Senior Product Development Manager

Argenta • Shawnee, KS

8h

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. The Americas CRO team is looking for motivated, driven individuals who thrive in their ability to multitask and work as a team! Argenta, Americas CRO is currently looking for a Senior Product Development Manager to join our team. The Senior Product Development Manager adds value through the following responsibilities: Supports the Americas CRO business (regulatory to pre-clinical to clinical service) needs of Argenta Molecule to Market, and Risk/Mitigation plans Effectively manage the product development requirements (pre-clinical and clinical projects) of internal and external projects Demonstrates an awareness of current regulations, guidance's, and the animal drug development process, while maintaining a flexible and creative mindset to work through product development challenges. Contribute to the development of business strategies to increase profitability and grow the business to create value. Manage development projects or key development project areas from initial conversations to live-phase study activities to close-out / final study report signatures to tracking overall timelines and budgets for study activities. Coordinates selection of the vendor(s) for study protocol conduct &/or laboratory requirements and activities including the provision of necessary supplies required by the study protocol Provides oversight to ensure tasks are completed correctly and on time (i.e. oversight in the tracking of adverse events (AEs) encountered in the study and ensures that all serious AEs and non-serious AEs are communicated appropriately to the Sponsor) Coordinates the creation of materials and documentation for the study, and QA resources, as required Directs and provides oversight of investigational veterinary product/control product inventory, accountability, labelling, regulatory documentation/notifications, and shipment of drug supplies to/from the Sponsor and study sites

Requirements

• 10+ years or greater in veterinary drug development
• Clinical Research Associate experience or equivalent experience and training
• Experience and skills necessary to monitor a study
• Results oriented. Defines and plans priorities well
• Effectively manage client and stakeholder expectations through relevant communication
• Comfortable balancing shifting priorities as required to meet business needs
• A collaborative working style to be able to lead and motivate people at all levels and across all functions in an organization
• Strong analytical thinking and problem-solving skills
• Capable of working in a changing environment and under pressure
• Effectively present information and concepts, in both written and oral formats clearly and concisely
• Actively listens to ensure understanding
• Computer proficiency including Outlook & Microsoft Suite and various assigned database platforms and electronic meeting applications
• Express facts and ideas in writing in a clear, concise, convincing, and organized manner

Responsibilities

• Supports the Americas CRO business (regulatory to pre-clinical to clinical service) needs of Argenta Molecule to Market, and Risk/Mitigation plans
• Effectively manage the product development requirements (pre-clinical and clinical projects) of internal and external projects
• Demonstrates an awareness of current regulations, guidance's, and the animal drug development process, while maintaining a flexible and creative mindset to work through product development challenges.
• Contribute to the development of business strategies to increase profitability and grow the business to create value.
• Manage development projects or key development project areas from initial conversations to live-phase study activities to close-out / final study report signatures to tracking overall timelines and budgets for study activities.
• Coordinates selection of the vendor(s) for study protocol conduct &/or laboratory requirements and activities including the provision of necessary supplies required by the study protocol
• Provides oversight to ensure tasks are completed correctly and on time (i.e. oversight in the tracking of adverse events (AEs) encountered in the study and ensures that all serious AEs and non-serious AEs are communicated appropriately to the Sponsor)
• Coordinates the creation of materials and documentation for the study, and QA resources, as required
• Directs and provides oversight of investigational veterinary product/control product inventory, accountability, labelling, regulatory documentation/notifications, and shipment of drug supplies to/from the Sponsor and study sites

Benefits

• We offer an opportunity to work for a successful and rapidly expanding global business where your input will be valued.
• At Argenta we are a hard-working group who really enjoy the people we work with each day. That is why we support our people through strong culture, great benefits, and opportunity for growth.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Education Level: No Education Listed