Pharmacology Director Jobs in Illinois
Senior Director, Regulatory Affairs, Area & Affiliates US & Canada Description Primary Job Function: The function of a Senior Director Regulatory Affairs is to combine knowledge of scientific, regulatory and business issues to enable products that are developed, manufactured or distributed to meet required legislation. Additionally, the individual may develop and supervise regulatory professionals...
Discover a new kind of career with a new kind of industry leader. Discover Hospira, a specialty pharmaceutical and medication delivery company driven to improve the safety and effectiveness of patient care for millions worldwide. Our story is one of integrity, entrepreneurial spirit, agility, and accountability. It has developed over 70 years defined by rich discoveries, progressive energy, and ma...
Under direction of the Medical Director, serves as an Advanced Practice Nurse (APN), with responsibility for individual patient care, as well as responsibility addressing broader geriatric healthcare issues. As a certified nurse practitioner, conducts physical examinations, takes medical histories, performs diagnoses of, and treats common acute minor illnesses or injuries and stable chronic illnes...
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Education: - BS from Yale; Chemistry -PhD from UNC; Pharmacology Job Title: Director-Clinical Research and Development for Pfizer New York.
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Healthcare Career Tools
$87,360.00 - $250,000.00
Typical Salary for Director-Pharmacology in Illinois
Source: Monster.com Careerbenchmarking Tool
Education / Training
Some College Coursework Completed
Source: Monster.com Careerbenchmarking Tool
Develops therapeutic strategies by establishing, developing, implementing, and controlling pre-clinical studies of candidate pharmacological compounds; validating outcomes; managing staff.
Rate of Growth
Size of Industry in 2006:
Source: Bureau of Labor Statistics, May 2006
Dealing with Complexity
Controls pre-clinical study plan by establishing and approving methods for design and implementation of clinical in vivo and in vitro protocols involving pharmacokinetics, metabolism, and bioavailability, data maintenance systems, data evaluation, and reporting; enforcing adherence to development plans, Food and Drug Administration (FDA) guidelines and regulations, good clinical practice (GCP), organization policies, and standard operating procedures (SOPs); interpreting and evaluating clinical data; analyzing safety and other pharmacology data; reviewing open issues; communicating essential information.
Maintains clinical data base by developing information requirements; designing standards for an information system; monitoring data entry and maintenance.
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