Study Director for pilot and IND-enabling studies. Experience in chronic, investigative and carcinogenicity study designs. Responsible for the planning, conduct and successful reporting of assigned studies. Participate in report review and generation process. Develop new capabilities for Ricerca Biosciences. Communicate with Sponsors as required.
ESSENTIAL DUTIES AND RESPONSIBILITIES:
Participate in the proposal and bid development process
Serve as a key contact for sponsors
Participate in and coordinate all phases of the study planning process with Client Services and technical and laboratory support operations
Responsible for study design and generation of protocols
Interpret study data, write reports and draw conclusions
Develop and foster business relationships
Perform other duties as assigned
PhD in Toxicology or Pharmacology or a related field. Ability to interact with multiple personality types and cultural backgrounds.
Working knowledge of Good Laboratory Practices regulations
Attention to detail and excellent interpersonal and communication skills
We offer a competitive wage along with a comprehensive benefit plan.
Ricerca is an equal opportunity employer.