Global Lead Pharmacologist & Toxicologist

Attaineo Search, Inc.; United States; Remote; USD 150,000 - 190,000; Full time

Job summary

Attaineo seeks a Lead Pharmacologist/Toxicologist to lead pharmacology and toxicology across developmental programs for complex drug products. The role involves designing regulatory studies, constructing analyses and positional papers (IND/NDA) and guiding external testing facilities.

Responsibilities include supervising scientists, ensuring data quality, and interfacing with regulatory authorities to defend development programs. Strong communication and regulatory expertise are essential.

Qualifications

• Earned doctoral degree in Toxicology, Pharmacology or related field with 5+ years of post-baccalaureate experience (or master's with 8+ years, or bachelor's with 10+ years).
• Knowledge of GLP and ISO regulations and world health authority guidelines is essential.
• Experience in regulatory study documentation (IND/NDA, etc.) and cross-functional collaboration.

Responsibilities

• Lead Global Pharmacology and Toxicology programs for developmental drug products.
• Develop and defend regulatory study documents and technical analyses.
• Oversee selection and oversight of contract testing facilities for nonclinical studies.
• Review SOPs and supervise junior scientists as needed.
• Represent the department in meetings with regulatory authorities and internal stakeholders.
• Communicate performance expectations clearly and work across teams.

Skills

Oral and written communication

Organizational skills

Computer skills

Team collaboration

Independent judgment

Regulatory awareness

Education

Doctoral degree in Toxicology or Pharmacology or related field

Master's degree in Toxicology/Pharmacology or related field

Bachelor's degree in a related field

Job description

Attaineo seeks a Lead Pharmacologist/Toxicologist to lead pharmacology and toxicology across developmental programs for complex drug products. The role involves designing regulatory studies, constructing analyses and positional papers (IND/NDA) and guiding external testing facilities.

Responsibilities include supervising scientists, ensuring data quality, and interfacing with regulatory authorities to defend development programs. Strong communication and regulatory expertise are essential.