Senior Scientist, II
AbbVie
5 hours ago
Remote friendly (North Chicago, IL)
United States
Clinical Research and Development
Purpose
Conceive and execute novel scientific research or development that achieves projects and area goals. Generate new scientific proposals and lead those efforts. Investigate, identify, develop, and optimize new methods and techniques. Act as a lead scientist in his/her area of expertise and critically evaluate relevant scientific and regulatory advances and integrate this knowledge into research or development programs.
Responsibilities
- Demonstrate the ability to resolve key project hurdles and assumptions by effectively utilizing available information and technical expertise.
- Publish research in peer-reviewed journals and present work at scientific conferences.
- Proactively seek out new information in the literature and incorporate this into individual project(s) and the overall program.
- Pursue project-relevant leads in line with the group’s strategy.
- Maintain a high level of productivity in the lab.
- Understand and adhere to corporate standards regarding code of conduct, safety, appropriate handling of materials, controlled drug and radioactive compounds, GxP compliance, and animal care where applicable.
- May mentor/supervise a team of one or more and guide and evaluate performance; accountable for effective performance of the team/individuals.
Qualifications
- Bachelor’s degree (typically 12 years’ experience), Master’s degree (typically 10 years’ experience), or PhD (typically 4 years’ experience).
- Thorough theoretical and practical understanding of own scientific discipline.
- Effective writer and communicator of research or other regulatory materials.
Benefits
- Paid time off (vacation, holidays, sick), medical/dental/vision insurance, and 401(k) to eligible employees.
- Eligible to participate in long-term incentive programs.
Conceive and execute novel scientific research or development that achieves projects and area goals. Generate new scientific proposals and lead those efforts. Investigate, identify, develop, and optimize new methods and techniques. Act as a lead scientist in his/her area of expertise and critically evaluate relevant scientific and regulatory advances and integrate this knowledge into research or development programs.
Responsibilities
- Demonstrate the ability to resolve key project hurdles and assumptions by effectively utilizing available information and technical expertise.
- Publish research in peer-reviewed journals and present work at scientific conferences.
- Proactively seek out new information in the literature and incorporate this into individual project(s) and the overall program.
- Pursue project-relevant leads in line with the group’s strategy.
- Maintain a high level of productivity in the lab.
- Understand and adhere to corporate standards regarding code of conduct, safety, appropriate handling of materials, controlled drug and radioactive compounds, GxP compliance, and animal care where applicable.
- May mentor/supervise a team of one or more and guide and evaluate performance; accountable for effective performance of the team/individuals.
Qualifications
- Bachelor’s degree (typically 12 years’ experience), Master’s degree (typically 10 years’ experience), or PhD (typically 4 years’ experience).
- Thorough theoretical and practical understanding of own scientific discipline.
- Effective writer and communicator of research or other regulatory materials.
Benefits
- Paid time off (vacation, holidays, sick), medical/dental/vision insurance, and 401(k) to eligible employees.
- Eligible to participate in long-term incentive programs.