About the role
Product Development Program Manager - Animal Health
Location: Remote – North America or Europe | Reports to Chief Commercial Officer (UK)
Division: Business Development
The Opportunity We are seeking an experienced Product Development Program Manager to support Business Development efforts with entry-level Sponsors and to develop and manage Product Development Programs. This remote role (North America or Europe) will serve as a primary contact and coordinator across the Clinglobal Group’s strategic business units and external partners, ensuring high-quality, timely, and compliant delivery of development programs.
The successful candidate will provide initial guidance on animal care product development, assess the Group’s capability to support all or part of a program, coordinate input across SBUs, manage program plans and systems, and support the timely preparation of quotes and proposals.
About Clinglobal
Clinglobal is an Animal Health Contract Research Organization (CRO) and member of the Clinglobal Group. We accelerate animal health innovation through a unique model that combines streamlined contracting, centralized project and program management, and a broad portfolio of preclinical, clinical, regulatory, data science, and laboratory services delivered by our group companies and strategic partners.
Animals are our passion; people are our strength. Together, we better lives by accelerating animal health innovation.
Key Responsibilities
The responsibilities listed below highlight the main focus areas of the role. The full job description, including all duties, expectations, and detailed requirements, will be shared and discussed during the interview process.
* Serve as the primary Lead Manager for Sponsors, helping identify needs, priorities, and constraints (regulatory, ethical, economic, or other). * Liaise with Clinglobal Group strategic business units to gather feedback, provide Sponsors with preliminary guidance, and ensure enquiries are adequately handled. * Act as the primary project contact with Sponsors, maintaining communication and reporting schedules. * Coordinate resources across SBUs and departments to achieve project outcomes on time. * Develop and oversee project management plans for company projects and product development programs. * Coordinate programs across phases (formulation, safety, efficacy, regulatory/registration), managing relationships with internal teams, external partners, and vendors. * Ensure full project life-cycle completion and delivery of outcomes according to timelines, quality, and cost. * Provide regular status reporting to management and Sponsors (including budgets and timelines) via project review meetings. * Proactively identify and manage risks related to feasibility, resources, execution, and budget. * Develop and maintain project management tools (Gantt charts, budgets, forecasts, risk registers, etc.). * Mentor and train team members on Program Management principles. * Promote Clinglobal’s capabilities and values internally and externally. * Represent the Group at industry events, conferences, customer meetings, and professional associations
Requirements
* Degree in a related Life Sciences discipline. * Minimum 10 years’ experience in animal health drug/product development. * Strong industry expertise including working knowledge of FDA CVM, EMA, VMD, GRP, GLP, GCP, VICH Guidelines, pre-clinical regulatory requirements, clinical field studies, and data quality requirements. * Global regulatory experience, including authoring submission documents, responses to questions, scientific advice, and in-person interactions. * Exceptional organisational, project, and program management skills. * Strong technical writing and oral presentation skills. * Fluency in English (additional languages an advantage). * Ability to work effectively across time zones with a UK-based reporting line and global stakeholders. * Willingness to travel occasionally for Sponsor meetings, audits, and partner visits.
Work Environment
This is a remote role based in North America or Europe. The employee will primarily work at a desk/computer during normal business hours, with flexibility for after-hours, evenings, weekends, or public holidays according to pre-arranged schedules. Occasional travel is required.
Important Note to Applicants
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Closing Date: 30 November 2026
Data Protection, Privacy and Checks
The Company complies with local and international data protection and privacy legislation. This includes transparency in the processing of personal information processed about job applicants during the recruitment process. By applying for this position, applicants agree to the processing of their personal data in accordance with our recruitment procedure and Privacy Notice available from our website.
The Company may perform background, criminal and/or other relevant checks on all applicants applying for positions, as is relevant to the position.
Compensation: Competitive / Market-related – commensurate with experience and location