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Job #02405

About our client Our client focuses on research and development of biopharmaceutical products. Their products are mainly based on their patented DNA delivery technologies for the prevention and cure of serious or life-threatening diseases. The company has access to enhancing technologies with the help of license and collaborative agreements. Position Location Associate Project Manager Southern California Salary Highly competitive package, commensurate with experience Responsibilities 1) Assist the Executive Director in planning and implementation of safety and efficacy studies required for IND submissions and licensure of products 2) Work in conjunction with study directors at CROs and/or academic institutions 3) Prepare and implement protocols necessary for safety and efficacy studies 4) Act as a liaison between departments 5) Represent PS&E Department on project team and report back to Executive Director 6) Monitor internal and external studies, compilation and appropriate presentation of date, including statistical analysis 7) Ensure that internal and external reports are written accurately and submitted in a timely manner Requirements 1) Ph. D in Toxicology, Pharmacology, or a related field or MS/BS 2) M.Sc preferred 3) Immunology preferred 4) Pharmacology/toxicology experience preferred 5) 3-5 years of experience in safety and efficacy studies in pharmaceutical or biotech industries 6) 5+ years of experience 7) Experience in working with a variety of animal models preferred 8) Experience in project management 9) Safety experience preferred 10) Pre-clinical experience preferred 11) Regulatory experience preferred 12) Strong leadership skills and ability to be a team player 13) Willingness to travel