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Senior Project Manager – west coast

This position is no longer available.

We are seeking an experienced project management professional to support Clinical Operations, Regulatory Affairs and Manufacturing with the planning and tracking of multiple new and ongoing projects. The incumbent will employ project management tools and methodologies to support and manage the development, coordination and ongoing tracking of multiple clinical and regulatory initiatives.

Qualifications include a proven track record of effectively applying project management tools and methodologies to manage and support the development, coordination and tracking of complex clinical and regulatory initiatives. As Senior Project Manager; you will interface daily with members of Clinical Operations, Regulatory Affairs and Manufacturing teams as well as external partners. Excellent communication skills are essential.  Other qualifications include a BS/BA  with 7+ years of experience in project management, 5+ years of project management experience in the pharmaceutical or life sciences space, expertise with project management software and other technical tools used in managing large projects, high proficiency with MS Office and ability to quickly master other software tools, Project Management Professional (PMP) Certification a big plus, proven ability to prioritize and execute tasks with minimal direction or supervision, work independently and meet tight deadlines in a fast-paced and demanding working environment, skilled in working with cross-functional project teams including Clinical Operations, Regulatory Affairs, Quality Assurance, Manufacturing and Marketing, excellent interpersonal, written and communication skills, exceptional analytical and problem-solving abilities, proactive self-starter with a roll-up-your-sleeves attitude, attention to detail and follow-through a must, general understanding of animal health product development and regulatory processes a plus.

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