Study Director IV

Inotiv • Boulder, CO

4d • Onsite

About The Position

The position has responsibilities centered around the execution, planning, and management of assigned studies. The role will participate in in vivo pharmacology research conducting biochemical screening models, proof-of-concept models for target validation, as well as disease efficacy models to evaluate development and discovery lead compounds. The ability to communicate succinctly with clients, coordinators, and technicians is key as well as a cross-functional, flexible, and collaborative spirit. This position could be offered at different levels for candidates who qualify with a combination of advanced levels of education and/or years of experience. The salary range will adjust along with the level of the role to match the person’s relevant experience and/or education level. Inotiv is a growing contemporary drug discovery and development company where we “Play to Win” in an industry rich with opportunity. Together, we face challenges and together we win in the delivery of world-class drug discovery and development solutions that impact the health and well-being of people all over the world. There’s an opportunity for everyone at all phases of a career, each individual’s unique skill set has an impact on the work we conduct. If you have the talent and desire to impact the quality of people’s lives, we have the career opportunities to make it happen. Join us in embracing research and science to impact the health and well-being of people all over the world. As a leading contract research organization (CRO), Inotiv supports discovery and nonclinical development through investigational new drug (IND) and beyond. By leveraging our deep expertise and scientific capabilities, we help you increase efficiency, improve data, and reduce the cost of taking new drugs to market. By providing critical research models and related services, we help researchers realize the full potential of their R&D projects, all while working together to build a healthier and safer world. We hope you consider our opportunities and a future with Inotiv!

Requirements

• A basic understanding of integrated physiology, pathophysiology, and pharmacology is required.
• Previous pre-clinical in vivo laboratory experience including handling of research rodents is required.
• MS degree in related scientific discipline (e.g., Physiology, Pharmacology) and at least 10+ years of experience of related experience or an equivalent combination of education and experience is required
• Commitment to safety and the humane treatment of laboratory animals is required.

Nice To Haves

• Industry research experience is highly preferred.
• Research experience in therapeutic area is highly preferred.
• Ph.D. degree in related scientific discipline (e.g., Physiology, Pharmacology) is highly preferred.
• Experience with rodent survival surgeries is desired.

Responsibilities

• Manages client correspondence and relationship
• Works with study sponsors to create study protocols
• Informs Live Phase Study Coordinator of decisions to initiate studies and thereby proceed with ordering animals and necessary study supplies
• Ensures all research technicians are properly trained to perform task and is ultimately responsible for all work performed on his/her study.
• Performs disease-inducing procedures
• Provides potential study sponsors with quotes for proposed studies
• Ensures all tasks are performed on daily schedule
• Performs surgical procedures
• Performs research technicians’ tasks, as needed
• Prepares high quality and accurate data package for clients
• Keeps track of project timelines for forecasting purposes
• Oversees coordinating of all studies and allocates resources
• Identifies and is accountable for driving ways to improve the efficiency and quality of processes and the resulting deliverables, influencing key stakeholders as applicable
• Writes IACUC protocols
• Manages direct reports which entails technical training as well as career growth and development
• Strategic thinking around process improvement, business development, and overall study operations
• Other duties may be assigned

Benefits

• health and dental coverage
• short- and long-term disability
• paid time off
• paid parental leave
• 401K

What This Job Offers

• Job Type: Full-time
• Career Level: Senior