Study Director - Americas CRO

Argenta•Oakland, NE

2d•Onsite

About The Position

At Argenta, we’re more than a company — we’re a global team, dedicated to healthier animals. We believe that when their lives are made better, we're all the better for it. Founded in 2006, we support companies big and small to develop and manufacture health products for pets and livestock. Our trusted, innovative solutions and services cover every stage of the process, from molecule to market. We’re in a unique position. We are the world’s only combined contract research and contract development and manufacturing organization (CRO/CDMO) dedicated to animal health. Our uniqueness means: We are ambitious, growing and building a ‘one team’ culture, guided by our values. We are team players; We are doers; We are customer-centric; We are innovators. We value diversity, as a global company, we get the richness of working with different people in different places whether it be location, stages of their career, their development, their role. We believe that when everyone works together and puts their best “paw” forward we will make the lives of the animals we care for, better. With bases in New Zealand, the US, the UK and Europe, our 900+ colleagues are driven by our partnership approach and purpose: Healthy Animals. Let’s Make It Happen, Together. TEAM PLAYERS who want to DO great work and find INNOVATIVE ways to make animals lives better through our CUSTOMER CENTRIC efforts should apply. Argenta is currently looking to fill the role of Study Director at our Oakland , NE location.

Requirements

Advanced degree in a scientific discipline.
10+ years experience in animal health product development, or veterinary clinical study project management.
Proven experience managing cross functional teams
Thorough knowledge of practical experience in GLP protocols, Final Study Reports and Study Master Files
Collaborative working style and the ability to lead and motivate people at all levels and across multiple functions within the organization
Proven affinity with Animal Health
Excellent attention to detail and scientific judgement

Responsibilities

Approve and sign study protocol
Ensure objectives meet regulatory requirements
Coordinate with Sponsors and Quality Assurance
Delegates tasks accordingly during the course of the study but retails full responsibility
Ensures the study follows GLP and study protocol, overseeing animal care, sample collection and data recording
Addresses deviations and ensures proper documentation
Review and interpret results ensuring the scientific validity of conclusions
Writes, approves and signs the final study report
Ensures all raw data are archived properly