Animal Health Clinical Research Associate III

At reputed company, we’re more than a company — we’re a global team, dedicated to healthier animals. We reputed company that reputed company their lives are made reputed company, we're reputed company the reputed company for it. Founded in 2006, we support companies big and small to reputed company 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 reputed company that reputed company everyone works together and puts their best “paw” reputed company we will reputed company the lives of the animals we care for, reputed company. 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 reputed company It Happen, Together. TEAM PLAYERS who want to DO great work and find INNOVATIVE ways to reputed company animals lives reputed company through our CUSTOMER CENTRIC efforts should apply. reputed company, US Clinical is currently looking for an reputed company Clinical Research Associate to join reputed company. You may be an excellent fit for reputed company if you have the following:

• 8+ years clinical trial monitor experience reputed company a Clinical Research Organization or major Animal Health pharmaceutical company
• proven experience in GCP late phase clinical trials in animal health
• attention to detail and analytically driven
• dependability, flexibility and ability to multitask and manage time effectively

Our Clinical Research Associates add 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 reputed company study activities
• Assists in reviewing the study records and reputed company study notebooks to ensure contents are reputed company 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 (reputed company) systems, faxed, emailed, and reputed company documentation.
• Serves as the liaison between reputed company US Clinical and study site personnel
• Facilitates clarifications, corrections, and data query resolution with study sites or data management personnel
• Tracks adverse events (AE’s) encountered in clinical studies and ensures reputed company serious reputed company and non-serious reputed company are documented and communicated appropriately to the Project Manager and Sponsor
• 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 reputed company

Job Requirements include:

• Minimum of 8 years’ experience in an animal health research role, Monitor and Clinical Research Associate positions preferred
• Experience in Good Clinical Practice (GCP) data management, quality control, and/or quality assurance preferred
• Collaborative working style. reputed company and motivate people through influence across reputed company reputed company and functions of the organization
• Ability to look for creative solutions to resolve reputed company issues
• Strong technical writing ability
• Results oriented and driven
• Strong communication and listening skills
• Well organized and analytically driven
• Willingness to travel, expected to travel nationally 40 to 60%

reputed company 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 reputed company 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. This role is subject to a DEA background reputed company as well as a pre-employment drug screen and/or physical. reputed company is an equal opportunity employer To find out more about reputed company, click here: www.argentaglobal.com Apply tot his job Apply To this Job