Senior Toxicology Study Director | GLP/GCP Expert

BAS EVANSVILLE INC; Evansville (IN); On-site; USD 70,000 - 90,000; Full time

Benefits offered by this job

Health and dental coverage

Short‑ and long‑term disability

Paid time off

Paid parental leave

401(k)

More benefits as applicable

Job summary

BAS EVANSVILLE INC is seeking a Study Director to oversee protocol development, study coordination, and regulatory reporting. The role requires a Bachelor's degree and significant experience in laboratory settings.

Key responsibilities include managing study protocols, ensuring compliance with GLP regulations, and preparing reports. Candidates must possess strong organizational skills, knowledge of FDA guidelines, and a background in biological sciences.

Benefits include health coverage, paid time off, and a 401(k) plan.

Qualifications

• Bachelor’s degree and 10 years of relevant experience, or Master’s degree and 5 years of relevant experience.
• Knowledge of cGMP, GLP, GCP, and OECD regulations is required.
• Ability to document analytical results.

Responsibilities

• Responsible for all phases of protocol development and study coordination.
• Monitor study progress and report results to the sponsor.
• Maintain knowledge of FDA and other regulatory guidelines.

Skills

Good organizational skills

Ability to use a computer to compile and maintain databases

Knowledge of cGMP/GLP/GCP regulations

Good written and oral communication skills

Ability to work independently

Education

Bachelor's degree with 10 years of relevant experience

Master's degree with 5 years of relevant experience

Doctoral degree with at least 2 years of laboratory animal experience

Tools

Windows-based software applications (Excel, Word, PowerPoint)

Job description

BAS EVANSVILLE INC is seeking a Study Director to oversee protocol development, study coordination, and regulatory reporting. The role requires a Bachelor's degree and significant experience in laboratory settings.

Key responsibilities include managing study protocols, ensuring compliance with GLP regulations, and preparing reports. Candidates must possess strong organizational skills, knowledge of FDA guidelines, and a background in biological sciences.

Benefits include health coverage, paid time off, and a 401(k) plan.