# Clinical Research Scientist **Company**: Pfizer **Location**: New York City, New York **Work arrangement**: hybrid **Experience**: senior **Job type**: full-time **Salary**: $176,600.00 to $294,300.00 **Category**: Healthcare **Industry**: Healthcare **Apply**: https://pfizer.wd1.myworkdayjobs.com/en-US/PfizerCareers/job/United-States---New-York---New-York-City/Oncology-Late-Stage-Clinical-Development-Scientist--Non-MD---Multiple-Openings--Director_4966622-1?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply **Canonical**: https://yubhub.co/job/clinical-research-scientist-2ff77ec6-d95/ ## Description You will be responsible for scientific oversight, data integrity and quality of clinical trials in support of the development strategy for programs within the Late-Stage Oncology portfolio. **Key Responsibilities** - Provide clinical development expertise for assigned studies, maintaining current scientific and clinical knowledge in the specific therapeutic and disease area(s) of assignment. - Partner with other clinical and medical colleagues, clinical operations and other functional lines for successful implementation and execution of clinical trials. - Ensure scientific oversight, data integrity and quality of clinical trials. - Represent the study team in governance meetings and submissions, and support the Development lead/Medical Director regarding study and disease area strategy. - Author protocols, study level informed consent documents, and contribute to authoring of IBs, site training materials, clinical study reports, regulatory responses, and other clinical and regulatory documents. - Set the clinical data review strategy and lead the team in collecting quality data and reviewing emerging clinical data and trends. - Analyze the emerging safety profile of the drug, keeping clinical and safety colleagues informed of changes in the safety profile. - Follow relevant SOPs and regulations, and seek opportunities to improve quality and efficiency of clinical procedures. **Minimum Qualifications** - 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, ideally on the side of the sponsor and with a track record of successful regulatory submission, inspection, and regulatory approval - 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 **Competencies for Success** - Demonstrates passion for helping patients with cancer and for the science of oncology - Flexibility to adapt and navigate through an ever-changing work environment while maintaining integrity and quality in the work assigned - Demonstrates autonomous delivery, problem-solving, and agile decision-making in execution of Clinical responsibilities - Promotes team health and exemplifies Pfizer’s leadership behaviors and actionable attitudes - Leverages knowledge and support from others related to overall objectives, strategy, critical issues, and policies - Demonstrates foresight and judgment to make complex decisions - Promotes innovation and takes appropriate risks to challenge the status quo in order to enhance the efficiency of current processes - Embraces evolving technologies and adopts best practices aimed at improving the efficiency and quality of clinical development - Has a global perspective and mindset. Works well in a diverse team environment with colleagues from diverse cultures, backgrounds, and geographies. both as a leader and a key contributor **Work Location Assignment:** This is a hybrid role requiring you to live within commuting distance and work on-site an average of 2.5 days per week. The annual base salary for this position ranges from $176,600.00 to $294,300.00. In addition, this position is eligible for participation in Pfizer’s Global Performance Plan with a bonus target of 20.0% of the base salary and eligibility to participate in our share based long term incentive program. For more fresh new jobs, check out [yubhub.co](https://yubhub.co/). ## Skills ### Required - Clinical Research - Oncology - GCP - ICH guidelines - FDA - EMA - Microsoft Office - scientific software --- Source: [Apply at pfizer.wd1.myworkdayjobs.com](https://pfizer.wd1.myworkdayjobs.com/en-US/PfizerCareers/job/United-States---New-York---New-York-City/Oncology-Late-Stage-Clinical-Development-Scientist--Non-MD---Multiple-Openings--Director_4966622-1?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)