Reproductive DART Study Supervisor (GLP)

120 Altasciences Preclinical Seattle LLC; Seattle (WA); On-site; USD 39,000 - 50,000; Full time

Benefits offered by this job

Medical Insurance

401(k) with Company Match

Paid Vacation and Holidays

Paid Sick Leave

Training and Development Programs

Career Growth Opportunities

Free Parking

Job summary

Altasciences, a leading CRO, seeks a Study Supervisor for the Developmental & Reproductive Toxicology (DART) team in Seattle. You will support regulated GLP studies, ensure animal welfare, and oversee procedural and data collection tasks across multiple concurrent studies.

The role requires hands-on experience with gestational reproductive toxicology, attention to SOPs, and the ability to work independently in a fast-paced environment.

Qualifications

• High school diploma or equivalent.
• Experience working with laboratory animals in gestational models and reproductive toxicology procedures.
• Ability to perform rat and rabbit handling and procedural techniques safely and effectively.
• Strong attention to detail and ability to follow SOPs.
• Ability to work independently and as part of a multidisciplinary team.

Responsibilities

• Support the execution of regulatory DART studies for rats and rabbits, including fertility, embryo-fetal development, and pre/postnatal studies.
• Observe animals closely and report changes in health, behavior, appetite, activity, or well-being.
• Perform study procedures according to approved protocols, SOPs, and GLP requirements.
• Collect biological samples including blood and urine.
• Administer test materials and treatments using approved routes and techniques.
• Assist with anesthesia, sedation, catheter placement and other procedures according to timelines.
• Assist with reproductive and developmental endpoint collection.
• Perform fetal collection and assessment, tissue and reproductive organ collection and fixation.
• Train staff on technical procedures on animals including injections, blood draws, catheterization, restraining, anesthesia, tissue collection and fetal assessments.
• Monitor progress of studies during In-Life phases to verify adherence to guidelines.
• Create, review, and revise SOPs relating to animals, procedures, and facility issues.
• Document study procedures and results in study notebooks according to GLP regulations.
• Work closely with Study Directors, Veterinary Services, and Operations teams.
• Contribute to continuous improvement initiatives focused on quality and animal welfare.

Skills

Animal handling

GLP compliance

Protocol following

Attention to detail

Independent worker

Team collaboration

Education

High school diploma or equivalent

Experience with gestational models

Tools

SOP compliance

Aseptic technique

Job description

Altasciences, a leading CRO, seeks a Study Supervisor for the Developmental & Reproductive Toxicology (DART) team in Seattle. You will support regulated GLP studies, ensure animal welfare, and oversee procedural and data collection tasks across multiple concurrent studies.

The role requires hands-on experience with gestational reproductive toxicology, attention to SOPs, and the ability to work independently in a fast-paced environment.