What are the responsibilities and job description for the Preclinical Operations Manager position at Northern Biomedical Research Inc?
About the Role:
As a Preclinical Operations Manager, you will be responsible for overseeing the planning, execution, and reporting of preclinical studies. You will work closely with cross-functional teams to ensure that all studies are conducted in compliance with regulatory requirements and company standards. Your main objective will be to ensure that preclinical studies are completed on time, within budget, and to the highest quality standards. You will also be responsible for managing and mentoring a team of preclinical operations professionals.
Minimum Qualifications:
- Bachelor's degree in a scientific discipline
- 5 years of experience in preclinical operations or related field
- Experience managing a team of professionals
- Strong knowledge of regulatory requirements for preclinical studies
- Excellent communication and interpersonal skills
Preferred Qualifications:
- Advanced degree in a scientific discipline
- Experience in a pharmaceutical or biotech company
- Experience with GLP and GMP regulations
- Experience with project management software
Responsibilities:
- Oversee the planning, execution, and reporting of preclinical studies
- Ensure that all studies are conducted in compliance with regulatory requirements and company standards
- Manage and mentor a team of preclinical operations professionals
- Collaborate with cross-functional teams to ensure that preclinical studies are completed on time, within budget, and to the highest quality standards
- Identify and mitigate risks associated with preclinical studies
Skills:
As a Preclinical Operations Manager, you will need to have strong leadership, communication, and project management skills. You will also need to have a deep understanding of preclinical study design, execution, and reporting. In addition, you should be able to effectively manage and mentor a team of preclinical operations professionals. Finally, you should be able to identify and mitigate risks associated with preclinical studies, and ensure that all studies are conducted in compliance with regulatory requirements and company standards.
