Pharmacology Director Jobs in Illinois
Director, Regulatory Affairs CMC Chicago Description Primary Function • Lead a team of global regulatory professionals who develop strategy for development and marketed products, and manage the content of global regulatory dossiers • Key internal leader and driver of regulatory policy and strategy • Influence the development of regulations and guidance • Provide executive management with meaningfu...
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...
Director Regulatory Affairs, Area & Affiliate US/Canada- Chicago PRIMARY JOB FUNCTION: Candidate will be responsible for contributing to and implementing strategies to support assigned projects within Therapeutic Area (e.g., HCV). CORE JOB RESPONSIBILITIES: • Review, compile, and submit variations, new applications, supplements and amendments, as well as responses to Health Authorities as needed •...
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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.
Manages human resource accomplishments by recruiting, selecting, orienting, and training staff members; assigning responsibilities; identifying, selecting, and monitoring contract research organizations (CROs); coaching, counseling and disciplining employees; planning, monitoring, and appraising job results.
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