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Research Fellow (Pharm Tech)
Pertinent Federal and State laws related to Pharmaceutical industry; current FDA, Drug Enforcement Agency and Regulatory Affairs clinical requirements and cGMPs.
Pharmaceutical research techniques and methods; medical terminology and treatment modalities and trends.
Clinical studies design and principles of trial management.
Project management principles and techniques.
Business, scientific and personal computer hardware and software applications.
Business English usage, spelling, grammar and punctuation.
Current Company policies, practices and procedures, including safety regulations.
Implementing strategic plans, goals, objectives and practices for effective, efficient and cost effective management of allocated resources.
Preparing and presenting information to medical, public, technical and scientific groups.
Analyzing problems; identifying alternative solutions; projecting consequences of proposed actions; and implementing recommendations.
Communicating clearly and concisely, both orally and in writing.
Managing multiple projects, duties and assignments.
Interpreting and applying Federal, state and local policies, procedures, laws and regulations.
Establishing and maintaining cooperative working relationships with others. Incumbents in this class are subject to extended periods of sitting, standing, walking, and vision to monitor, and moderate to loud noise levels. Incumbents may be exposed to toxic materials, toxic gases, electrical hazards, dangerous tools and equipment and the antibiotics penicillin and cephalosporin. Work is performed in office and laboratory environments.
Ph.D., M.D. or Pharmaceutical Doctorate Degree from an accredited college or university, and six (6)) years pharmaceutical clinical experience, or an equivalent combination of education and experience, including at least two (2) years at the director level. Pharmaceutical industry experience preferred.
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