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Global Clinical Operations (PDG) aims to enhance strategic decision-making and foster accountability to promote a culture of responsibility and ownership. We focus on collective guidance to ensure alignment and cohesive efforts, along with establishing consistent processes and approaches across TAs and CODACs. Additionally, PDG seeks to strengthen external engagement with partners and foster collaborative partnerships. By concentrating on these areas, we aim to create an environment where teams and individuals feel excited, confident, and supported in their work.
The Opportunity:
As a Centers of Excellence (CoE) Lead within PDG, your primary focus will be on driving impact to enhance productivity and facilitating the delivery of clinical trials to patients.
You will contribute and enable innovative clinical trial delivery and address emergent, high-impact needs that arise across multiple Clinical Operations Disease Area Communities (CODACs) to enable more efficient, seamless clinical trial delivery for patients, investigators, and clinical site staff.
With minimal guidance will maintain a global reach to support local business needs and achieve cross-country alignment, ensuring individuals within PDG have a clear understanding of their roles and responsibilities.
Foster a culture that values collective success and high performance, ultimately benefiting patients.
Collaborate with Quality and Compliance experts to eliminate duplication, clarify roles, and establish a strong first line of defense for compliance and quality assurance.
Be accountable for GCP/GVP compliance, business process owner, data integrity, and take a balanced risk-based approach in your work, seeking guidance or direction as needed.
Support new ways of working for example to use data, AI, and innovative technologies to propel the business forward.
Who You Are:
Bachelor's degree in Life Sciences or related field.
4+ years of relevant experience in clinical trial operations in process.
4+ years of relevant experience or in compliance/audit and inspections
4+ years of relevant experience in vendor management or systems and learning.
Preferred Qualifications:
Has a strong knowledge of the role of clinical operations in product development; is aware of the clinical operations industry.
Independently prioritizes their own work and effectively influences the team to develop plans for implementing clinical trial infrastructure projects.
Developing leadership skills, mentoring and coaching colleagues with less experience, and provide guidance; may lead parts of projects.
Solves complex outcomes; takes a new perspective on existing solutions; exercises judgment based on analyzing multiple sources of information and advice. Is able to engage the right partners.
Relocation benefits are not available for this job posting.
The expected salary range for this position based on the primary location of South San Francisco, CA is $.00 - $.00 USD Annual. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law. A discretionary annual bonus may be available based on individual and Company performance. This position also qualifies for the benefits detailed at the link provided below.
Genentech is an equal opportunity employer, and we embrace the increasingly diverse world around us. Genentech prohibits unlawful discrimination based on race, color, religion, gender, sexual orientation, gender identity or expression, national origin or ancestry, age, disability, marital status and veteran status.