This is a fully remote position, open to applicants in California.

📋 Description

• Act as a key point of contact between the CCOE, cross-OpCo teams, and external clinical suppliers.

• Oversee the setup of suppliers, including purchase orders, payments, performance documentation, and ongoing process support.

• Assist in managing contract workflow activities such as routing, tracking, documentation, stakeholder follow-up, and coordination with CCOE, OpCo teams, Legal, Procurement, and external suppliers.

• Ensure effective communication, documentation, and alignment across all supplier-related activities.

• Utilize Danaher Business System tools and standard operating procedures to promote process consistency and continuous improvement.

• Work collaboratively on a global scale with EU and US teams to guarantee timely delivery and support.

• Keep abreast of GCP, global standards, and SOPs to ensure compliance with regulatory requirements for clinical studies.

⛳️ Requirements

• A Bachelor’s degree in a scientific, finance, biological, or medical science field with over 5 years of experience in a regulated environment, or another relevant degree with more than 8 years of similar experience.

• Exceptional contract negotiation skills with a proven history of successful negotiations.

• Comprehensive budgeting experience with key stakeholders in the clinical environment.

• In-depth understanding of supplier management.

• Proficiency in Microsoft Office applications, including Excel, Word, and PowerPoint.

• A proactive team player with a collaborative mindset and a commitment to building and maintaining supplier processes.

• Familiarity with GCP, global standards, and SOPs related to clinical studies.

• Previous experience in medical device, pharmaceutical, finance, or other highly regulated sectors is advantageous.