Director, Safety Assessment & GLP Strategy

120 Altasciences Preclinical Seattle LLC; Seattle (WA); On-site; USD 126,000 - 200,000; Full time

Benefits offered by this job

Health/Dental/Vision Insurance Plans

401(k)/RRSP with Employer Match

Paid Vacation and Holidays

Paid Sick and Bereavement Leave

Employee Assistance & Telehealth

Training & Development Programs

Employee Referral Bonus

Job summary

Altasciences Preclinical Seattle LLC is seeking a senior leader to direct the Safety Assessment department, ensuring GLP compliance, strategic planning, and efficient operations. You will mentor staff, coordinate with Study Directors, and engage with clients and regulators to meet study objectives and quality standards.

The role requires advanced degrees in biomedical fields, extensive preclinical safety experience, and strong communication skills for regulatory submissions and client

Qualifications

• Ph.D. in biomedical field or MD/DVM; master’s with relevant training may apply.
• Minimum seven years evaluating preclinical safety and toxicology in pharma/biotech, CROs, or similar.
• Experience leading groups or teams in a regulated environment.
• Experience writing and presenting preclinical safety reports for regulatory submissions.
• GLP training and knowledge of regulatory guidelines for preclinical drug development.

Responsibilities

• Direct GLP compliance initiatives and oversee department policies and SOPs.
• Lead strategic planning and resource management for Safety Assessment programs.
• Mentor staff on drug development, client management, and study design.
• Engage with regulatory agencies and support business development activities.

Skills

Leadership

GLP compliance

Regulatory communications

Scientific writing

Education

Ph.D. in relevant biomedical field

MD

DVM

Masters degree with appropriate training

Job description

Altasciences Preclinical Seattle LLC is seeking a senior leader to direct the Safety Assessment department, ensuring GLP compliance, strategic planning, and efficient operations. You will mentor staff, coordinate with Study Directors, and engage with clients and regulators to meet study objectives and quality standards.

The role requires advanced degrees in biomedical fields, extensive preclinical safety experience, and strong communication skills for regulatory submissions and client