Pfizer

Oncology Clinical Development Scientists (Senior Manager)

Pfizer$139K — $231K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • PhD/Pharm D in relevant Science discipline with 2 years Clinical Research experience, OR MS with 3 years experience, OR BA/BS with 4 years experience in a similar role.
  • Experience in Phase 1 - 3 clinical trials in Oncology, particularly from the sponsor's perspective.
  • Strong knowledge of ICH guidelines, GCP, FDA, EMA and global regulations.
  • Experience managing large data sets as part of clinical research.
  • Proficient in Microsoft Office and relevant scientific software.

Responsibilities

  • Serve as the clinical development expert for assigned oncology studies.
  • Collaborate effectively with clinical and medical colleagues, and operational teams for trial execution.
  • Ensure scientific oversight and maintain data integrity and quality for clinical trials.
  • Represent the study team in governance meetings; support strategy discussions with the Development lead/Medical Director.
  • Author and contribute to various clinical documents and regulatory submissions.
  • Lead strategy for clinical data review and analysis.
  • Work closely with medical colleagues to assess and communicate the evolving safety profile of trial drugs.

Benefits

  • Hybrid work model requiring on-site attendance approximately 2.5 days a week.
  • 401(k) plan with matching contributions and additional retirement savings contributions.
  • Paid vacation, holidays, and personal days.
  • Comprehensive health benefits, including medical, prescription drug, dental, and vision coverage.
  • Paid caregiver, parental, and medical leave.
Full Job Description
POSITION SUMMARY

You will be responsible for scientific oversight, data integrity and quality of clinical trial(s) in support of the development strategy for programs within our Oncology portfolio.

KEY RESPONSIBILITIES
  • Clinical development expert for assigned studies maintaining current scientific and clinical knowledge in the specific therapeutic and disease area(s) of assignment.
  • Effectively partner 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.
  • Responsible for scientific oversight, data integrity and quality of the clinical trial(s).
  • Represent the study team in governance meetings and submissions, partners with/supports the Development lead/Medical Director regarding study and disease area strategy.
  • Author 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; supports preparations for Health Authority meetings, participates as appropriate.
  • Set the clinical data review strategy and leads the team in the collection of quality data and review of emerging clinical data and trends; reviews and queries data; presents and discusses relevant data to appropriate teams, governance bodies, and other internal and external stakeholders.
  • In close partnership with medically qualified colleague/s, analyze 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).
  • Follow relevant SOPs and regulations, has an excellent understanding of and complies with applicable trainings, seeks opportunities to further improve quality and efficiency of clinical procedures; leads or actively participates in portfolio- and enterprise level workgroups aimed at optimizing PFE clinical development procedures; may be a subject matter expert or business process owner for a relevant SOP or procedure.


MINIMUM QUALIFICATIONS
  • PhD/Pharm D in a relevant Science discipline and minimum of 2 years Clinical Research experience in industry/CRO, OR
  • MS in a relevant Science discipline and minimum of 3 years of Clinical Research experience in industry/CRO OR
  • BA/BS in a relevant Science discipline and minimum of 4 years Clinical Research experience in a similar role in industry/CRO
  • Clinical Research experience in the Phase 1 - 3 space in Oncology, ideally on the side of the sponsor and with a track record of successful regulatory submission, inspection, and regulatory approval
  • 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


Candidate demonstrates a breadth of diverse leadership experiences and capabilities including: the ability to influence and collaborate with peers, develop and coach others, oversee and guide the work of other colleagues to achieve meaningful outcomes and create business impact.

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

Candidate demonstrates a breadth of diverse leadership experiences and capabilities including: the ability to influence and collaborate with peers, develop and coach others, oversee and guide the work of other colleagues to achieve meaningful outcomes and create business impact.
Work Location Assignment: Hybrid
The annual base salary for this position ranges from $139,100.00 to $231,900.00. In addition, this position is eligible for participation in Pfizer's Global Performance Plan with a bonus target of 17.5% of the base salary and eligibility to participate in our share based long term incentive program. We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of life's moments. Benefits offered include a 401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution, paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage. Learn more at Pfizer Candidate Site - U.S. Benefits | (uscandidates.mypfizerbenefits.com). Pfizer compensation structures and benefit packages are aligned based on the location of hire. The United States salary range provided does not apply to Tampa, FL or any location outside of the United States.
Relocation assistance may be available based on business needs and/or eligibility.

Medical

About Pfizer

Hospira, Inc. is the provider of injectable drugs and infusion technologies. Through its broad, integrated portfolio, Hospira is uniquely positioned to Advance Wellness™ by improving patient and caregiver safety while reducing healthcare costs. The company is headquartered in Lake Forest, Ill., and has approximately 16,000 employees.

Pfizer Careers

Joining Pfizer’s global team offers more than just job opportunities; it’s a chance to be a part of a company that leads with science and innovates for better health. As a leading biopharmaceutical company, Pfizer is at the forefront of transforming lives through innovation, leadership, and diversity. Work You’ll Do At Pfizer, you will collaborate with some of the brightest minds in the industry, engaging in work that enhances global health and saves lives. Our culture thrives on intellectual curiosity, professional growth, and inclusivity, making every day a learning opportunity. Here, your skills will be honed, your professional acumen will be expanded, and you will be part of a team that values the power of diverse insights to drive success. Pfizer’s Leadership and Growth Lead and innovate with Pfizer, where we value the growth of each employee. Our leadership is committed to providing employees with the training and resources needed to excel in their careers. Pfizer offers a variety of career paths, including roles in research, marketing, finance, technology, and more, each offering a unique blend of challenges and rewards. Internship and Employment Opportunities Start your career with Pfizer through our internship programs or dive straight into a full-time position. We are hiring individuals who are passionate about healthcare and who seek to make a difference in the world. Our internships provide invaluable industry experience, networking opportunities, and a potential pathway to full-time employment. Benefits and Culture Pfizer is dedicated to fostering a workplace where all employees feel valued and can achieve their full potential. We offer competitive benefits packages that support the health, well-being, and financial security of our employees and their families. At Pfizer, you’ll find a culture that encourages collaboration, innovation, and continuous learning. Join Our Team Explore the numerous job opportunities at Pfizer by searching open positions that match your skills and interests. We look for driven, curious, and innovative team players who are ready to advance their careers in a transformative company. Stay Connected Keep up to date with career tips, insider perspectives, and industry-leading insights you can put to use today—all from the people who work here. Personalize your subscription to receive job alerts, latest news, and insider tips tailored to your preferences. Discover the exciting and rewarding career opportunities that await at Pfizer. Interview and Resume Tips Prepare for your future with Pfizer by utilizing our resources for resume building and interview preparation. We provide guidance on how to effectively showcase your skills and experiences to align with the needs of a position at Pfizer. Our goal is to help you succeed in securing a role that suits your professional goals and personal growth aspirations. Pfizer: A Place Where You Can Make a Difference Every position at Pfizer contributes to our mission of making the world a healthier place. Whether through direct patient care, research innovation, or corporate roles that support our operations, your work will have global impact. Join us in our journey to change lives—explore Pfizer careers today.
Learn more about Pfizer
Size
79,000 employees
Market Cap
$285.9 billion
Industry
Net Income
$9.6 billion
Founded
1849
5 Year Trend
+9%
Revenue
$41.9 billion
NASDAQ

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