Oncology Clinical Development Scientist – Director

🕒 May 19

🏢🏡 New York City – Hybrid

💵 $176.6k - $294.3k / year

⏰ Full Time

🔴 Lead

👔 Director

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Pfizer

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1849

💰 Post-IPO Debt on 2023-05

We’re celebrating 175 years of daring scientific innovation—and we’re not done yet. Every day, we’re channeling our passion and resources into delivering innovative therapies that change the face of healthcare. Let’s outdo yesterday.

📋 Description

• Responsible for scientific oversight, data integrity and quality of clinical trial(s) in support of the development strategy for programs within the Late-Stage Oncology portfolio • Maintains current scientific and clinical knowledge in the specific therapeutic and disease area(s) of assignment • Effectively partners with other clinical and medical colleagues, clinical operations and other functional lines for the successful implementation and execution of the clinical trial(s) within the assigned program • Authors protocols, study level informed consent documents, and contributes to authoring of IBs, site training materials, clinical study reports, regulatory responses, and other clinical and regulatory documents • Analyzes the emerging safety profile of the drug, keeping the clinical and safety colleagues informed of changes in the safety profile as they occur in the assigned trial(s) • Reviews data and presents relevant findings to appropriate teams, governance bodies, and other internal and external stakeholders

🎯 Requirements

• PhD/Pharm D in a relevant Science discipline and minimum of 5 years Clinical Research experience in industry/CRO, OR MS in a relevant Science discipline and minimum of 7 years of Clinical Research experience in industry/CRO OR BA/BS in a relevant Science discipline and minimum of 10 years Clinical Research experience in a similar role in industry/CRO • Clinical Research experience in the phase 3/pivotal space in Oncology • Solid tumor or hematology clinical trial experience • Experience leading a team • Excellent knowledge of clinical procedures, ICH guidelines, GCP and familiarity with FDA, EMA, and global regulations • Extensive understanding of related disciplines, e.g., Clinical Operations, Safety, Biostatistics, Regulatory, Study Management, Pre-clinical, Pharmacology, Quality Assurance • Experience working on large data sets • Proficiency with Microsoft Office and relevant scientific software • Effective communication, presentation, and organizational skills to ensure coordinated and timely delivery • Experience leveraging a variety of communication tools and techniques to communicate results • Experience solving problems collaboratively and handling conflict constructively • Track record of scientific productivity as evidenced by publications, posters, abstracts and/or presentations • Experience working proactively and independently, organizing tasks, time and priorities of self and others • Experience building partnerships across the company to achieve the needs of the program.

🏖️ Benefits

• 401(k) plan with Pfizer Matching Contributions and additional Pfizer Retirement Savings Contribution • Paid vacation, holiday and personal days • Paid caregiver/parental and medical leave • Health benefits to include medical, prescription drug, dental and vision coverage • Participation in Pfizer’s Global Performance Plan with a bonus target of 20.0% of the base salary • Eligibility to participate in our share based long term incentive program