About Gilead Sciences

Gilead Sciences is a leading biopharmaceutical company dedicated to creating a healthier world for all people. For over 35 years, Gilead has pioneered breakthroughs in treating some of the world's most devastating diseases, including HIV, viral hepatitis, COVID-19, and cancer. The company's innovative therapies have delivered a cure for hepatitis C, revolutionary advancements in HIV treatment and prevention, and significant progress in oncology and inflammatory diseases. Headquartered in the United States, Gilead operates globally, ensuring access to life-changing medicines while fostering a collaborative, inclusive culture. As a Sr Manager, Statistical Programming, you'll contribute to Gilead's bold mission by leading data governance efforts that support clinical trials and real-world evidence (RWE) data, driving scientific innovation and regulatory compliance.

Role Overview

The Sr Manager, Statistical Programming position at Gilead Sciences is a remote role in the United States, offering the flexibility to work from anywhere while making a direct impact on global health challenges. This leadership position focuses on implementing a comprehensive data governance strategy for clinical trial and RWE data. You'll provide functional leadership to align governance practices with corporate goals, regulatory requirements, and business needs. Key areas include strategy development, compliance with international regulations, data sharing oversight, operational integration, and technology innovation. With Gilead's commitment to ethical data stewardship, this role is pivotal in ensuring data accessibility, consistency, and security across the data lifecycle.

Key Responsibilities

In this role, you'll drive strategic and operational excellence in data governance. Develop and execute a data governance strategy tailored to clinical trial and RWE data, while maintaining and improving governance processes. Ensure appropriate roles and models across the data lifecycle, from retention to destruction. Champion compliance with regulations such as EMA Policy 0070 for anonymization, Health Canada PRCI, EU CTR transparency mandates, GDPR, HIPAA, and CCPA, including cross-border transfers. Collaborate with Clinical Data Sciences (CDS), Regulatory, and Legal teams to translate these into actionable policies and SOPs.

Oversee internal and external data sharing, managing anonymization algorithms, data requests, DUAs, and risk-based reviews. Implement industry best practices from TransCelerate and PhUSE. Partner with CDS and the Gilead Data Office to embed governance in operations, define standards for data retention, archival, and re-identification risk mitigation. Support due diligence for third-party vendors. Evaluate technologies like data catalogs and lineage tools, promote FAIR principles, CDISC, OMOP, and HL7 FHIR standards. Develop request portals and wikis to enhance content dissemination and continuous learning.

Qualifications & Requirements

To succeed as Sr Manager, Statistical Programming at Gilead, candidates need a strong educational foundation: Bachelor's Degree with eight years of experience, Master's Degree with six years, or PhD/PharmD with two years. Preferred qualifications include 6+ years in pharma, biotech, or medical research; 4+ years with data; and 2+ years in data governance, clinical data management, or RWE leadership. Proficiency in programming languages such as MATLAB, SAS, R, Python, or SQL is essential, alongside intermediate skills in Smartsheet, Azure DevOps, or MS PowerApps.

A deep understanding of clinical and RWE data structures, regulatory frameworks, privacy laws like GDPR and HIPAA, and anonymization techniques is required. Familiarity with EMA Policy 0070, EU CTR, governance tools (e.g., Collibra, Informatica), and data platforms (e.g., CPRD, Aetion) is highly valued. Exceptional leadership, collaboration, communication skills, and the ability to operationalize legal requirements with a strategic, execution-focused mindset are critical. As a people leader, you'll create inclusion, model diverse teams, and empower employees.

Basic Qualifications

• Bachelor's + 8 years OR Master's + 6 years OR PhD + 2 years
• Experience in pharma/biotech

Preferred Qualifications

• Programming expertise (SAS, R, Python, SQL)
• Data governance and regulatory knowledge
• Leadership in clinical/RWE data

Benefits & Perks

Gilead Sciences offers a premium compensation package for the Sr Manager, Statistical Programming role, including an estimated salary range reflecting biopharmaceutical sector rates with a buffer for top talent. Beyond competitive pay, enjoy fully remote work across the United States, comprehensive health insurance, retirement plans, and generous paid time off. Professional development programs, leadership training, and tuition reimbursement support your growth. Gilead's inclusive culture provides wellness resources, employee assistance programs, and stock options. Join a company that values work-life balance while tackling global health challenges in HIV, oncology, and inflammatory diseases.

Career Growth

At Gilead, career advancement is a priority. As a people leader, you'll evolve the company culture, fostering inclusion and empowerment. This role offers pathways to higher leadership in data sciences, regulatory affairs, or R&D. Gilead invests in training on emerging technologies, regulatory landscapes, and leadership skills. With a track record of internal promotions, ambitious professionals thrive, contributing to innovations in HIV therapies, cancer treatments, and beyond. Network with cross-functional teams and global experts to build a lasting impact.

Why Join Gilead

Gilead Sciences stands out for its relentless drive against public health threats. Your work as Sr Manager, Statistical Programming will directly support therapies improving lives worldwide. Enjoy a collaborative environment where diverse teams innovate boldly. Remote flexibility, ethical focus, and mission-driven culture make Gilead ideal for passionate leaders. Contribute to Gilead's legacy in HIV, oncology, inflammatory diseases, and viral hepatitis while advancing your career in a premium biopharma setting.

Role FAQs

Q: Is this role fully remote? Yes, available remotely across the United States.

Q: What programming skills are needed? Proficiency in SAS, R, Python, SQL, or similar.

Q: Does it require travel? Minimal, focused on remote collaboration.

Q: What regulations will I handle? GDPR, HIPAA, EMA Policy 0070, EU CTR, and more.

Q: Is leadership experience required? Yes, with accountabilities for inclusion and team development.