
Animal Health Clinical Research Associate
Argenta
Mumbai, Maharashtra, India
Information Technology, Science / R&D / Research, Analyst
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.
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.
Our US Clinical team is looking for experienced, motivated, driven individuals who thrive in their ability to multitask and work as a team!
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 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 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 all serious AEs and non-serious AEs 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 beyond
- Minimum of 5 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. 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 and analytically driven
- Willingness to travel, expected to travel nationally 40 to 60%
This role is subject to a DEA background check as well as a pre-employment drug screen and/or physical.
Argenta is an equal opportunity employer
To find out more about Argenta, click here: www.argentaglobal.com
About the company
Company website•Pharmaceutical Manufacturing
At Argenta, we’ve been collaborating with clients worldwide since 2006, bringing expertise, innovation, and a can-do attitude to deliver cutting-edge animal health & nutrition, and human nutrition solutions.
Why Argenta?
We are the only global CRO and CDMO focused exclusively on animal health & nutrition, complemented by regulatory expertise in human nutrition. We provide tailored, end-to-end solutions from Molecule to Market at any scale.
Our Three Pillars:
• Global Partnerships – turning ideas into reality worldwide
• Molecule to Market Approach – guiding products from research to launch
• Innovation – driving progress in animal & nutrition, and human nutrition
Our Services:
• R&D: innovative animal health & nutrition solutions, fully EMA/FDA/EFSA compliant
• Pre-Clinical Research: dedicated teams in Spain, Germany, and the US providing confident go/no-go decisions
• Clinical Research: agile, high-quality veterinary studies delivered on time and within budget
• GMP Manufacturing: facilities in New Zealand, the US, and the UK
• Regulatory & Scientific Consultancy: expert support for medicinal products, feed additives, and human nutrition products (novel foods, food additives, enzymes, etc)
• Full Product Development: from concept to market
Collaboration at Our Core:
950+ experts in science, veterinary, engineering, and regulatory affairs, working closely with clients to develop products that truly make an impact.
Our Story:
Founded in New Zealand by scientist Doug Cleverly, Argenta combines Kiwi ingenuity with global collaboration. Our roots as a trusted CRO go back to 1987, built on scientific excellence and long-term partnerships.
Today, through our CMO & CDMO facilities, we optimize efficacy trials, accelerate product development, and help companies turn innovative ideas into market-ready products.
We also support human nutrition projects, guiding companies through regulatory pathways to successfully launch new products.
Let’s make it happen - together!