences in Everett, Washington is seeking a Study Supervisor to oversee studies, procedures, and research assignments on site. You will coordinate study teams, ensure trained staff, necessary supplies, and data collection processes are in place.

The role requires a Bachelor’s degree with at least 2 years of related experience; LATG preferred. You’ll monitor GLP compliance, document procedures, and collaborate with study directors to meet timelines.

Qualifications

• Bachelor’s degree and at least 2 years of related experience.
• LATG certification preferred.
• Ability to read and interpret technical documents and manuals.
• Ability to write advanced reports and correspondence.
• Excellent verbal and written communication skills.
• Strong interpersonal skills.
• Ability to manage multiple priorities.
• Self-directed and proactive.
• Industry experience is a plus.

Responsibilities

• Supervise studies, procedures, and research assignments.
• Coordinate duties of personnel and study teams.
• Assist with sample and data collection for studies.
• Ensure trained staff and required supplies for data collection.
• Record data and ensure GLP compliance.

Skills

LATG certification

Technical reading

Technical writing

Verbal communication

Interpersonal skills

Prioritization

Self-direction

Education

Bachelor’s degree

Job description

Altasciences in Everett, Washington is seeking a Study Supervisor to oversee studies, procedures, and research assignments on site. You will coordinate study teams, ensure trained staff, necessary supplies, and data collection processes are in place.

The role requires a Bachelor’s degree with at least 2 years of related experience; LATG preferred. You’ll monitor GLP compliance, document procedures, and collaborate with study directors to meet timelines.