Study Director I

Inotiv•Westminster, CO

13d

About The Position

The position has responsibilities centered around the execution, planning, and management of assigned studies. The role will participate 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. 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. Salary will be commensurate with experience and responsibilities. Benefits include health and dental coverage, short- and long-term disability, paid time off, paid parental leave, 401K, and more! Inotiv is an Equal Opportunity Employer. It is our policy to provide a fair and equal employment opportunity to all persons, regardless of age, race, color, religion, sex, gender, gender identity, gender expression, sexual orientation, genetic information, disability, national origin, veteran status, or any other basis prohibited by law. This policy governs all aspects of employment, including selection, job assignment, compensation, discipline, termination and access to benefits and training.

Requirements

To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required.
An individual with an in-depth understanding of in vivo models of multi-system rodent physiology and in vitro analyses of pathobiology and disease biomarkers.
Demonstrates strong organizational, communication (both oral and written), time management, and interpersonal skills in a cross-functional team.
Must actively participate and work well in a collaborative, team-oriented environment.
Should be adept at data management and reduction.
Able to demonstrate strong skills in authoring and managing the production of scientific documents (e.g., pre-clinical study protocols, data package, technical reports, publications in peer-reviewed journals).
Proficient with Microsoft Excel, Word, and PowerPoint; familiarity with GraphPad Prism desired.
Shows flexibility and ability to apply his/her knowledge to new areas of study.
Commitment to safety and the humane treatment of laboratory animals is required.
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 3-8 years of related experience or an equivalent combination of education and experience is required.

Nice To Haves

Experience with rodent survival surgeries is desired.
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.

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 as needed, and as trained
Provides potential study sponsors with quotes for proposed studies
Ensures all tasks are performed on daily schedule
Performs surgical procedures as needed, and as trained
Performs research technician level tasks as needed, and as trained
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
Perform other duties as assigned