The Late-Stage Clinical Scientist (non-MD, Sr. Manager) is responsible for providing support of scientific oversight, data integrity and quality of clinical trial(s) in support of the development strategy for programs within the Late-Stage Oncology portfolio.

Job Responsibilities

• Clinical development professional maintaining current scientific and clinical knowledge in the specific therapeutic and disease area(s) of assignment.

• 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.

• Responsible for scientific oversight, data integrity and quality of the clinical trial(s).

• 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; supports preparations for Health Authority meetings, participates as appropriate.

• Reviews and queries safety and efficacy data in support of the clinical data review strategy and collection of quality data and review of emerging clinical data and trends; presents and discusses relevant data to appropriate teams, governance bodies, and other internal and external stakeholders.

• In close partnership with medically qualified colleague/s, 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).

• Follows 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.

• May supervise, mentor, and/or develop others.

Qualifications/Skills

• Science degree (PhD, PharmD, or equivalent) and minimum of 2-year Clinical Research experience in industry/CRO, OR BA/BS and minimum of 7-year 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.

• Excellent knowledge of clinical procedures, ICH guidelines, GCP and familiarity with FDA, EMA, and global regulations.

• Demonstrates a passion for helping patients with cancer and for the science of oncology.

• Proven analytical skills with the ability to work on large data sets.

• Effective communication, presentation, and organizational skills to ensure coordinated and timely delivery.

• Demonstrated scientific writing skills and excellent communication skills (written and spoken) in English; scientific productivity via publications, posters, abstracts and/or presentations.

• 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; works effectively with internal and external partners and investigators/medical professionals.

• Has solid understanding of related disciplines, e.g., clinical operations, safety, biostatistics, regulatory, study management, pre-clinical, pharmacology, quality assurance.

• Proficient with basic IT; efficiently using a computer and telecommunications (voice and video)

• Has the flexibility to adapt and navigate through an ever-changing work environment while maintaining integrity and quality in the work assigned.

• Must have the relevant personality features and competencies supporting the responsibilities:

• Demonstrates effective problem-solving, and agile decision-making in execution of Clinical responsibilities.

• Leverages knowledge and support from others related to overall objectives, strategy, critical issues, and policies.

• Embraces evolving technologies and adopts best practices aimed at improving the efficiency and quality of clinical development.

• Promotes team health and exemplifies Pfizer's leadership behaviors and actionable attitudes.

• Has foresight and judgment in complex decisions:

• Leverages a variety of communication tools and techniques to communicate results.

• Builds partnerships across the company to achieve the needs of the program.

• Collaborative problem solving (handles conflict constructively)

• Promotes innovation and takes appropriate risks to challenge the status quo to enhance the efficiency of current processes.

• Ability to work proactively and independently, organize tasks, time and priorities of self and others.

• 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 - must be onsite an average of 2.5 days/week

PHYSICAL/MENTAL REQUIREMENTS

need to be able to work from a computer, work on a team

NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS

40 hr week needs to be able to work east coast/west coast/EU hours depending on team

#LI-PFE

The annual base salary for this position ranges from $131,200.00 to $218,600.00. 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.

Sunshine Act

Pfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations. These laws and regulations require Pfizer to provide government agencies with information such as a health care provider's name, address and the type of payments or other value received, generally for public disclosure. Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act. Therefore, if you are a licensed physician who incurs recruiting expenses as a result of interviewing with Pfizer that we pay or reimburse, your name, address and the amount of payments made currently will be reported to the government. If you have questions regarding this matter, please do not hesitate to contact your Talent Acquisition representative.

EEO & Employment Eligibility

Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status. Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA. Pfizer is an E-Verify employer. This position requires permanent work authorization in the United States.

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