Senior Supplier Governance Manager

Job not on LinkedIn

🕒 August 4

🇺🇸 United States – Remote

💵 $134.3k - $181.7k / year

⏰ Full Time

🟠 Senior

🎲 Risk

🦅 H1B Visa Sponsor

This company has sponsored H1B visas in the past.

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Amgen

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1980

🏥 Healthcare

🧬 Biotechnology

💊 Pharmaceuticals

💰 $28.5G Post-IPO Debt on 2022-12

Healthcare • Biotechnology • Pharmaceuticals

Amgen is a global leader in biotechnology, focusing on the development and commercialization of innovative medicines made from living cells. The company aims to treat serious illnesses, often targeting diseases with limited therapeutic options. Amgen emphasizes scientific innovation and is committed to ethical research, patient safety, and environmental sustainability. It actively engages in clinical trials and is known for its contributions to the fields of cancer treatment and obesity management among others.

📋 Description

• Support Amgen-sponsored clinical trials, focusing on key programs within Global Development Operations • Oversee the performance and quality of Clinical Pharmacology CROs and laboratory suppliers • Ensure supplier alignment with Amgen’s strategy and standards • Develop strategic relationships and facilitate communication and collaboration among stakeholders • Facilitate supplier governance meetings and operating reviews • Monitor key performance indicators and manage issues • Support supplier evaluation, selection, and startup • Align supplier strategy and capabilities with business needs and priorities • Build relationships with study teams, functional leads, procurement, quality, compliance, and suppliers • Lead proactive supplier risk management at portfolio and study level • Identify, develop, and implement supplier process improvements • Standardize and align clinical trial execution across programs and portfolios • Assess and implement technologies and innovations • Lead and contribute to cross-functional initiatives and special projects • Facilitate mentoring, training, and career development of direct reports • Manage direct-report performance and feedback

🎯 Requirements

• Doctorate degree and 2 years of clinical experience, or master’s degree and 4 years, or bachelor’s degree and 6 years, or associate’s degree and 10 years, or high school diploma/GED and 12 years • BS/BA/BSc in the sciences or RN preferred • 9 years’ work experience in a life sciences or medically related field, including 6 years of biopharmaceutical clinical research experience • Clinical research experience obtained at a biotech, pharmaceutical, or CRO company • Experience with Clinical Pharmacology • Experience working in a laboratory • Experience working with and/or overseeing suppliers on clinical trials • Experience with risk management • Experience leading direct reports • Experience working in a global, matrix organization • Knowledge of Good Clinical Practices (GCP), FDA regulations and guidelines, and international regulatory requirements/guidelines • Clinical trials execution experience • Project management experience • Proficiency in proactive issue management • Experience writing and presenting clearly to Senior Management • Ability to communicate effectively with a diverse audience • Excellent interpersonal, organizational, and supervisory skills • Professional collaboration and leadership skills

🏖️ Benefits

• Comprehensive employee benefits package • Retirement and Savings Plan with generous company contributions • Group medical, dental and vision coverage • Life and disability insurance • Flexible spending accounts • Discretionary annual bonus program • Stock-based long-term incentives • Award-winning time-off plans • Flexible work models where possible • Career development opportunities • Mentoring, training, and career development for direct reports