Our client is a development-stage, specialty pharmaceutical company that focuses on drugs used in the treatment of autoimmune diseases and central nervous system diseases. The company has an experienced management team and a large number of products in the late stages of clinical trials. This is a strong opportunity for someone that wants to put their drive and initiative to work.

Job Responsibilities:
1) General oversight of company, specifically in clinical development
2) Supervise all clinical trials being run
3) Manage and direct operations along with the Clinical, QA, QC and Regulatory operations for the Florida site
4) Plan (strategically), prepare and implement annual budgets
5) Ensure full compliance with GCP/GMP requirements
6) Ensure that the company maintains a qualified, well-trained staff
7) Oversee quality program to ensure continuous process improvement
8) Encourage communication and efficient cooperation across departments and company sites
9) Oversee logistics for project planning, cost control and supply of materials for production
10) Handle maintenance of buildings and equipment

Job Requirements:
1) Well-organized, highly motivated and action-oriented team player
2) Extensive background in oversight of phase III clinical trials
3) Experience with operations for the successful development of new drugs for a small company
4) Experience in the regulatory environment for the pharmaceutical business
5) Excellent problem-solving and interpersonal skills
6) Strong hands-on managerial and leadership skills
7) Working knowledge of pharmaceutical Quality Assurance

Applicants are encouraged to apply directly by going to: http://www.sterlinglifesciences.com/jobs/lifesciences-jobs-03464.html