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Our Oncology portfolio is dedicated to advancing the development strategy for life-saving therapies. This role sits at the heart of our clinical operations, ensuring that every trial we conduct upholds the highest standards of scientific rigor and data integrity. We are a global team committed to innovation, working across diverse cultures and geographies to bring new treatments to patients who need them most.
You will serve as a clinical development expert, providing scientific oversight for Phase 1 through Phase 3 oncology trials. Your mission is to partner with medical colleagues, clinical operations, and functional lines to execute studies that drive our development strategy forward. In this capacity, you will represent the study team in governance meetings, contribute to disease area strategy, and act as a key voice in regulatory submissions.
Your day-to-day involves setting the clinical data review strategy, analyzing emerging safety profiles in partnership with medical colleagues, and leading the collection and review of quality data. You will author critical documents such as protocols, informed consent forms, and clinical study reports, while also supporting preparations for Health Authority meetings. Beyond the science, you will champion quality and efficiency, participating in enterprise-level workgroups to optimize clinical development procedures and embracing evolving technologies to enhance our processes.
Candidates selected for this role will engage in a structured interview process designed to assess both technical expertise and cultural fit. This typically includes an initial conversation with Talent Acquisition, followed by technical deep-dives and discussions with potential peers and leadership to evaluate problem-solving capabilities and collaborative skills.
Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants. We welcome candidates regardless of race, color, religion, sex, sexual orientation, age, gender identity or expression, national origin, disability, or veteran status. We strive to create a diverse team environment where colleagues from all backgrounds can thrive.
Pfizer endeavors to make our careers website and application process accessible to all users. If you require assistance completing the application process or need an accommodation for the interview process, please contact disabilityrecruitment@pfizer.com. This channel is reserved solely for accommodation requests regarding accessibility.
As part of our commitment to transparency, Pfizer reports payments and transfers of value to health care providers as required by federal and state laws, including the Sunshine Act. Additionally, this position requires permanent work authorization in the United States, and visa sponsorship is not available.
Skills: Clinical Research, Oncology, Ich Guidelines, GCP, Fda, Ema, Microsoft Office, Scientific Software, Clinical Operations, Biostatistics.
Education: PhD in a relevant Science discipline with 2 years experience.
Work model: Hybrid
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