Pharmacology Director Jobs in Illinois

44 jobs

The Assistant Director, Medical Publishing is responsible for full managerial oversight of multiple product areas for medical publishing activities for Clinical Pharmacology and Pharmametics (CPPM) (ie,scientific abstracts, posters, and manuscripts) and departmental activities and initiatives, as assigned. Key Responsibilities Include: Compliance with applicable Corporate and Divisional Policies...

An Astellas career offers a totally different way to work and live. Astellas is the bright spot in the pharmaceutical industry - not just because of what we do, but in the way we do it. If you are looking for a company where you can change a life, make a dream come true, and light the way for a better tomorrow, Astellas is the place where you can shine. We offer a different kind of work culture. ...

Astellas is the bright spot in the pharmaceutical industry -- not just because of what we do, but in the way we do it. If you are looking for a company where you can change a life, make a dream come true, and light the way for a better tomorrow, Astellas is the place where you can shine. We offer a different kind of work culture. A high standard of ethics is mandatory. Quality is our pledge. Diver...

The Director of Pre-Clinical Development provides expertise and consultation for multiple drug and drug device candidates through all phases of preclinical and clinical development. Serves as a key member of the Pharma R/D Team to ensure that Preclinical Safety strategy is aligned closely with clinical/regulatory/quality development strategy. The Director of Pre-clinical Development facilitat...

Associate Director/Director, Regulatory Affairs, Area and Affiliate - US and Canada As a leading global biopharmaceutical company, AbbVie is committed to addressing the world’s health challenges through the discovery, development and commercialization of advanced therapies and products that have a remarkable impact on people’s lives. As an AbbVie regulatory affairs (RA) professional, you’ll help ...

Associate Director/Director, Regulatory Affairs, Area and Affiliate - US and Canada As a leading global biopharmaceutical company, AbbVie is committed to addressing the world’s health challenges through the discovery, development and commercialization of advanced therapies and products that have a remarkable impact on people’s lives. As an AbbVie regulatory affairs (RA) professional, you’ll help ...

Regulatory Affairs (RA) is the organization within AbbVie that ensures we comply with all regulations and laws pertinent to health care products. The regulatory function is vital to safety and effectiveness of health care products worldwide. Vision: With the patient in mind, be recognized as an Industry Leading Global regulatory affairs organization that designs and delivers optimized global regu...

Senior Manager/Associate Director, Regulatory Strategic Planning Global Product Strategy, Regulatory Affairs As a leading global biopharmaceutical company, AbbVie is committed to addressing the world’s health challenges through the discovery, development and commercialization of advanced therapies and products that have a remarkable impact on people’s lives. As an AbbVie Regulatory Affairs (RA) ...

We have an exciting opportunity for an Assistant Director, CPPM Programming based in North Chicago, IL, for managing a Global Programming Team. The Clinical Pharmacology and Pharmacometrics(CPPM) Programming group is responsible for providing programming services to CPPM. The Assistant Director will manageand oversee a global team of SAS programmers responsible for creation ofdatasets appropriate...

As a leading global biopharmaceutical company, AbbVie is committed to addressing the world’s health challenges through the discovery, development and commercialization of advanced therapies and products that have a remarkable impact on people’s lives. As an AbbVie regulatory affairs (RA) professional, you’ll help safeguard the trust placed in AbbVie by ensuring that our products and practices adhe...

Statistics is responsible for providing services in the area of biostatistics and mathematics to all corporate divisions. These services are supplied in the context of a cooperative, project-oriented effort and included statistical planning and scientific input in general planning and execution of clinical trials, pre-clinical trials and other experiments as well as integration of all scientific e...

As an AbbVie regulatory affairs (RA) professional, you’ll help safeguard the trust placed in AbbVie by ensuring that our products and practices adhere to the highest quality and regulatory standards. Always with the patient in mind, the organization of Area and Affiliates Strategy continually designs and delivers optimized regional regulatory strategies, plans and dossiers that align with AbbVie’...

Baxter BioScience is a leading provider of therapeutic treatments that save, sustain and improve the lives of people with rare conditions, chronic diseases or limited treatment options. Supported by advanced technical and manufacturing expertise, Baxter BioScience has a broad pipeline built on a legacy of innovation in bleeding disorders and immunology and is expanding to address emerging opportun...

US Manager/Senior Manager Area and Affiliate - US and Canada (Oncology) Description Regulatory Affairs (RA) is the organization within AbbVie that ensures we comply with all regulations and laws pertinent to health care products. The regulatory function is vital to safety and effectiveness of health care products worldwide. Vision: With the patient in mind, be recognized as an Industry Leading ...

On March 27, 2014, Baxter announced plans to create two independent, publicly traded companies formed around the company's Medical Products and BioScience businesses. The company expects to complete this transaction in mid-2015, subject to market and regulatory approvals. Baxter's Medical Products business will remain a diversified company with a broad global footprint built around fluid systems,...

As an individual contributor, the function of the Associate Director Regulatory Affairs A&A– Project Management is to combine knowledge of scientific, regulatory and business issues to enable products are developed, manufactured or distributed to meet required legislation. The individual will provide project management capabilities to the Regulatory Affairs Area & Affiliate department. The individ...

Senior Medical Director, Product Safety Team Lead The Global Medical Services organization works collaboratively and strategically with colleagues across the product lifecycle to identify, evaluate, understand and communicate the safety profile of our drugs to protect patients worldwide. Key Responsibilities Include: Review clinical ICSR from current and on-going clinical trials and provide spo...

Senior Manager/Associate Director, Regulatory Strategic Planning Global Product Strategy, Regulatory Affairs As a leading global biopharmaceutical company, AbbVie is committed to addressing the world’s health challenges through the discovery, development and commercialization of advanced therapies and products that have a remarkable impact on people’s lives. As an AbbVie Regulatory Affairs (RA) ...

Description Baxter BioScience is a leading provider of therapeutic treatments that save, sustain and improve the lives of people with rare conditions, chronic diseases or limited treatment options. Supported by advanced technical and manufacturing expertise, Baxter BioScience has a broad pipeline built on a legacy of innovation in bleeding disorders and immunology and is expanding to address emer...

DescriptionOn March 27, 2014, Baxter announced plans to create two independent, publicly traded companies formed around the company's Medical Products and BioScience businesses. The company expects to complete this transaction in mid-2015, subject to market and regulatory approvals. Baxter's Medical Products business will remain a diversified company with a broad global footprint built around flu...