How to Apply:

Please email your resume and cover letter to careers@oneworldhealth.org or mail to:

Institute for OneWorld Health
c/o Human Resources
50 California Street, Suite 500
San Francisco, CA 94111

Due to the volume of inquiries, we are unable to respond to phone calls. We will acknowledge receipt of your resume via email, and will contact you if you are a potential candidate for the position.

Thank you for your interest in OneWorld Health.

OneWorld Health is proud to be an equal opportunity employer committed to providing a diverse workplace.


  

Employment

Department: Research and Development

Job Title: Senior Toxicologist

Job Location: San Francisco, CA

Description:

Reports To: Vice President, Research and Preclinical Development
Status: Part-time, Exempt

POSITION SUMMARY
 
The Sr. Toxicologist will be responsible for the safety of evaluation of drug development candidates in support of portfolio development, early clinical ADME trial, IND and NDA filings. S/he develops, implements, and monitors project-specific protocols for preclinical studies related to general toxicology and safety pharmacology. The Sr. Toxicologist will provide expert advice to project teams, executives, and will interface with regulatory agencies on matter related to his/her areas of expertise. Specific responsibilities related to preclinical development include designing, scheduling, and resourcing safety studies; reporting and reviewing data; and preparing and reviewing preclinical study reports and relevant sections for U.S. and international regulatory submissions. 

Job Requirements:

ESSENTIAL DUTIES AND RESPONSIBILITIES include the following; other duties may be assigned. 
 
  • Develops, implements, and oversees protocols, timelines, and budgets for preclinical studies
  • Oversees and participates in the critical analysis of preclinical study results and reports
  • Prepares and presents study summaries for internal discussions and regulatory submissions
  • Participates as a member of project teams to provide expert advice
  • Domestic and/or international travel related to professional responsibilities may account for approximately ten percent of the annual work time.
 
ESSENTIAL QUALIFICATIONS
 
  • Ph.D. in related pharmaceutical sciences, Pharmacology or Toxicology. American Board of Toxicology certified preferred
  • Minimum of 5 -8 years experience in drug development, specifically preclinical study research and operations, safety evaluation and reporting, and regulatory submissions pertaining to infectious diseases
  • Expert knowledge of regulations pertaining to GLP, and ICH, and demonstrated experience in designing experiments, supervising CROs to implement preclinical studies protocol
  • Effective leadership skills and proven ability to foster team productivity and cohesiveness
  • Excellent communication skills and the innate flexibility to work in a rapidly growing organization

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