Patient-centered Research Outcomes Research
vor 2 Monaten
**The Position**:
We advance science so that we all have more time with the people we love.
**The Opportunity**
Your responsibilities include a wide variety of contributions: partnering with key collaborators, working on the molecule portfolio, supporting specialized business areas, or contributing to key initiatives that shape our science and business environments. You may be a molecule-enabling work product leader and a PCOR Science Lead on a molecule team.
- Develop and implement fit-for purpose clinical outcomes assessment (COA) strategies for clinical studies or disease areas
- Lead and/ or support cross-functional initiatives and activities to simplify and innovate how Roche performs COA strategies, and collaborate with experts in PCOR, Product Development Operations and Data Sciences, Early Development and beyond to accelerate and deliver patient benefits faster.
- Participate in cross-industry collaborative initiatives to improve industry-level COA strategy and execution standards and practices
- Assesses the need for evidence generation and contribute to evidence generation projects in measurement science and patient experience data
- Support and/or represent PCOR and PDD across multiple functions of the Roche and Genentech global organization, which may include; Pharma Research and Early Development (pRED); Genentech Research and Early Development (gRED); Product Development (PD); Market Access, and Global Product Strategy (GPS).
**Who you are**:
- You have experience in the pharmaceutical/biotech industry, or related industry
- You have an understanding of drug development and Clinical Outcome Assessments.
- You enjoy working in a dynamic environment, solving unique challenges, and working at both a granular and big picture level.
- You’re interested in designing strategies for collecting patient perspectives in our trials, and also working in cross-functional collaborative capacity above the molecule to enable the successful execution of those strategies.
**Preferred**
- Strong stakeholder management and communication skills
- Expertise in clinical trial execution or related field such as linguistic validation, eCOA, licensing of COAs
- Expertise in patient experience data, including clinical outcome assessments and patient preference
- Experience designing systems, solutions, or processes in complex (multi-function/department) environments.
- Fluency in written and spoken English
- Ability to work across multiple cultures and countries
- Willingness to travel as required
Relocation benefits are not available for this job posting.
This is a site-based role available for Basel, Welwyn, and South San Francisco sites. The expected salary range for this position if based in South San Francisco, CA is $118,000 - $219,200. 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.
**Benefits**
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.
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