Associate Director - Lifecycle Management

Associate Director - Lifecycle Management

VCLS - Voisin Consulting Life Sciences

Copenhagen, Denmark

This role will see you thrive at the intersection of science, strategy, and client relationships. As an experienced Regulatory Scientist with a consulting mindset, you’ll play a pivotal role in the life cycle management (LCM) of cutting-edge biotech and pharma products. You’ll bring your expertise, leadership, and insight to help clients navigate complex regulatory landscapes — and deliver lasting impact across the Nordic region and beyond.

What You'll Do

Lead Regulatory and LCM Strategy

• Act as a key technical and strategic advisor to life science clients, focusing on Nordic regulatory requirements;
• Provide actionable, evidence-based recommendations that influence regulatory outcomes;
• Ensure compliance and innovation go hand in hand, staying ahead of global and local trends.

Drive Client Success

• Cultivate long-term partnerships by building trust from first conversation to final delivery;
• Translate complex regulatory issues into business-savvy solutions;
• Proactively identify opportunities to expand our impact with Nordic clients.

Project Leadership with Precision

• Lead cross-functional teams and manage end-to-end delivery of regulatory projects;
• Own project timelines, scope, and budget - and deliver with excellence;
• Mentor and support fellow consultants to elevate team performance.

What You Bring

• 10+ years in Regulatory Affairs, with solid experience as a consultant;
• Proven expertise in Nordic and global regulatory frameworks (EMA, FDA, local authorities);
• Strong consulting mindset with the ability to advise, lead, and influence;
• A well-established industry network and the confidence to engage with senior stakeholders;
• Skilled in project management, client development, and mentoring.

Requirements

• Advanced degree in life sciences, pharmacy, medicine, or related field;
• Experience in project management, including resource orchestration, workload and budget management;
• Proven consulting and client-facing experience in the life sciences sector.

Skills

• Deep understanding of global regulatory frameworks (e.g., FDA, EMA, local Nordic country-level);
• Strategic, analytical, and detail-oriented with a strong business mindset;
• Ability to leverage an existing network within the biotech/pharma industry and to interface with clients from generating the business up to delivery;
• Proficiency in working across emerging markets and diverse organizational structures;
• Confident in complex, matrixed, and international environments;
• Proactive, resilient, empathetic, influential, and organizationally agile.