We are a pharmaceutical development company providing contract research services and monitoring instruments to emerging pharmaceutical companies and the world's leading drug development companies and medical research organizations. The Company focuses on developing innovative services supporting its clients’ discovery and development objectives for improved decision-making and accelerated goal attainment. The Company’s products focus on increasing efficiency, improving data, and reducing the cost of taking new drugs to market.

Responsibilities include:

• Responsible for all phases of protocol development; communicating with senior supervisory staff to establish study schedules as well as our clients to finalize the protocol and the technical staff to coordinate study initiation
• Direct and/or supervise the work of technical staff in accordance with the GLP’s 
• Monitor the progress of studies and after consultation with senior staff, report the results to the sponsor
• Participate in in-house training programs for the technical staff
• With the assistance of senior staff, prepare posters and/or scientific paper that will contribute to the scientific reputation the individual
• In consultation with senior staff, prepare reports, papers and/or charts of study data for interim reports to the sponsor
• Maintain knowledge of FDA and other regulatory guidelines that may affect protocol development
• Inform the management of any issues affecting the conduct of preclinical studies, interaction with clients and/or generation of protocols and reports
• Interact with the community and employees

Essential skills include

• Leadership; 
• Excellent written and verbal communication 
• Strong organizational skills
• Knowledge and experience with Good Laboratory Practice Regulations.
• Experience using computer applications; and data analysis skills 

Qualifications:

• This position requires a bachelor’s degree and 5 years of relevant experience or a master’s degree and 2 years relevant experience or a doctoral degree in one of the biological sciences and at least 1-year relevant laboratory animal experience

We are a contract research organization providing research and development resources to many of the world's leading pharmaceutical, medical device, and biotechnology companies. We offer an efficient cost-alternative to its client’s internal product development, compliance, and quality control programs. 

Our company benefits include a 401k and company match after 90 days, stock options, as well as relocation expenses.