Senior Scientist, CellularMolecular Biology II

North Chicago, IL - USA

Monthly Salary: Not Disclosed

Posted on: Yesterday

Vacancies: 1 Vacancy

Job Summary

Role Summary

Generate and execute novel scientific research or development that impacts safety evaluation for programs across therapeutic areas within preclinical safety. Design 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 advances and integrate this knowledge to drive scientific progress for programs.

Responsibilities

Conduct routine and exploratory molecular pathology endpoints on tissues cells and other matrices (such as organ-on-chip) including but not limited to IHC ISH laser-capture microdissection off-target binding assessments immunofluorescence (including multiplexing) and electron microscopy.
Support development and deployment of digital pathology tools to support rapid pathologic evaluation of exploratory studies.
Demonstrate the ability to identify and resolve key project hurdles and assumptions by effectively utilizing available information and technical expertise.
Proactively seek out new information in the literature and incorporate this into individual project(s) as well as the overall safety assessment strategy.
Seize opportunities to pursue project-relevant methods and techniques that are in line with the groups strategy.
Maintain a high level of productivity in the lab.
May mentor/supervise a team of one or more and evaluate the performance of those individuals; is accountable for the effective performance of the team/individuals.
Understand and adhere to corporate standards regarding code of conduct safety appropriate handling of materials controlled drug and radioactive compounds and animal care where applicable.
Collaborate effectively with other teams to identify areas of scientific advancement and efficiency.

Qualifications :

Qualifications

Bachelors Degree or equivalent education and typically 12 years of experience Masters Degree or equivalent education and typically 10 years of experience PhD and typically 4 years of experience.
Possess thorough theoretical and practical understanding of own scientific discipline.
Effective writer and communicator of research.
People leadership and management experience preferred.

Additional Information :

Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:

The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location and we may ultimately pay more or less than the posted range. This range may be modified in the future.
We offer a comprehensive package of benefits including paid time off (vacation holidays sick) medical/dental/vision insurance and 401(k) to eligible employees.
This job is eligible to participate in our short-term incentive programs.
This job is eligible to participate in our long-term incentive programs

Note: No amount of pay is considered to be wages or compensation until such amount is earned vested and determinable. The amount and availability of any bonus commission incentive benefits or any other form of compensation and benefits that are allocable to a particular employee remains in the Companys sole and absolute discretion unless and until paid and may be modified at the Companys sole and absolute discretion consistent with applicable law.

AbbVie is an equal opportunity employer and is committed to operating with integrity driving innovation transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.

US & Puerto Rico only - to learn more visit & Puerto Rico applicants seeking a reasonable accommodation click here to learn more:

Work :

Employment Type :

Full-time

Role SummaryGenerate and execute novel scientific research or development that impacts safety evaluation for programs across therapeutic areas within preclinical safety. Design new scientific proposals and lead those efforts. Investigate identify develop and optimize new methods and techniques. Act ...

Role Summary

Responsibilities

Conduct routine and exploratory molecular pathology endpoints on tissues cells and other matrices (such as organ-on-chip) including but not limited to IHC ISH laser-capture microdissection off-target binding assessments immunofluorescence (including multiplexing) and electron microscopy.
Support development and deployment of digital pathology tools to support rapid pathologic evaluation of exploratory studies.
Demonstrate the ability to identify and resolve key project hurdles and assumptions by effectively utilizing available information and technical expertise.
Proactively seek out new information in the literature and incorporate this into individual project(s) as well as the overall safety assessment strategy.
Seize opportunities to pursue project-relevant methods and techniques that are in line with the groups strategy.
Maintain a high level of productivity in the lab.
May mentor/supervise a team of one or more and evaluate the performance of those individuals; is accountable for the effective performance of the team/individuals.
Understand and adhere to corporate standards regarding code of conduct safety appropriate handling of materials controlled drug and radioactive compounds and animal care where applicable.
Collaborate effectively with other teams to identify areas of scientific advancement and efficiency.

Qualifications :

Qualifications

Bachelors Degree or equivalent education and typically 12 years of experience Masters Degree or equivalent education and typically 10 years of experience PhD and typically 4 years of experience.
Possess thorough theoretical and practical understanding of own scientific discipline.
Effective writer and communicator of research.
People leadership and management experience preferred.

Additional Information :

Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:

The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location and we may ultimately pay more or less than the posted range. This range may be modified in the future.
We offer a comprehensive package of benefits including paid time off (vacation holidays sick) medical/dental/vision insurance and 401(k) to eligible employees.
This job is eligible to participate in our short-term incentive programs.
This job is eligible to participate in our long-term incentive programs

AbbVie is an equal opportunity employer and is committed to operating with integrity driving innovation transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.

US & Puerto Rico only - to learn more visit & Puerto Rico applicants seeking a reasonable accommodation click here to learn more:

Work :

Employment Type :

Full-time

Key Skills

Laboratory Experience
Mammalian Cell Culture
Biochemistry
Assays
Protein Purification
Research Experience
Next Generation Sequencing
Research & Development
cGMP
Cell Culture
Molecular Biology
Flow Cytometry

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About Company

AbbVie

AbbVie is a global biopharmaceutical company focused on creating medicines and solutions that put impact first for patients, communities, and our world. We aim to address complex health issues and enhance people's lives through our core therapeutic areas: immunology, oncology, neuro ... View more

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