Senior Clinical Research Associate (CRA) – Animal Health
Quick Summary
Oversee the monitoring and execution of farm and companion animal clinical trials, ensuring all activities comply with global regulatory standards (GCP/VICH) and internal policies.
Requirements
~1 min read- Education & Experience: A Bachelor's degree in a science or health-related field with 5+ years of applicable experience, OR a Master’s degree in a science or health-related field with 3+ years of applicable experience.
- Clinical Trial Experience: Proven experience monitoring single-site or multi-site clinical field studies for safety and effectiveness.
- Key Skills: Demonstrated interpersonal skills with the ability to work within and across interdisciplinary teams, combined with a strong knowledge of animal health concepts and global clinical trial regulations.
- Direct experience with regulatory authority submissions and a deep understanding of the data requirements for successful filings.
- Experience acting as a lead monitor or mentor for other Clinical Research Associates on clinical projects.
- Advanced proficiency in clinical trial management systems, such as Veeva Vault, and other collaborative tools.
- Specialized experience in either Farm Animal or Pet Health clinical studies.
- Proven ability to anticipate issues and proactively ensure innovative solutions in a fast-paced, matrixed environment.
Responsibilities
~1 min read- →Oversee the monitoring and execution of farm and companion animal clinical trials, ensuring all activities comply with global regulatory standards (GCP/VICH) and internal policies.
- →Author and execute comprehensive monitoring plans; conduct site qualification, initiation, routine monitoring, and close-out visits in accordance with study requirements.
- →Perform thorough data review (QC) and query resolution to ensure the highest level of data integrity and quality across all assigned studies and projects.
- →Serve as the primary contact for investigator sites and third-party organizations (CROs), overseeing study site documentation, investigational material shipments, and drug accountability.
- →Collaborate with cross-functional partners, including Regulatory Affairs and Data Management, to support protocol development, study planning, and the development of final study reports and submission files.
- Travel: Up to ~50%
- Location: US - Teleworker
Don’t meet every single requirement? Studies have shown underrepresented groups are less likely to apply to jobs unless they meet every single qualification. At Elanco we are dedicated to building a diverse and inclusive work environment. If you think you might be a good fit for a role but don't necessarily meet every requirement, we encourage you to apply. You may be the right candidate for this role or other roles!
What We Offer
~2 min readWe offer a comprehensive benefits package focusing on financial, physical, and mental well-being while encouraging our employees to pursue our purpose!
Some highlights include:
Location & Eligibility
Listing Details
- Posted
- October 9, 2026
- First seen
- October 10, 2026
- Last seen
- October 10, 2026
Posting Health
- Days active
- 0
- Repost count
- 0
- Trust Level
- 65%
- Scored at
- October 10, 2026
Signal breakdown
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