Clinical Trial Manager, Veterinary Medicine
At Elanco (NYSE: ELAN) – it all starts with animals!
As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets.
We’re driven by our vision of ‘Food and Companionship Enriching Life’ and our approach to sustainability – the Elanco Healthy Purpose™ – to advance the health of animals, people, the planet and our enterprise.
At Elanco, we pride ourselves on fostering a diverse and inclusive work environment.
We believe that diversity is the driving force behind innovation, creativity, and overall business success.
Here, you’ll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights.
Making animals’ lives better makes life better – join our team today!
Your Role: Clinical Trial Manager, Veterinary Medicine
This position will function in the efficient and effective management and execution of clinical studies.
The individual will be responsible for continuing to grow and develop capabilities in clinical trial implementation.
The incumbent will coordinate, oversee, and monitor clinical studies needed for the registration of global products for Elanco. The individual will maintain an excellent working knowledge of government regulations and policies pertaining to clinical trials, VICH-GCP guidelines, company Standard Operating Procedures (SOPs), and assigned study protocols.
The position will interact with US research scientists and the global research and development teams to gain regulatory approval of these products.
Your Responsibilities:
* Plan, manage, and coordinate all phases of clinical trial activities, including study initiation, execution, and close-out.
* Support study teams by reviewing protocols, final reports, and assisting with data capture design and QA/audit responses.
* Perform or oversee monitoring duties, site recruitment, training, and compliance across assigned clinical sites.
* Collaborate cross-functionally across R&D, commercial, and external partners to drive project execution and alignment.
* Support budgeting, contracting, and invoicing efforts, and contribute to accurate project forecasting.
* Contribute to a high-performing, innovative team culture aligned with Elanco values and behavioral pillars.
* Participate in regulatory inspections (FDA/USDA) and communicate effectively with regulators, as needed.
* Mentor study monitors and administrators, and take on additional tasks as directed by leadership.
* Identify risks and implement proactive solutions to ensure timelines, quality, and compliance targets are met.
* Drive continuous improvement by evaluating study operations and recommending efficiencies in trial conduct and data quality.
* Ensure adherence to internal SOPs and evolving regulatory requirements acros...
- Rate: Not Specified
- Location: Greenfield, US-IN
- Type: Permanent
- Industry: Medical
- Recruiter: Elanco
- Contact: Not Specified
- Email: to view click here
- Reference: R0022960
- Posted: 2025-07-31 09:14:19 -
- View all Jobs from Elanco
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