Study Director IV

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.

• 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

• 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.

• Industry research experience is highly preferred.

• Research experience in therapeutic area is highly preferred.

• 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

• Ph.D. degree in related scientific discipline (e.g., Physiology, Pharmacology) is highly preferred.

Skills

• 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.

• Experience with rodent survival surgeries is desired.

• 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.

• Results Driven: Internal drive toward action to efficiently, timely, and accurately achieve results. Sets high but achievable standards for self and others. Seeks opportunities to improve process and outcomes. Constantly reviews performance to identify areas to develop.

• Customer Focus: Identifies, prioritizes and anticipates customer needs and delivers relevant, value-add, solutions to meet and exceed them.   

• Efficient:  Takes responsibility for own time and effectiveness.  Identifies what needs to be done and does it before being asked or before the situation requires it.  Able to work things out without having to be shown too often. Seeks opportunities to contribute appropriately without direction. 

• Communication:   Able to communicate information and ideas clearly and articulately both in oral and written form. Uses appropriate language, style and methods depending on audience and the purpose of communication. Able to convey complex information clearly. Anticipates the information that others will need. Expresses ideas effectively.  Practices attentive and active listening.

• Collaboration:  Actively supports and contributes to the success of the team. Actively encourages and practices collaboration and cooperation on the team.  Shares information and supports other team members. Can get things done with and through others and set realistic objectives. Seeks opportunities to develop others.

• Critical Thinking and Problem Solving: Able to identify and separate out the key components of problems and situations. Able to manipulate and interpret information from a range of sources to spot patterns and trends in information and to deduce cause and effect from this. Can generate a range of creative solutions, evaluate, and choose the most appropriate option.

• Organization and Time Management: Plans and prioritizes work, manages time appropriately to meet deadlines, follows up with others to ensure one’s own work and commitments are completed on time, deals with pressure and deadlines through good planning.

Working Conditions & Physical Requirements

• Work is performed in a typical interior office

• Prolonged periods of sitting at a desk and computer work

• Work also conducted in laboratory setting

• Teamwork setting

• Consistent written and verbal communication

*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.

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.