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ProductLife Group (PLG) is seeking an Associate Consultant to support data readiness, system implementation, and evidence generation for European regulatory and market access initiatives. You will work with experts, contribute to multiple digital and Life Sciences projects, and gradually take ownership of analyses, deliverables, and client communications.
Hybrid role based in Copenhagen with three days on-site and travel to client sites as needed; you will develop consulting skills, expand your
ProductLife Group (PLG) is a global Life Sciences consulting and outsourcing company providing expert services in Product Development, Market and Patient Access, Regulatory Affairs, Safety & Vigilance, Engineering, and Digital Transformation. Headquartered in Paris, the Group operates internationally through affiliates worldwide, with teams across North America, Europe, and APAC.
ProductLife Group (PLG) is a global Life Sciences consulting and outsourcing company providing expert services in Product Development, Market and Patient Access, Regulatory Affairs, Safety & Vigilance, Engineering, and Digital Transformation. Headquartered in Paris, the Group operates internationally through affiliates worldwide, with teams across North America, Europe, and APAC.
Behind every new medicine are systems and data that must be right: the lab data that supports the science, the clinical and regulatory systems that carry a product to approval, and the evidence that decides whether patients across Europe get access to it. At PLG, our digital team helps global pharma and biotech companies get this right.
As an Associate Consultant, you will work alongside experienced experts on projects that matter to our clients and, ultimately, to patients. You will contribute to a variety of digital and Life Sciences initiatives, supporting and progressively taking ownership of activities ranging from data readiness and system implementation to evidence generation and AI-enabled solutions. You might prepare data for a new laboratory system, support the rollout of regulated platforms, or help build evidence for the new EU Joint Clinical Assessments (JCA). Through structured coaching, hands-on project experience, and close collaboration with senior colleagues, you will develop your consulting skills, deepen your industry knowledge, and gradually expand your responsibilities.
Deliver data readiness, cleansing, mapping, and migration activities for laboratory, clinical, regulatory, and related systems.