Gilead

Overview

Clinical Operations is responsible for the worldwide execution of all Phase I - IV clinical trials across all Gilead therapeutic areas. You will typically lead a team of direct and indirect reports, overseeing the successful execution of more complex studies and/or multiple studies within a program.

About Gilead

At Gilead, we’re creating a healthier world for all people. For more than 35 years, we’ve tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer – working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the globe.

Requirements & Eligibility

• BA / BS / RN with extensive relevant clinical or related experience in life sciences. Or, MA / MS / PharmD / PhD with relevant clinical or related experience in life sciences.
• Typically has a demonstrable cross-functional study management or related leadership experience in life sciences, including multiple years’ experience managing study management or project teams.
• Experience developing RFPs and selection and management of CROs or other vendors.
• Typically has multiple years’ line management experience.
• Proven ability to successfully manage clinical studies within designated program budgets and timelines.
• Prior oncology clinical trials experience with several years’ experience in the design and delivery of Phase 1 first in human (FIH) oncology clinical trials

Key Responsibilities

• Typically manages a team of direct and indirect reports, hiring, developing and retaining diverse top talent.
• Provides input into strategic and operational short- and long-range therapeutic area / functional area plans.
• Provides leadership, guidance, oversight and therapeutic expertise for the successful management of all aspects of clinical trials.
• Responsible for the strategic, operational and financial oversight of assigned program(s).
• Develops, implements, manages and ensures completion of clinical trials within designated budgets and timelines.
• Assesses, on-boards and manages contract research organizations (CROs) and other vendors.
• Leads cross-functional Study Management Teams (SMTs) and influences all relevant stakeholders.