Arbetsbeskrivning

Avaron helps you find assignments that match your skills and ambitions. As a permanently employed consultant with us, you get competitive terms – combined with the variety and growth that a consulting career offers.

You will play a key role in securing the flow of clinical trial medication in a global pharmaceutical environment where timing, quality and precision matter every day. The assignment sits close to R&D, clinical manufacturing and supply, with responsibility for designing, planning and setting up study-specific supply chains that support new medicines through clinical development.

You will work across a broad network of internal teams and external partners, making sure supplies are available in the right quality and quantity for clinical studies around the world. The environment is fast-paced and collaborative, with many moving parts, changing study needs and high expectations on quality, delivery and risk management. If you enjoy combining structured supply chain work with meaningful impact for patients, this is a very rewarding assignment.

• You will project manage the design, planning and set-up of study supply chains to secure on-time delivery of clinical supplies.
• You will lead cross-functional collaboration and keep an ongoing dialogue with internal and external partners on study design requirements and changes that affect supply.
• You will drive the delivery of clinical supplies in a consistent and effective way, while contributing to the balance between cost and supply risk.
• You will support proactive risk management for individual studies and help mitigate issues that could affect quality or delivery.
• You will take ownership of inventory management, including rework, recalls, shelf-life extensions, expiry date management and stock destruction.
• You will manage the Interactive Response Technology (IRT) system to support demand and supply planning.
• You will work within GMP quality management systems and actively handle deviations, complaints and change controls.

• Planning and supply chain knowledge within clinical supplies, clinical studies or a similar regulated pharmaceutical environment.
• Ability to project manage study supply chains from design through delivery.
• Experience working cross-functionally with internal and external partners in a global setting.
• Good understanding of inventory management and supply risk mitigation.
• Experience using IRT systems for demand and supply planning.
• Ability to work within GMP quality management systems and handle deviations, complaints and change controls.
• You are comfortable working in a high-paced R&D environment and adapting to multiple systems.
• Strong communication, influencing, negotiation and problem-solving skills across geographical and cultural boundaries.

• Awareness of GMP and GCP.
• Knowledge of clinical development processes relevant to the supply of clinical materials.
• Lean knowledge and understanding.
• Experience handling quality events such as deviations, change controls and complaints.

• Permanent employment at Avaron AB
• Occupational pension
• Wellness allowance of SEK 5,000 per year

Selections are made on an ongoing basis – apply as soon as you can.