Consultant - R&D Support

• DVM and/or PhD with 2+years clinical research operations experience, scientific writing or study support. 
• Understanding of FDA, USDA, EMA, ICH, GLP and GCP guidelines.
• Proven track record showing clear proficiency in clinical project management skills.
• Proven complex problem-solving skills.
• Understanding of clinical operations related to clinical development functions.
• Detailed understanding of all aspects of clinical protocol design and implementation & overall drug development.
• Ability to effectively interface with clinical personnel at internal and external clinical site(s).
• Ability to collaborate effectively with global teams in the USA, EU and Australia
• Ability to write and edit technical documents, such as protocols, protocol amendments,
• Detailed and team oriented with excellent cross-functional team leadership and participation skills.
• Excellent interpersonal, verbal and written communication skills (English) are essential in this collaborative work environment.
• Proficiency with computer programs including CTMS and document management (Veeva), Microsoft Office suite and Microsoft Project.

Elanco is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status

Elanco may use automated tools, including AI, to support parts of our recruitment process, such as reviewing applications against job‑related criteria and/or transferrable skills. These tools help ensure a consistent, structured evaluation, but they do not make hiring decisions. All decisions involve a human reviewer. For more information on how we handle personal data, please see our Elanco Workforce Privacy Notice.

Responsible for driving clinical trial and project acceleration through scientific authoring, study support, remote site master file oversight, material shipment coordination, and technical system management. This role will report, via dotted line, and support Sponsor Representatives (SRs) and Global Clinical Leads (GCLs) by performing remote study support activities to ensure data integrity, maintaining the primary R&D systems (e.g., Veeva Platform) for global visibility, and managing the end-to-end lifecycle of study documentation and tracking.

·       SR and Global Clinical Lead Support: Conducts remote support activities and study oversight to ensure compliance and data quality. Acts as a remote extension of the clinical team to identify and resolve or escalate study issues.

·       Document Management: Managing document transfer for data entry and/or corrections.  Manages the real-time digital assembly, QC, and maintenance of the Study Master File (SMF/TMF). This may include APEX systems or working environments such as SharePoint.  Ensures all internal documents adhere to Elanco guidelines and regulatory templates.

·       Primary R&D System Maintenance: Serves as the primary lead for primary system updates (study tracking, project management, document management and budgets), ensuring all study parameters, site data, and project milestones are accurately maintained and audit-ready.

·       Study Tracking: Proactively tracks global study milestones and deliverables, providing GCLs with critical path visibility and status reporting.

·       Scientific Authoring: Prepares regulatory and scientific documents, including protocols, Final Study Reports (FSRs) and other study related documentation, abstracts, summaries and manuscripts.

·       Operational Support: Manages site contracting (Procurement interface) and oversees in-life AE/PV reporting requirements (including threshold detection) to meet global regulatory timelines.

·       IVP Management: Support and partnership with internal Technical Project Leads (TPL’s), GCL’s and R&D material management to ensure timing, requirements, and documentation are coordinated for IVP material shipment.