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Veterinarian, Clinical Research Associate
2 months ago
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 organisation (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.
With bases in New Zealand, the US, the UK and Europe, our 650+ 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 looking for an experienced Veterinarian, Clinical Research Associate (VCRA) to join our Clinical RD&I team.
The Veterinarian, Clinical Research Associate adds value through the following responsibilities:
- Coordinates and conducts GCP and study protocol training at study sites and assures training is documented
- Builds rapport with study site staff to assure compliance with the protocol, applicable regulatory and guidance documents, SOPs, and all study activities
- Assists in reviewing the study records and all study notebooks to ensure contents are current and complete
- Assists in providing tracking and Quality Control (QC) of data as required and assists with responses to QA audits
- Evaluates Investigators and assists with selection of appropriate sites to conduct clinical studies
- Collaborates with the study Project Manager to assure study sites selected meet the needs of the study protocol
- Monitors assigned study sites through review of electronic data capture (EDC) systems, faxed, emailed, and paper documentation.
- Serves as the liaison between Argenta Clinical and study site personnel
- Tracks adverse events (AE's) encountered in clinical studies and ensures all serious AEs and non-serious AEs are documented and communicated appropriately to the Project Manager and Sponsor
- Acts as Safety Monitor for medically complex studies
- Learns to assist with facilitates clarifications, corrections, and data query resolution with study sites or data management personnel
- Builds relationships with key individuals and contributors in the organization and beyond
- Doctor of Veterinary Medicine Degree from accredited university program or equivalent degree
- Current and active veterinary license, in good standing
- Minimum of 2 years' experience in a scientific discipline and/or veterinary experience
- Experience in Good Clinical Practice (GCP) data management, quality control, and/or quality assurance preferred
- Collaborative working style. Lead and motivate people through influence across all levels and functions of the organization
- Ability to look for creative solutions to resolve complex issues
- Strong technical writing ability
- Results oriented and driven
- Strong communication and listening skills
- Well organized
- Willingness to travel, expected to travel nationally up 40 to 60%
Why us?
Argenta has strongly embedded company values which is key to who we are and how we deliver. 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.
For more information go to www.argentaglobal.com
Equal Opportunity Employer